Adiponectin and Adiponectin Receptors
http://www.100md.com
内分泌进展 2005年第3期
Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan
Department of Integrated Molecular Science on Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan
Core Research for Evolutional Science and Technology of Japan Science and Technology Agency, Kawaguchi 332-0012, Japan
Abstract
Metabolic syndrome is thought to result from obesity and obesity-linked insulin resistance. Obesity in adulthood is characterized by adipocyte hypertrophy. Adipose tissue participates in the regulation of energy homeostasis as an important endocrine organ that secretes a number of biologically active "adipokines."
Heterozygous peroxisome proliferator-activated receptor- knockout mice were protected from high-fat diet induced obesity, adipocyte hypertrophy, and insulin resistance. Systematic gene profiling analysis of these mice revealed that adiponectin/Acrp30 was overexpressed. Functional analyses including generation of adiponectin transgenic or knockout mice have revealed that adiponectin serves as an insulin-sensitizing adipokine. In fact, obesity-linked down-regulation of adiponectin was a mechanism whereby obesity could cause insulin resistance and diabetes.
Recently, we have cloned adiponectin receptors in the skeletal muscle (AdipoR1) and liver (AdipoR2), which appear to comprise a novel cell-surface receptor family. We showed that AdipoR1 and AdipoR2 serve as receptors for globular and full-length adiponectin and mediate increased AMP-activated protein kinase, peroxisome proliferator-activated receptor- ligand activities, and glucose uptake and fatty-acid oxidation by adiponectin. Obesity decreased expression levels of AdipoR1/R2, thereby reducing adiponectin sensitivity, which finally leads to insulin resistance, the so-called "vicious cycle." Most recently, we showed that osmotin, which is a ligand for the yeast homolog of AdipoR (PHO36), activated AMPK via AdipoR in C2C12 myocytes. This may facilitate efficient development of adiponectin receptor agonists.
Adiponectin receptor agonists and adiponectin sensitizers should serve as versatile treatment strategies for obesity-linked diseases such as diabetes and metabolic syndrome.
I. Introduction
II. Identification and Molecular Structure
A. Identification
B. Molecular structure and multimeric form of adiponectin
III. Adiponectin and Insulin Resistance
A. Low plasma adiponectin levels and insulin resistance
B. Insulin-sensitizing effects of adiponectin
IV. Mouse Models
V. Mechanism of Action of Adiponectin
A. Insulin-sensitizing actions
B. Antiatherosclerotic actions
VI. Alterations in Adiponectin Gene Are Associated with Human Diabetes
VII. Cloning of Adiponectin Receptors AdipoR1 and AdipoR2
VIII. Regulation of Adiponectin Receptors
A. Regulation of expression levels of AdipoR1 and AdipoR2
IX. Adiponectin Hypothesis
X. Adiponectin and Adiponectin Receptors as Therapeutic Targets
A. Up-regulation of plasma adiponectin
B. Up-regulation of adiponectin receptors and development of AdipoRs agonists
C. Pleiotropic effects of adiponectin in relation to metabolic syndrome
I. Introduction
HIGH-FAT (HF) diet-induced insulin resistance associated with obesity is a major risk factor for diabetes and cardiovascular diseases, the prevalence of which is increasing sharply (1, 2). However, the molecular basis for this association remains to be elucidated. The adipose tissue itself serves as the site of triglyceride (TG) storage and free fatty acid/glycerol release in response to changing energy demands (1). Adipose tissue also participates in the regulation of energy homeostasis as an important endocrine organ that secretes a number of biologically active adipokines such as free fatty acid (3), adipsin (4), leptin (5), plasminogen activator inhibitor-1 (6), resistin (7), and TNF- (8). Adiponectin is one such adipokine that has recently attracted much attention. In this review, we will describe recent progress made in adiponectin research with particular emphasis on the role of adiponectin in the regulation of insulin sensitivity and the development of insulin resistance. Other aspects of adiponectin research have been reviewed elsewhere (9, 10, 11, 12, 13, 14).
II. Identification and Molecular Structure
A. Identification
Adiponectin was originally identified independently by four groups using different approaches. Mouse cDNAs for adiponectin, termed Acrp30 (15) and AdipoQ (16), were cloned by differential display before and after differentiation of mouse 3T3-L1 and 3T3-F442A cells. Human adiponectin cDNA was isolated by large-scale random sequencing of a 3'-directed human adipose tissue cDNA library (17). Human adiponectin was also purified from plasma as a gelatin binding protein, GBP28 (18).
B. Molecular structure and multimeric form of adiponectin
Adiponectin structurally belongs to the complement 1q family (19, 20, 21) (Fig. 1) and is known to form a characteristic homomultimer (22) (Fig. 2). It has been demonstrated that simple SDS-PAGE under nonreducing and non-heat-denaturing conditions clearly separates multimeric species of adiponectin (23) (Fig. 2). Adiponectin in human or mouse serum and adiponectin expressed in NIH-3T3 cells or Escherichia coli forms a wide range of multimers from trimers and hexamers to high molecular weight (HMW) multimers (23) such as dodecamers and 18 mers, as demonstrated by ourselves and other groups (22, 24, 25) (Fig. 2).
Adiponectin can exist as full-length or a smaller, globular fragment; however, almost all adiponectin appears to exist as full-length adiponectin in plasma. Lodish’s group reported that a small amount of globular adiponectin was detected in human plasma (26) (Fig. 1). It has been proposed that the globular fragment is generated by proteolytic cleavage, and recently it has been shown that the cleavage of adiponectin by leukocyte elastase secreted from activated monocytes and/or neutrophils could be responsible for the generation of the globular fragment of adiponectin (27). However, the pathophysiological importance of adiponectin cleavage by leukocyte elastase in vivo remains to be determined.
Oligomer formation of adiponectin depends on disulfide bond formation mediated by Cys-39 (28). Interestingly, a mutant adiponectin with a substitution of Cys by Ser at codon 39, which formed a trimer and readily underwent proteolytic cleavage, showed much more potent bioactivity, such as reduction of glucose output from primary hepatocytes, than wild-type adiponectin with a HMW.
Hydroxylation and glycosylation of the four lysines in the collagenous domain of adiponectin have been shown to play important roles in enhancing the ability of subphysiological concentrations of insulin to inhibit gluconeogenesis in hepatocytes (29). Adiponectin was reported to be an 2,8-linked disialic acid-containing glycoprotein, although the biological functions of the disialic acid epitope of adiponectin remain to be elucidated (30).
III. Adiponectin and Insulin Resistance
A. Low plasma adiponectin levels and insulin resistance
Spiegelman’s group reported that adiponectin expression is exclusive to adipose tissue and that the mRNA expression of adiponectin was reduced in obese diabetic murine model db/db mice (16). Plasma levels of adiponectin have also been reported to be significantly reduced in obese/diabetic mice and humans (16, 31, 32). Moreover, plasma adiponectin levels have been shown to be decreased in patients with cardiovascular diseases (33, 34), hypertension (35), or metabolic syndrome (36). Thus, reductions in plasma adiponectin levels are commonly observed in a variety of states frequently associated with insulin resistance. However, whether this apparent parallelism between low plasma adiponectin levels and insulin resistance represents a cause and effect relationship was not known.
B. Insulin-sensitizing effects of adiponectin
The insulin-sensitizing effect of adiponectin was first identified by three independent groups in 2001 (26, 31, 37). We previously generated heterozygous PPAR (peroxisome proliferator-activated receptor) knockout mice that remained insulin-sensitive on a HF diet (38). In an attempt to identify insulin-sensitizing molecules secreted from white adipose tissue of heterozygous PPAR knockout mice, oligonucleotide microarray analysis was carried out using white adipose tissue (39). Adiponectin as well as leptin expression was up-regulated. Leptin was previously shown to be a major insulin-sensitizing adipokine (40).
To verify the direct insulin-sensitizing effect of adiponectin in vivo, an insulin-resistant lipoatrophic diabetic mouse model that displays both adiponectin and leptin deficiency was employed (41). Replenishment of a physiological dose of recombinant adiponectin to the lipoatrophic diabetic mice significantly ameliorated insulin resistance (31). Moreover, insulin resistance in lipoatrophic mice was completely reversed by the combination of physiological doses of adiponectin and leptin, but only partially by either adiponectin or leptin alone (31). These data clearly indicate that adiponectin has a direct insulin-sensitizing action. These data also suggest that leptin and adiponectin may be the two major insulin-sensitizing hormones secreted from adipose tissue.
We also studied whether adiponectin can improve insulin resistance and diabetes in murine models of type 2 diabetes, characterized by obesity, insulin resistance, and hyperglycemia. Serum adiponectin levels were decreased in KKAy mice on a HF diet compared with those under a high-carbohydrate diet (31) (Fig. 3). Lower serum adiponectin levels in KKAy mice on the HF diet were partially restored by replenishment of recombinant adiponectin. Importantly, replenishment of adiponectin significantly ameliorated HF diet-induced insulin resistance and hypertriglyceridemia (31) (Fig. 3). These data suggest that the insulin resistance associated with HF diets and obesity is caused at least in part by the decreases in adiponectin linked to those circumstances. The data suggest that the fat-derived hormone adiponectin is decreased in obesity and deficient in lipoatrophy, and that reduction in adiponectin plays causal roles in the development of insulin resistance in these models.
Scherer’s group has reported that an acute increase in circulating adiponectin levels triggers a transient decrease in basal glucose levels by inhibiting both the expression of hepatic gluconeogenic enzymes and the rate of endogenous glucose production in both wild-type mice and a type 2 diabetes mouse model (37, 42), consistent with the proposal that adiponectin sensitizes the body to insulin. Lodish’s group reported that a proteolytic cleavage product of adiponectin increases fatty-acid oxidation in muscle and causes a decrease in plasma glucose and weight loss in mice (26).
These data raise the possibility that the replenishment of adiponectin may provide a novel treatment modality for insulin resistance and type 2 diabetes.
IV. Mouse Models
The chronic effects of adiponectin on insulin resistance in vivo were investigated by generating globular adiponectin transgenic mice (43, 44) or adiponectin-deficient mice (45, 46, 47). Globular adiponectin transgenic mice were generated and crossed with ob/ob mice (45). Globular adiponectin transgenic ob/ob mice showed partial amelioration of insulin resistance and diabetes, but not of obesity (43). These data suggested that chronic elevation of globular adiponectin has a direct insulin-sensitizing effect independent of white adipose tissue mass.
Scherer’s group reported that transgenic mice with a deletion in the collagenous domain of adiponectin displayed 3-fold elevated levels of circulating adiponectin, raised lipid clearance and lipoprotein lipase activity, and improved insulin-mediated suppression of endogenous glucose production, thereby improving insulin sensitivity (44). In rats, sustained peripheral expression of adiponectin by the transgene also offset the development of diet-induced obesity (48).
Globular adiponectin transgenic mice were also crossed with apolipoprotein E (apoE)-deficient mice to study whether globular adiponectin can inhibit atherosclerosis in vivo (43). apoE-Deficient mice are hypercholesterolemic and spontaneously develop severe atherosclerosis. We compared the extent of atherosclerotic lesions of globular adiponectin transgenic apoE-deficient mice to that in control apoE-deficient mice. Although serum parameters such as total cholesterol, TG, glucose, and insulin were not altered, the en face Sudan IV-positive lesion areas of the arch and the descending aorta were significantly smaller in globular adiponectin transgenic apoE-deficient mice than in control apoE-deficient littermates (43). Similar results were obtained by using adenoviral-mediated overexpression of adiponectin in apoE knockout mice (49). Thus, overexpression of adiponectin resulted in marked reduction of atherosclerotic lesion formation. Together with the observations that adiponectin can ameliorate diabetes and hyperlipidemia, adiponectin can reduce atherosclerosis both via direct effects on vascular wall and via reduction in risk factors.
To determine the physiological role of adiponectin, we and others have generated adiponectin knockout mice and reported that adiponectin-deficient mice exhibited characteristics of the metabolic syndrome such as insulin resistance, glucose intolerance, hyperlipidemia, and hypertension (35, 45, 46).
We and others also studied the role of adiponectin in vascular wall using adiponectin knockout mice (45, 50). We placed a cuff around the femoral artery to induce inflammation of the adventitia and subsequent neointimal formation 2 wk after cuff placement. Intimal thickness was significantly greater (2-fold) in adiponectin knockout mice than in the wild-type mice. Thus, adiponectin plays a protective role against neointimal formation in response to injury (45, 50).
V. Mechanism of Action of Adiponectin
A. Insulin-sensitizing actions
1. Adiponectin reduces tissue TG content and up-regulates insulin signaling.
Interestingly, in skeletal muscle, adiponectin increased expression of molecules involved in fatty-acid transport such as CD36, in combustion of fatty-acid such as acyl-coenzyme A oxidase, and in energy dissipation such as uncoupling protein 2. These changes led to decreased tissue TG content in skeletal muscle (31).
Increased tissue TG content has been reported to interfere with insulin-stimulated phosphatidylinositol (PI) 3-kinase activation and subsequent glucose transporter 4 translocation and glucose uptake, leading to insulin resistance (3). Thus, decreased tissue TG content in muscle may contribute to improved insulin signal transduction. This was demonstrated in skeletal muscle of lipoatrophic mice treated with adiponectin, in which increases in insulin-induced tyrosine phosphorylation of insulin receptor and insulin receptor substrate-1 and insulin-stimulated phosphorylation of Akt were seen (31).
2. Adiponectin activates PPAR.
Based on the data that treatment of lipoatrophic or obese diabetic mice with adiponectin or overexpression of adiponectin in ob/ob mice resulted in increased expression levels of PPAR target genes such as CD36, acyl-coenzyme A oxidase, and uncoupling protein 2, we hypothesized that adiponectin could activate PPAR (31) (Fig. 4).
Consistent with this hypothesis, adiponectin indeed increased the expression levels of PPAR in vivo (31). These data suggested that adiponectin increased fatty-acid combustion and energy consumption, presumably via PPAR activation at least in part, which led to decreased TG content in the liver and skeletal muscle and thus coordinately increased in vivo insulin sensitivity.
Endogenous PPAR ligand activities were measured in vitro to further clarify the mechanisms by which adiponectin activated PPAR (31, 43). Interestingly, the treatment of C2C12 myocytes with adiponectin for 6 h significantly increased PPAR ligand activities (43) and at the same time fatty-acid oxidation in vitro.
3. Adiponectin activates AMP kinase.
We next examined the effects of treatment of adiponectin for a shorter time period (51). Treatment of C2C12 myocytes with adiponectin for 1 h stimulated fatty-acid oxidation. Although actinomycin D had no effect on the increase in fatty-acid oxidation stimulated by adiponectin for 1 h, it suppressed fatty-acid oxidation stimulated by the PPAR agonist Wy-14,643. Moreover, treatment of C2C12 myocytes for 1 h stimulated glucose uptake. We hypothesized that adiponectin may stimulate ?-oxidation and glucose uptake via AMP-activated protein kinase (AMPK) during a period shorter than 6 h (51).
Globular adiponectin and full-length adiponectin stimulated phosphorylation and activation of AMPK in skeletal muscle, whereas only full-length adiponectin did so in the liver (51). In parallel with its activation of AMPK, adiponectin stimulated phosphorylation of acetyl coenzyme-A carboxylase (ACC), fatty-acid combustion, glucose uptake, and lactate production in myocytes, and also stimulated phosphorylation of ACC and caused a reduction in molecules involved in gluconeogenesis in the liver, which can account for the acute glucose-lowering effects of adiponectin in vivo (51). Blocking AMPK activation by use of a dominant negative mutant inhibited each of these effects, indicating that stimulation of glucose utilization and fatty-acid combustion by adiponectin occurs through activation of AMPK. Our data may provide a novel paradigm that an adipocyte-derived hormone activates AMPK, thereby directly regulating glucose metabolism and insulin sensitivity in vitro and in vivo (51) (Fig. 4).
The group of Lodish and Ruderman also showed that the adiponectin/ACRP30 globular domain enhanced muscle fat oxidation and glucose transport via AMPK activation and ACC inhibition (52). More recently, AMPK was reported to be involved in glucose uptake stimulated by the globular domain of adiponectin in primary rat adipocytes (53). Because leptin has also been shown to stimulate AMPK in skeletal muscle (54), activation of AMPK may be a common mechanism by which insulin-sensitizing adipokines such as adiponectin and leptin increase insulin sensitivity.
Scherer’s group also reported that in adiponectin transgenic mice, reduced expression of gluconeogenic enzymes such as phosphoenolpyruvate carboxykinase and glucose-6-phosphatase was associated with elevated phosphorylation of AMPK in liver (44). The same group reported that adiponectin is found as two forms in serum, as a lower molecular weight trimer-dimer and a HMW complex (28). Female subjects display significantly higher levels of the HMW complex in serum than do male subjects (23, 28, 55, 56, 57). Levels of the HMW complex appeared to be negatively regulated by insulin. In accordance with this, the amount of HMW adiponectin complex, but not the total amount of adiponectin, was recently reported to be correlated with a thiazolidinedione-mediated improvement in insulin sensitivity (55).
B. Antiatherosclerotic actions
Adiponectin has been reported to have direct antiatherosclerotic effects (58, 59, 60, 61, 62, 63, 64, 65, 66, 67). Adiponectin was demonstrated to strongly inhibit the expression of adhesion molecules, including intracellular adhesion molecule-1, vascular cellular adhesion molecule-1, and E-selectin (Fig. 5). Adiponectin was also shown to inhibit TNF--induced nuclear factor-B activation through the inhibition of IB phosphorylation (61). Suppression of nuclear factor-B by adiponectin might be a major molecular mechanism for the inhibition of monocyte adhesion to endothelial cells (62). Adiponectin also inhibits the expression of the scavenger receptor class A-1 of macrophages, resulting in markedly decreased uptake of oxidized low-density lipoprotein by macrophages and inhibition of foam cell formation (63). In addition, in cultured smooth muscle cells, adiponectin attenuated DNA synthesis induced by growth factors including platelet-derived growth factor, heparin-binding epidermal growth factor (EGF)-like growth factor, basic fibroblast growth factor, and EGF, as well as cell proliferation and migration induced by heparin-binding EGF-like growth factor (64). This inhibition was shown to be attributable to the inhibition of signal transduction through ERK. More recently, selective suppression of endothelial cell apoptosis via AMPK activation by the HMW form of adiponectin has been reported (65).
VI. Alterations in Adiponectin Gene Are Associated with Human Diabetes
Independent of these functional analyses carried out in vitro and in animal models, data from human genetic studies on adiponectin also support the role of adiponectin as a determinant of susceptibility to insulin resistance and type 2 diabetes. By use of affected sib-pair analysis, complete genome mapping of type 2 diabetes genes in Japanese was performed (68). The genome scans revealed at least nine chromosomal regions linked to type 2 diabetes in Japanese people. Among these, three chromosomal regions (3q, 15q, and 20q) are the same regions as previously reported in other ethnic groups. Among these three chromosomal regions, interestingly, the 3q27 chromosomal region contains the adiponectin gene.
We screened for the adiponectin gene and identified 10 relatively common single nucleotide polymorphisms (SNPs) in the Japanese population (Fig. 6). One such SNP, SNP 276 in intron 2 (G vs. T), showed interesting phenotypes with respect to plasma adiponectin levels, insulin resistance, and susceptibility to type 2 diabetes (69) (Fig. 7). Subjects with the G/G genotype had lower plasma adiponectin levels than those with the T/T genotype. Subjects with the G/G genotype at position 276 had a higher insulin resistance index than those with T/T. Importantly, subjects with the G/G genotype at position 276 were at increased risk for type 2 diabetes. The odds ratio was slightly greater than 2 (69) (Fig. 8). Similar associations for the adiponectin gene with susceptibility to type 2 diabetes have also been reported in other ethnic groups (70, 71, 72). In German and American Caucasians, the SNP 276, either independently or as a haplotype together with SNP 45 in exon 2, was shown to be associated with obesity and insulin resistance (71, 72). In French Caucasians, two SNPs in the promoter region of the adiponectin gene, SNP-11377 and SNP-11391, were significantly associated with hypoadiponectinemia and type 2 diabetes (70). Taken together, these data strongly support the hypothesis that adiponectin plays a pivotal role in the pathogenesis of type 2 diabetes.
Several cross-sectional studies have reported that adiponectin levels were decreased in subjects with type 2 diabetes and are inversely correlated with insulin resistance. However, no studies had investigated whether adiponectin protects subjects from diabetes or the extent of risk of developing diabetes in subjects with hypoadiponectinemia. Recently, matched case-control studies in subjects recruited from a large cohort have examined the protective effect of adiponectin against diabetes. One study was performed in severely obese Pima Indian subjects, who have the highest known prevalence of obesity and type 2 diabetes in the world, to assess the role of adiponectin independent of the effects of obesity (73). Subjects with high concentrations of adiponectin were 40% less likely to develop type 2 diabetes than those with low concentrations after adjustment for body mass index (BMI), indicating that adiponectin could be used as a predictor of future development of type 2 diabetes in addition to the established risk parameters, such as BMI.
In addition to the relatively common SNPs, eight mutations in the human adiponectin gene have been reported (69, 74, 75), some of which were significantly related to diabetes and hypoadiponectinemia (23, 75). Among human adiponectin mutations, Arg112Cys and Ile164Thr mutants did not assemble into trimers, which caused impaired secretion from the cell (23). These mutants are clinically associated with hypoadiponectinemia. The Gly84Arg and Gly90Ser mutants were able to assemble into trimers and hexamers but were unable to form HMW multimers (the HMW multimers are thought to be larger than heximers), which are clinically associated with diabetes. These data raised the possibility that HMW multimers have more potent insulin-sensitizing effects than trimers and hexamers (23).
These data suggest that impaired multimerization of adiponectin may be among the causes of a diabetic phenotype or hypoadiponectinemia in subjects having these mutations. Thus, not only the total concentrations but also the multimer distribution should always be considered when interpreting plasma adiponectin levels in health as well as various disease states (23, 24, 25).
VII. Cloning of Adiponectin Receptors AdipoR1 and AdipoR2
We believe that cloning of the adiponectin receptor should facilitate studies on the regulation of glucose and lipid metabolism, the molecular causes of diabetes and atherosclerosis, and the development of antidiabetic and antiatherosclerotic drugs. We isolated cDNA for adiponectin receptors (AdipoR) that mediate the antidiabetic effects from human skeletal muscle cDNA library by screening for globular adiponectin binding (76).
The cDNA analyzed encoded a protein designated human AdipoR1 (Fig. 8) (76). This protein is conserved from yeast to man (especially in the seven transmembrane domains). Interestingly, this yeast homolog YOL002c plays a key role in metabolic pathways that regulate lipid metabolism such as fatty-acid oxidation (77).
Because there may be two distinct adiponectin receptors, we searched for a homologous gene in the human and mouse databases. We found only one gene that was significantly homologous (67% identity in amino acids) to AdipoR1, which was termed AdipoR2 (Fig. 8) (76). AdipoR1 was ubiquitously expressed and most abundantly expressed in skeletal muscle, whereas AdipoR2 was most abundantly expressed in mouse liver. It was reported that adiponectin receptors were expressed in pancreatic ?-cells, and that fatty acids may regulate their expression levels (78). GH is reported to be a positive regulator of AdipoR2 in 3T3-L1 adipocytes (79).
AdipoR1 and AdipoR2 appeared to be integral membrane proteins; the N terminus was internal, and the C terminus was external, which is opposite to the topology of all other reported G protein-coupled receptors (Fig. 8) (76). AdipoR1 and AdipoR2 may form both homo- and heteromultimers. Scatchard plot analysis revealed that AdipoR1 is a receptor for globular adiponectin, whereas AdipoR2 is a receptor for full-length adiponectin (76). Suppression of AdipoR1 with small interfering RNA (siRNA) reduced the increase in fatty-acid oxidation by globular adiponectin. Suppression of AdipoR2 with siRNA reduced the increase in fatty-acid oxidation by full-length adiponectin (Fig. 9) (76).
Thus, we have isolated cDNA-encoding adiponectin receptors (AdipoR1 and R2). Expression of AdipoR1/R2 or suppression of AdipoR1/R2 supports our conclusion that AdipoR1 and R2 serve as receptors for globular and full-length adiponectin and mediate increased AMPK, PPAR ligand activities and fatty-acid oxidation and glucose uptake by adiponectin (Fig. 9) (57).
Lodish’s group reported that T-cadherin was capable of binding adiponectin in C2C12 myoblasts, but not in the liver or hepatocytes (80).
VIII. Regulation of Adiponectin Receptors
A. Regulation of expression levels of AdipoR1 and AdipoR2
We first examined whether the expressions of AdipoR1 and/or AdipoR2 were regulated under physiological and/or pathophysiological states (81). The levels of AdipoR1 and AdipoR2 mRNA expression in the liver and skeletal muscle increased after fasting, and refeeding rapidly restored these to levels equal to the original fed state. AdipoR1 and AdipoR2 mRNA increased significantly in skeletal muscle of mice rendered hypoinsulinemic/hyperglycemic with streptozotocin, and both AdipoR1 and AdipoR2 mRNA were almost completely restored by insulin treatment. These observations suggested that insulin may negatively regulate AdipoR1/R2 mRNA levels (81). The PI3-kinase inhibitor LY 294002 and constitutively active form of Foxo (Forkhead box, class O) 1 revealed that insulin repressed AdipoR1/R2 mRNA expressions via activation of PI3-kinase and inactivation of Foxo1 (81).
The expressions of both AdipoR1 and AdipoR2 were significantly decreased in muscle and adipose tissue of insulin-resistant ob/ob mice, which exhibited hyperglycemia and hyperinsulinemia, as compared with control mice (81) (Fig. 10). Scatchard plot analysis revealed that both high-affinity and low-affinity binding sites for globular adiponectin (gAd) and adiponectin binding in skeletal muscles of ob/ob mice were reduced as compared with those of wild-type mice, findings that are consistent with the fact that the numbers of both AdipoR1 and AdipoR2 were reduced. Moreover, adiponectin-induced activation of AMPK was impaired in skeletal muscle of ob/ob mice. These data suggest that adiponectin resistance was observed in ob/ob mice, which exhibited decreased expression levels of AdipoR1 and AdipoR2 (81) (Fig. 10).
We and others have previously shown that plasma adiponectin levels were decreased in obesity. This reduction may play a causal role in the development of insulin resistance. In the same study, we have also shown that obesity decreased the expression levels of AdipoR1/R2, thereby reducing adiponectin sensitivity, which finally leads to insulin resistance, the so-called "vicious cycle" (61) (Fig. 10).
A correlation has been reported between adiponectin receptor gene expression and insulin sensitivity in nondiabetic Mexican Americans with or without a family history of type 2 diabetes (82). Adiponectin receptor expression in skeletal muscle of type 2 diabetic patients was also reported to be decreased (83).
Our data suggest that not only agonism of AdipoR1/R2 but also strategies to increase AdipoR1/R2 may be a logical approach with which to provide a novel treatment modality for insulin resistance and type 2 diabetes.
IX. Adiponectin Hypothesis
Based upon the significant body of evidence discussed in this review, obtained from our and other laboratories, we propose the following adiponectin hypothesis (Fig. 11). Reduced adiponectin levels were caused by interactions of genetic factors such as SNPs in the adiponectin gene itself and environmental factors causing obesity such as a HF diet. Reduced adiponectin actions also resulted from down-regulation of adiponectin receptors linked to obesity. These reductions of adiponectin actions may play a crucial causal role in the development of insulin resistance, type 2 diabetes, metabolic syndrome, and atherosclerosis (Fig. 11).
X. Adiponectin and Adiponectin Receptors as Therapeutic Targets
According to our adiponectin hypothesis, a therapeutic strategy for type 2 diabetes, metabolic syndrome, and cardiovascular diseases may include the up-regulation of plasma adiponectin, up-regulation of adiponectin receptors, or the development of AdipoRs agonists.
A. Up-regulation of plasma adiponectin
Insulin sensitizer PPAR agonists have been shown to increase adiponectin levels in mice (31) and humans (84), as well as in 3T3L1 adipocytes in vitro (31). These effects seem to be associated with small-sized adipocytes (39), adipocytes differentiation (85, 86), direct transcriptional activation of genes via peroxisome proliferator response element (87, 88, 89, 90, 91), and increased insulin action (92). Interestingly, both PPAR agonists and adiponectin have been shown to increase insulin sensitivity and ameliorate atherosclerosis. To test whether the PPAR agonist-mediated improvement in insulin sensitivity and/or amelioration of atherosclerosis was dependent on adiponectin is very important, and thus it is very interesting to see the effects of PPAR agonists in adiponectin knockout mice.
B. Up-regulation of adiponectin receptors and development of AdipoRs agonists
The evidence described in this review indicates that reductions in plasma adiponectin levels and adiponectin receptors may play major roles in the development of insulin resistance, type 2 diabetes, metabolic syndrome, and cardiovascular diseases that are linked to obesity. With this in mind, one therapeutic strategy may be to up-regulate plasma adiponectin levels, which has already been discussed. The other strategy may be to up-regulate adiponectin receptors or to stimulate adiponectin receptors using small molecule agonists. We would like to introduce two interesting examples of attempts to develop such drugs.
Dr. Staels’ group reported that adiponectin receptors are expressed in human macrophages and that their expression levels may be regulated by agonists of the nuclear receptors PPAR, PPAR, and liver X receptor (93).
Osmotin is a pathogenesis-related (PR)-5 family of plant defense proteins that induces apoptosis in the yeast. Dr. Bressan’s group at Purdue University isolated and selected yeast clones that exhibited hypersensitivity to osmotin, sequenced their cDNA inserts, and found that PHO36/YOL002c, the yeast homolog of AdipoR, is a receptor for osmotin (94) (Fig. 12).
X-ray crystallographic studies revealed that both globular adiponectin and osmotin consist of antiparallel ?-strands arranged in the shape of a ?-barrel. The domain I (lectin-like domain) of osmotin can be overlapped with adiponectin, suggesting that the two proteins share the lectin-like domain (94) (Fig. 12).
Interestingly, osmotin could activate AMP kinase in C2C12 myocytes. More importantly, suppression of AdipoRs expression by siRNA markedly reduced phosphorylation of AMP kinase induced by osmotin. These data suggest that osmotin activates AMP kinase via AdipoRs in mammalian C2C12 myocytes (94).
Osmotin is a member of a large PR-5 protein family, which is both ubiquitous (fruits and vegetables, etc.) and diverse. PR-5 proteins are also extremely stable and may remain active even when in contact with the human digestive or respiratory systems. Osmotin, which is a ligand for the yeast homolog of AdipoR (PHO36), activates AMP kinase via AdipoR in C2C12 myocytes. These data raise the possibility that further research examining similarities in adiponectin and osmotin may facilitate the development of potential adiponectin receptor agonists (94).
C. Pleiotropic effects of adiponectin in relation to metabolic syndrome
In this review, we have stated that adiponectin increases insulin sensitivity in the liver and skeletal muscle and that adiponectin also reduces atherosclerosis. In addition to these effects, adiponectin also seems to have pleiotropic effects, particularly in relation to metabolic syndrome. Obesity has been reported to be associated with a higher incidence of certain cancers. Recently, adiponectin was reported to induce antiangiogenesis and antitumor activity via caspase-mediated endothelial cell apoptosis (95). Moreover, fatty liver and/or liver fibrosis are often associated with metabolic syndrome. Adiponectin was reported to alleviate alcoholic and nonalcoholic fatty liver diseases (96, 97) and liver fibrosis (98) in mice. Furthermore, it is possible that adiponectin stimulates insulin secretion and/or regulates energy homeostasis (99, 100). Further studies will be needed to determine the physiological and pathophysiological roles of AdipoR1 and AdipoR2 in these actions.
Acknowledgments
We thank Drs. R. Nagai, T. Shimizu, T. Yokomizo, K. Taira, M. Miyagishi, T. Kitamura, K. Tobe, K. Ueki, Y. Terauchi, K. Hara, N. Kubota, T. Sugiyama, J. Kamon, H. Waki, Y. Hada, S. Takekawa, A. Tsuchida, Y. Itoh, T. Maki, M. Kobayashi, K. Takasawa, S. Uchida, S. Kita, M. Noda, K. Eto, R. Suzuki, Y. Kaburagi, H. Kagechika, K. Shudo, (University of Tokyo), P. Froguel (Imperial College; UK), K. Komeda (Tokyo Medical University), Y. Akanuma and K. Kosaka (Institute for Diabetes Care and Research, Asahi Life Foundation), K. Murakami (Kyorin Pharmaceutical), Y. Oike (Keio University), and Y. Ueyama (Tokai University and Central Institute for Experimental Animals) for their helpful suggestions. We are grateful to A. Okano, A. Itoh, K. Miyata, S. Nakamura, Y. Mizuno, C. Katayama, and K. Nitta for their excellent technical assistance.
Footnotes
This work was supported by the Program for Promotion of Fundamental Studies in Health Sciences of the Organization for Pharmaceutical Safety and Research of Japan, a grant from the Human Science Foundation (to T.K.); a Grant-in-Aid for the Development of Innovative Technology from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to T.K.); a Grant-in Aid for Creative Scientific Research (10NP0201) from the Japan Society for the Promotion of Science (to T.K.); and Health Science Research Grants (Research on Human Genome and Gene Therapy) from the Ministry of Health, Labor and Welfare of Japan (to T.K.).
Abbreviations: ACC, Acetyl-coenzyme-A carboxylase; AMPK, AMP-activated protein kinase; apoE, apolipoprotein E; EGF, epidermal growth factor; gAd, globular adiponectin; HF, high-fat; HMW, high molecular weight; PI, phosphatidylinositol; PPAR, peroxisome proliferator-activated receptor; PR, pathogenesis-related; siRNA, small interfering RNA; SNP, single nucleotide polymorphism; TG, triglyceride.
References
Spiegelman BM, Flier JS 1996 Adipogenesis and obesity: rounding out the big picture. Cell 87:377–389
Reaven GM 1995 The fourth Musketeer—from Alexandre Dumas to Claude Bernard. Diabetologia 38:3–13
Shulman GI 2000 Cellular mechanisms of insulin resistance. J Clin Invest 106:171–176
White RT, Damm D, Hancock N, Rosen BS, Lowell BB, Usher P, Flier JS, Spiegelman BM 1992 Human adipsin is identical to complement factor D and is expressed at high levels in adipose tissue. J Biol Chem 267:9210–9213
Friedman JM 2000 Obesity in the new millennium. Nature 404:632–634
Shimomura I, Funahashi T, Takahashi M, Maeda K, Kotani K, Nakamura T, Yamashita S, Miura M, Fukuda Y, Takemura K, Tokunaga K, Matsuzawa Y 1996 Enhanced expression of PAI-1 in visceral fat: possible contributor to vascular disease in obesity. Nat Med 2:800–803
Steppan CM, Bailey ST, Bhat S, Brown EJ, Banerjee RR, Wright CM, Patel HR, Ahima RS, Lazar MA 2001 The hormone resistin links obesity to diabetes. Nature 409:307–312
Hotamisligil GS 1999 The role of TNF and TNF receptors in obesity and insulin resistance. J Intern Med 245:621–625
Beltowski J 2003 Adiponectin and resistin—new hormones of white adipose tissue. Med Sci Monit 9:RA55–RA61
Vasseur F, Lepretre F, Lacquemant C, Froguel P 2003 The genetics of adiponectin. Curr Diab Rep 3:151–158
Heilbronn LK, Smith SR, Ravussin E 2003 The insulin-sensitizing role of the fat derived hormone adiponectin. Curr Pharm Des 9:1411–1418
Wolf G 2003 Adiponectin: a regulator of energy homeostasis. Nutr Rev 61:290–292
Haluzik M, Parizkova J, Haluzik MM 2004 Adiponectin and its role in the obesity-induced insulin resistance and related complications. Physiol Res 53:123–129
Ukkola O, Santaniemi M 2002 Adiponectin: a link between excess adiposity and associated comorbidities? J Mol Med 80:696–702
Scherer PE, Williams S, Fogliano M, Baldini G, Lodish HF 1995 A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem 270:26746–26749
Hu E, Liang P, Spiegelman BM 1996 AdipoQ is a novel adipose-specific gene dysregulated in obesity. J Biol Chem 271:10697–10703
Maeda K, Okubo K., Shimomura I, Funahashi T, Matsuzawa Y, Matsubara K 1996 cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1). Biochem Biophys Res Commun 221:286–289
Nakano Y, Tobe T, Choi-Miura NH, Mazda T, Tomita M 1996 Isolation and characterization of GBP28, a novel gelatin-binding protein purified from human plasma. J Biochem (Tokyo) 120:803–812
Crouch E, Persson A, Chang D, Heuser J 1994 Molecular structure of pulmonary surfactant protein D (SP-D). J Biol Chem 269:17311–17319
McCormack FX, Pattanajitvilai S, Stewart J, Possmayer F, Inchley K, Voelker DR 1997 The Cys6 intermolecular disulfide bond and the collagen-like region of rat SP-A play critical roles in interactions with alveolar type II cells and surfactant lipids. J Biol Chem 272:27971–27979
Wong GW, Wang J, Hug C, Tsao TS, Lodish HF 2004 A family of Acrp30/adiponectin structural and functional paralogs. Proc Natl Acad Sci USA 101:10302–10307
Shapiro L, Scherer PE 1998 The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor. Curr Biol 8:335–340
Waki H, Yamauchi T, Kamon J, Ito Y, Uchida S, Kita S, Hara K, Hada Y, Vasseur F, Froguel P, Kimura S, Nagai R, Kadowaki T 2003 Impaired multimerization of human adiponectin mutants associated with diabetes: Molecular structure and multimer formation of adiponectin. J Biol Chem 278:40352–40363
Tsao T-S, Murrey HE, Hug C, Lee DH, Lodish HF 2002 Oligomerization state-dependent activation of NF-B signaling pathway by adipocyte complement-related protein of 30 kDa(Acrp30). J Biol Chem 277:29359–29362
Tsao TS, Tomas E, Murrey HE, Hug C, Lee DH, Ruderman NB, Heuser JE, Lodish HF 2003 Role of disulfide bonds in Acrp30/adiponectin structure and signaling specificity. Different oligomers activate different signal transduction pathways. J Biol Chem 278:50810–50817
Fruebis J, Tsao TS, Javorschi S, Ebbets-Reed D, Erickson MR, Yen FT, Bihain BE, Lodish HF 2001 Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice. Proc Natl Acad Sci USA 98:2005–2010
Waki H, Yamauchi T, Kamon J, Kita S, Ito Y, Hada Y, Uchida S, Tsuchida A, Takekawa S, Kadowaki T 2005 Generation of globular fragment of adiponectin by leukocyte elastase secreted by monocytic cell line THP-1. Endocrinology 146:790–796
Pajvani UB, Du X, Combs TP, Berg AH, Rajala MW, Schulthess T, Engel J, Brownlee M, Scherer PE 2003 Structure-function studies of the adipocyte-secreted hormone Acrp30/adiponectin. Implications for metabolic regulation and bioactivity. J Biol Chem 278:9073–9085
Wang Y, Xu A, Knight C, Xu LY, Cooper GJ 2002 Hydroxylation and glycosylation of the four conserved lysine residues in the collagenous domain of adiponectin. Potential role in the modulation of its insulin-sensitizing activity. J Biol Chem 277:19521–19529
Sato C, Yasukawa Z, Honda N, Matsuda T, Kitajima K 2001 Identification and adipocyte differentiation-dependent expression of the unique disialic acid residue in an adipose tissue-specific glycoprotein, adipo Q. J Biol Chem 276:28849–28856
Yamauchi T, Kamon J, Waki H, Terauchi Y, Kubota N, Hara K, Mori Y, Ide T, Murakami K, Tsuboyama-Kasaoka N, Ezaki O, Akanuma Y, Gavrilova O, Vinson C, Reitman ML, Kagechika H, Shudo K, Yoda M, Nakano Y, Tobe K, Nagai R, Kimura S, Tomita M, Froguel P, Kadowaki T 2001 The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med 7:941–946
Arita Y, Kihara S, Ouchi N, Takahashi M, Maeda K, Miyagawa J, Hotta K, Shimomura I, Nakamura T, Miyaoka K, Kuriyama H, Nishida M, Yamashita S, Okubo K, Matsubara K, Muraguchi M, Ohmoto Y, Funahashi T, Matsuzawa Y 1999 Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity. Biochem Biophys Res Commun 257:79–83
Hotta K, Funahashi T, Arita Y, Takahashi M, Matsuda M, Okamoto Y, Iwahashi H, Kuriyama H, Ouchi N, Maeda K, Nishida M, Kihara S, Sakai N, Nakajima T, Hasegawa K, Muraguchi M, Ohmoto Y, Nakamura T, Yamashita S, Hanafusa T, Matsuzawa Y 2000 Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients. Arterioscler Thromb Vasc Biol 20:1595–1599
Kumada M, Kihara S, Sumitsuji S, Kawamoto T, Matsumoto S, Ouchi N, Arita Y, Okamoto Y, Shimomura I, Hiraoka H, Nakamura T, Funahashi T, Matsuzawa Y; Osaka CAD Study Group 2003 Association of hypoadiponectinemia with coronary artery disease in men. Arterioscler Thromb Vasc Biol 23:85–89
Ouchi N, Ohishi M, Kihara S, Funahashi T, Nakamura T, Nagaretani H, Kumada M, Ohashi K, Okamoto Y, Nishizawa H, Kishida K, Maeda N, Nagasawa A, Kobayashi H, Hiraoka H, Komai N, Kaibe M, Rakugi H, Ogihara T, Matsuzawa Y 2003 Association of hypoadiponectinemia with impaired vasoreactivity. Hypertension 42:231–234
Trujillo ME, Scherer PE 2005 Adiponectin: journey from an adipocyte secretory protein to biomarker of the metabolic syndrome. J Intern Med 257:167–175
Berg AH, Combs TP, Du X, Brownlee M, Scherer PE 2001 The adipocyte-secreted protein Acrp30 enhances hepatic insulin action. Nat Med 7:947–953
Kubota N, Terauchi Y, Miki H, Tamemoto H, Yamauchi T, Komeda K, Satoh S, Nakano R, Ishii C, Sugiyama T, Eto K, Tsubamoto Y, Okuno A, Murakami K, Sekihara H, Hasegawa G, Naito M, Toyoshima Y, Tanaka S, Shiota K, Kitamura T, Fujita T, Ezaki O, Aizawa S, Nagai R, Tobe K, Kimura S, Kadowaki T 1999 PPAR mediates high-fat diet-induced adipocyte hypertrophy and insulin resistance. Mol Cell 4:597–609
Yamauchi T, Kamon J, Waki H, Murakami K, Motojima K, Komeda K, Ide T, Kubota N, Terauchi Y, Tobe K, Miki H, Tsuchida A, Akanuma Y, Nagai R, Kimura S, Kadowaki T 2001 The mechanisms by which both heterozygous PPAR deficiency and PPAR agonist improve insulin resistance. J Biol Chem 276:41245–41254
Shimomura I, Hammer RE, Ikemoto S, Brown MS, Goldstein JL 1999 Leptin reverses insulin resistance and diabetes mellitus in mice with congenital lipodystrophy. Nature 401:73–76
Yamauchi T, Waki H, Kamon J, Murakami K, Motojima K, Komeda K, Miki H, Kubota N, Terauchi Y, Tsuchida A, Tsuboyama-Kasaoka N, Yamauchi N, Ide T, Hori W, Kato S, Fukayama M, Akanuma Y, Ezaki O, Itai A, Nagai R, Kimura S, Tobe K, Kagechika H, Shudo K, Kadowaki T 2001 Inhibition of RXR and PPAR ameliorates diet-induced obesity and type 2 diabetes. J Clin Invest 108:1001–1013
Combs TP, Berg AH, Obici S, Scherer PE, Rossetti L 2001 Endogenous glucose production is inhibited by the adipose-derived protein Acrp30. J Clin Invest 108:1875–1881
Yamauchi T, Kamon J, Waki H, Imai Y, Shimozawa N, Hioki K, Uchida S, Ito Y, Takakuwa K, Matsui J, Takata M, Eto K, Terauchi Y, Komeda K, Tsunoda M, Murakami K, Ohnishi Y, Naitoh T, Yamamura K, Ueyama Y, Froguel P, Kimura S, Nagai R, Kadowaki T 2003 Globular adiponectin protected ob/ob mice from diabetes and apoE-deficient mice from atherosclerosis. J Biol Chem 278:2461–2468
Combs TP, Pajvani UB, Berg AH, Lin Y, Jelicks LA, Laplante M, Nawrocki AR, Rajala MW, Parlow AF, Cheeseboro L, Ding YY, Russell RG, Lindemann D, Hartley A, Baker GR, Obici S, Deshaies Y, Ludgate M, Rossetti L, Scherer PE 2004 A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivity. Endocrinology 145:367–383
Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, Eto K, Yamashita T, Kamon J, Satoh H, Yano W, Nagai R, Kimura S, Kadowaki T, Noda T 2002 Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem 277:25863–25866
Maeda N, Shimomura I, Kishida K, Nishizawa H, Matsuda M, Nagaretani H, Furuyama N, Kondo H, Takahashi M, Arita Y, Komuro R, Ouchi N, Kihara S, Tochino Y, Okutomi K, Horie M, Takeda S, Aoyama T, Funahashi T, Matsuzawa Y 2002 Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med 8:731–737
Ma K, Cabrero A, Saha PK, Kojima H, Li L, Chang BH, Paul A, Chan L 2002 Increased ?-oxidation but no insulin resistance or glucose intolerance in mice lacking adiponectin. J Biol Chem 277:34658–34661
Shklyaev S, Aslanidi G, Tennant M, Prima V, Kohlbrenner E, Kroutov V, Campbell-Thompson M, Crawford J, Shek EW, Scarpace PJ, Zolotukhin S 2003 Sustained peripheral expression of transgene adiponectin offsets the development of diet-induced obesity in rats. Proc Natl Acad Sci USA 100:14217–14222
Okamoto Y, Kihara S, Ouchi N, Nishida M, Arita Y, Kumada M, Ohashi K, Sakai N, Shimomura I, Kobayashi H, Terasaka N, Inaba T, Funahashi T, Matsuzawa Y 2002 Adiponectin reduces atherosclerosis in apolipoprotein E-deficient mice. Circulation 106:2767–2770
Matsuda M, Shimomura I, Sata M, Arita Y, Nishida M, Maeda N, Kumada M, Okamoto Y, Nagaretani H, Nishizawa H, Kishida K, Komuro R, Ouchi N, Kihara S, Nagai R, Funahashi T, Matsuzawa Y 2002 Role of adiponectin in preventing vascular stenosis. The missing link of adipo-vascular axis. J Biol Chem 277:37487–37491
Yamauchi T, Kamon J, Minokoshi Y, Ito Y, Waki H, Uchida S, Yamashita S, Noda M, Kita S, Ueki K, Eto K, Akanuma Y, Froguel P, Foufelle F, Ferre P, Carling D, Kimura S, Nagai R, Kahn BB, Kadowaki T 2002 Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase. Nat Med 8:1288–1295
Tomas E, Tsao TS, Saha AK, Murrey HE, Zhang Cc C, Itani SI, Lodish HF, Ruderman NB 2002 Enhanced muscle fat oxidation and glucose transport by ACRP30 globular domain: acetyl-CoA carboxylase inhibition and AMP-activated protein kinase activation. Proc Natl Acad Sci USA 99:16309–16313
Wu X, Motoshima H, Mahadev K, Stalker TJ, Scalia R, Goldstein BJ 2003 Involvement of AMP-activated protein kinase in glucose uptake stimulated by the globular domain of adiponectin in primary rat adipocytes. Diabetes 52:1355–1363
Minokoshi Y, Kim YB, Peroni OD, Fryer LG, Muller C, Carling D, Kahn BB 2002 Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase. Nature 415:339–343
Pajvani UB, Hawkins M, Combs TP, Rajala MW, Doebber T, Berger JP, Wagner JA, Wu M, Knopps A, Xiang AH, Utzschneider KM, Kahn SE, Olefsky JM, Buchanan TA, Scherer PE 2004 Complex distribution, not absolute amount of adiponectin, correlates with thiazolidinedione-mediated improvement in insulin sensitivity. J Biol Chem 279:12152–12162
Nishizawa H, Shimomura I, Kishida K, Maeda N, Kuriyama H, Nagaretani H, Matsuda M, Kondo H, Furuyama N, Kihara S, Nakamura T, Tochino Y, Funahashi T, Matsuzawa Y 2002 Androgens decrease plasma adiponectin, an insulin-sensitizing adipocyte-derived protein. Diabetes 51:2734–2741
Combs TP, Berg AH, Rajala MW, Klebanov S, Iyengar P, Jimenez-Chillaron JC, Patti ME, Klein SL, Weinstein RS, Scherer PE 2003 Sexual differentiation, pregnancy, calorie restriction, and aging affect the adipocyte-specific secretory protein adiponectin. Diabetes 52:268–276
Matsuzawa Y, Shimomura I, Kihara S, Funahashi T 2003 Importance of adipocytokines in obesity-related diseases. Horm Res 60(Suppl 3):56–59
Matsuzawa Y, Funahashi T, Kihara S, Shimomura I 2004 Adiponectin and metabolic syndrome. Arterioscler Thromb Vasc Biol 24:29–33
Funahashi T, Nakamura T, Shimomura I, Maeda K, Kuriyama H, Takahashi M, Arita Y, Kihara S, Matsuzawa Y 1999 Role of adipocytokines on the pathogenesis of atherosclerosis in visceral obesity. Intern Med 38:202–206
Ouchi N, Kihara S, Arita Y, Okamoto Y, Maeda K, Kuriyama H, Hotta K, Nishida M, Takahashi M, Muraguchi M, Ohmoto Y, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 2000 Adiponectin, an adipocyte-derived plasma protein, inhibits endothelial NF-B signaling through a cAMP-dependent pathway. Circulation 102:1296–1301
Ouchi N, Kihara S, Arita Y, Maeda K, Kuriyama H, Okamoto Y, Hotta K, Nishida M, Takahashi M, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 1999 Novel modulator for endothelial adhesion molecules: adipocyte-derived plasma protein adiponectin. Circulation 100:2473–2476
Ouchi N, Kihara S, Arita Y, Nishida M, Matsuyama A, Okamoto Y, Ishigami M, Kuriyama H, Kishida K, Nishizawa H, Hotta K, Muraguchi M, Ohmoto Y, Yamashita S, Funahashi T, Matsuzawa Y 2001 Adipocyte-derived plasma protein, adiponectin, suppresses lipid accumulation and class A scavenger receptor expression in human monocyte-derived macrophages. Circulation 103:1057–1063
Arita Y, Kihara S, Ouchi N, Maeda K, Kuriyama H, Okamoto Y, Kumada M, Hotta K, Nishida M, Takahashi M, Nakamura T, Shimomura I, Muraguchi M, Ohmoto Y, Funahashi T, Matsuzawa Y 2002 Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB-binding protein and regulates growth factor-induced common postreceptor signal in vascular smooth muscle cell. Circulation 105:2893–2898
Kobayashi H, Ouchi N, Kihara S, Walsh K, Kumada M, Abe Y, Funahashi T, Matsuzawa Y 2004 Selective suppression of endothelial cell apoptosis by the high molecular weight form of adiponectin. Circ Res 94:e27–e31
Chen H, Montagnani M, Funahashi T, Shimomura I, Quon MJ 2003 Adiponectin stimulates production of nitric oxide in vascular endothelial cells. J Biol Chem 278:45021–45026
Kumada M, Kihara S, Ouchi N, Kobayashi H, Okamoto Y, Ohashi K, Maeda K, Nagaretani H, Kishida K, Maeda N, Nagasawa A, Funahashi T, Matsuzawa Y 2004 Adiponectin specifically increased tissue inhibitor of metalloproteinase-1 through interleukin-10 expression in human macrophages. Circulation 109:2046–2049
Mori Y, Otabe S, Dina C, Yasuda K, Populaire C, Lecoeur C, Vatin V, Durand E, Hara K, Okada T, Tobe K, Boutin P, Kadowaki T, Froguel P 2002 Genome-wide search for type 2 diabetes in japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p. Diabetes 51:1247–1255
Hara K, Boutin P, Mori Y, Tobe K, Dina C, Yasuda K, Yamauchi T, Otabe S, Okada T, Eto K, Kadowaki H, Hagura R, Akanuma Y, Yazaki Y, Nagai R, Taniyama M, Matsubara K, Yoda M, Nakano Y, Tomita M, Kimura S, Ito C, Froguel P, Kadowaki T 2002 Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the japanese population. Diabetes 51:536–540
Vasseur F, Helbecque N, Dina C, Lobbens S, Delannoy V, Gaget S, Boutin P, Vaxillaire M, Lepretre F, Dupont S, Hara K, Clement K, Bihain B, Kadowaki T, Froguel P 2002 Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians. Hum Mol Genet 11:2607–2614
Stumvoll M, Tschritter O, Fritsche A, Staiger H, Renn W, Weisser M, Machicao F, Haring H 2002 Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity: interaction with family history of type 2 diabetes. Diabetes 51:37–41
Menzaghi C, Ercolino T, Paola RD, Berg AH, Waaram JH, Scherer PE, Trischitta V, Doria A 2002 A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome. Diabetes 51:2306–2312
Lindsay RS, Funahashi T, Hanson RL, Matsuzawa Y, Tanaka S, Tataranni PA, Knowler WC, Krakoff J 2002 Adiponectin and development of type 2 diabetes in the Pima Indian population. Lancet 360:57–58
Takahashi M, Arita Y, Yamagata K, Matsukawa Y, Okutomi K, Horie M, Shimomura I, Hotta K, Kuriyama H, Kihara S, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 2000 Genomic structure and mutations in adipose-specific gene, adiponectin. Int J Obes Relat Metab Disord 24:861–868
Kondo H, Shimomura I, Matsukawa Y, Kumada M, Takahashi M, Matsuda M, Ouchi N, Kihara S, Kawamoto T, Sumitsuji S, Funahashi T, Matsuzawa Y 2002 Association of adiponectin mutation with type 2 diabetes: a candidate gene for the insulin resistance syndrome. Diabetes 51:2325–2328
Yamauchi T, Kamon J, Ito Y, Tsuchida A, Yokomizo T, Kita S, Sugiyama T, Miyagishi M, Hara, K, Tsunoda M, Murakami K, Ohteki T, Uchida S, Takekawa S, Waki H, Tsuno NH, Shibata Y, Terauchi Y, Froguel P, Tobe K, Koyasu S, Taira K, Kitamura T, Shimizu T, Nagai R, Kadowaki T 2003 Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature [Erratum (2004) 431:1123] 423:762–769
Karpichev IV, Cornivelli L, Small GM 2002 Multiple regulatory roles of a novel Saccharomyces cerevisiae protein, encoded by YOL002c, in lipid and phosphate metabolism. J Biol Chem 277:12152–12162
Kharroubi I, Rasschaert J, Eizirik DL, Cnop M 2003 Expression of adiponectin receptors in pancreatic ? cells. Biochem Biophys Res Commun 312:1118–1122
Fasshauer M, Klein J, Kralisch S, Klier M, Lossner U, Bluher M, Paschke R 2004 Growth hormone is a positive regulator of adiponectin receptor 2 in 3T3–L1 adipocytes. FEBS Lett 558:27–32
Hug C, Wang J, Ahmad NS, Bogan JS, Tsao TS, Lodish HF 2004 T-cadherin is a receptor for hexameric and high-molecular-weight forms of Acrp30/adiponectin. Proc Natl Acad Sci USA 101:10308–10313
Tsuchida A, Yamauchi T, Ito Y, Hada Y, Maki T, Takekawa S, Kamon J, Kobayashi M, Suzuki R, Hara K, Kubota N, Terauchi Y, Froguel P, Nakae J, Kasuga M, Accili D, Tobe K, Ueki K, Nagai R, Kadowaki T 2004 Insulin/Foxo1 pathway regulates expression levels of adiponectin receptors and adiponectin sensitivity. J Biol Chem 279:30817–30822
Civitarese AE, Jenkinson CP, Richardson D, Bajaj M, Cusi K, Kashyap S, Berria R, Belfort R, DeFronzo RA, Mandarino LJ, Ravussin E 2004 Adiponectin receptors gene expression and insulin sensitivity in non-diabetic Mexican Americans with or without a family history of type 2 diabetes. Diabetologia 47:816–820
Debard C, Laville M, Berbe V, Loizon E, Guillet C, Morio-Liondore B, Boirie Y, Vidal H 2004 Expression of key genes of fatty acid oxidation, including adiponectin receptors, in skeletal muscle of type 2 diabetic patients. Diabetologia 47:917–925
Hirose H, Kawai T, Yamamoto Y, Taniyama M, Tomita M, Matsubara K, Okazaki Y, Ishii T, Oguma Y, Takei I, Saruta T 2002 Effects of pioglitazone on metabolic parameters, body fat distribution, and serum adiponectin levels in Japanese male patients with type 2 diabetes. Metabolism 51:314–317
Das K, Lin Y, Widen E, Zhang Y, Scherer PE 2001 Chromosomal localization, expression pattern, and promoter analysis of the mouse gene encoding adipocyte-specific secretory protein Acrp30. Biochem Biophys Res Commun 280:1120–1129
Saito K, Tobe T, Yoda M, Nakano Y, Choi-Miura NH, Tomita M 1999 Regulation of gelatin-binding protein 28 (GBP28) gene expression by C/EBP. Biol Pharm Bull 22:1158–1162
Iwaki M, Matsuda M, Maeda N, Funahashi T, Matsuzawa Y, Makishima M, Shimomura I 2003 Induction of adiponectin, a fat-derived antidiabetic and antiatherogenic factor, by nuclear receptors. Diabetes 52:1655–1663
Maeda N, Takahashi M, Funahashi T, Kihara S, Nishizawa H, Kishida K, Nagaretani H, Matsuda M, Komuro R, Ouchi N, Kuriyama H, Hotta K, Nakamura T, Shimomura I, Matsuzawa Y 2001 PPAR ligands increase expression and plasma concentrations of adiponectin, an adipose-derived protein. Diabetes 50:2094–2099
Bouskila M, Pajvani UB, Scherer PE 2005 Adiponectin: a relevant player in PPAR-agonist-mediated improvements in hepatic insulin sensitivity? Int J Obes Relat Metab Disord 29(Suppl 1):S17–23
Tonelli J, Li W, Kishore P, Pajvani UB, Kwon E, Weaver C, Scherer PE, Hawkins M 2004 Mechanisms of early insulin-sensitizing effects of thiazolidinediones in type 2 diabetes. Diabetes 53:1621–1629
Combs TP, Wagner JA, Berger J, Doebber T, Wang WJ, Zhang BB, Tanen M, Berg AH, O’Rahilly S, Savage DB, Chatterjee K, Weiss S, Larson PJ, Gottesdiener KM, Gertz BJ, Charron MJ, Scherer PE, Moller DE 2002 Induction of adipocyte complement-related protein of 30 kilodaltons by PPAR agonists: a potential mechanism of insulin sensitization. Endocrinology 143:998–1007
Terauchi Y, Matsui J, Kamon J, Yamauchi T, Kubota N, Komeda K, Aizawa S, Akanuma Y, Tomita M, Kadowaki T 2004 Increased serum leptin protects from adiposity despite the increased glucose uptake in white adipose tissue in mice lacking p85 phosphoinositide 3-kinase. Diabetes 53:2261–2270
Chinetti G, Zawadski C, Fruchart JC, Staels B 2004 Expression of adiponectin receptors in human macrophages and regulation by agonists of the nuclear receptors PPAR, PPAR, and LXR. Biochem Biophys Res Commun 314:151–158
Narasimhan LM, Coca MA, Jin J, Yamauchi T, Ito Y, Kadowaki T, Kim KK, Pardo JM, Damsz B, Bressan RA, Yun DJ 2005 Osmotin is a homolog of mammalian adiponectin and controls apoptosis in yeast through a homolog of mammalian adiponectin receptor. Mol Cell 17:171–180
Brakenhielm E, Veitonmaki N, Cao R, Kihara S, Matsuzawa Y, Zhivotovsky B, Funahashi T, Cao Y 2004 Adiponectin-induced antiangiogenesis and antitumor activity involve caspase-mediated endothelial cell apoptosis. Proc Natl Acad Sci USA 101:2476–2481
Xu A, Wang Y, Keshaw H, Xu LY, Lam KS, Cooper GJ 2003 The fat-derived hormone adiponectin alleviates alcoholic and nonalcoholic fatty liver diseases in mice. J Clin Invest 112:91–100
Yoda-Murakami M, Taniguchi M, Takahashi K, Kawamata S, Saito K, Choi-Miura NH, Tomita M 2001 Change in expression of GBP28/adiponectin in carbon tetrachloride-administrated mouse liver. Biochem Biophys Res Commun 285:372–377
Kamada Y, Tamura S, Kiso S, Matsumoto H, Saji Y, Yoshida Y, Fukui K, Maeda N, Nishizawa H, Nagaretani H, Okamoto Y, Kihara S, Miyagawa J, Shinomura Y, Funahashi T, Matsuzawa Y 2003 Enhanced carbon tetrachloride-induced liver fibrosis in mice lacking adiponectin. Gastroenterology 125:1796–1807
Masaki T, Chiba S, Yasuda T, Tsubone T, Kakuma T, Shimomura I, Funahashi T, Matsuzawa Y, Yoshimatsu H 2003 Peripheral, but not central, administration of adiponectin reduces visceral adiposity and upregulates the expression of uncoupling protein in agouti yellow (Ay/a) obese mice. Diabetes 52:2266–2273
Qi Y, Takahashi N, Hileman SM, Patel HR, Berg AH, Pajvani UB, Scherer PE, Ahima RS 2004 Adiponectin acts in the brain to decrease body weight. Nat Med 10:524–529
Yamauchi T, Hara K, Kubota N, Terauchi Y, Tobe K, Froguel P, Nagai R, Kadowaki T 2003 Dual roles of adiponectin/Acrp30 in vivo as an anti-diabetic and anti-atherogenic adipokine. Curr Drug Targets Immune Endocr Metabol Disord 3:243–254(Takashi Kadowaki and Tosh)
Department of Integrated Molecular Science on Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan
Core Research for Evolutional Science and Technology of Japan Science and Technology Agency, Kawaguchi 332-0012, Japan
Abstract
Metabolic syndrome is thought to result from obesity and obesity-linked insulin resistance. Obesity in adulthood is characterized by adipocyte hypertrophy. Adipose tissue participates in the regulation of energy homeostasis as an important endocrine organ that secretes a number of biologically active "adipokines."
Heterozygous peroxisome proliferator-activated receptor- knockout mice were protected from high-fat diet induced obesity, adipocyte hypertrophy, and insulin resistance. Systematic gene profiling analysis of these mice revealed that adiponectin/Acrp30 was overexpressed. Functional analyses including generation of adiponectin transgenic or knockout mice have revealed that adiponectin serves as an insulin-sensitizing adipokine. In fact, obesity-linked down-regulation of adiponectin was a mechanism whereby obesity could cause insulin resistance and diabetes.
Recently, we have cloned adiponectin receptors in the skeletal muscle (AdipoR1) and liver (AdipoR2), which appear to comprise a novel cell-surface receptor family. We showed that AdipoR1 and AdipoR2 serve as receptors for globular and full-length adiponectin and mediate increased AMP-activated protein kinase, peroxisome proliferator-activated receptor- ligand activities, and glucose uptake and fatty-acid oxidation by adiponectin. Obesity decreased expression levels of AdipoR1/R2, thereby reducing adiponectin sensitivity, which finally leads to insulin resistance, the so-called "vicious cycle." Most recently, we showed that osmotin, which is a ligand for the yeast homolog of AdipoR (PHO36), activated AMPK via AdipoR in C2C12 myocytes. This may facilitate efficient development of adiponectin receptor agonists.
Adiponectin receptor agonists and adiponectin sensitizers should serve as versatile treatment strategies for obesity-linked diseases such as diabetes and metabolic syndrome.
I. Introduction
II. Identification and Molecular Structure
A. Identification
B. Molecular structure and multimeric form of adiponectin
III. Adiponectin and Insulin Resistance
A. Low plasma adiponectin levels and insulin resistance
B. Insulin-sensitizing effects of adiponectin
IV. Mouse Models
V. Mechanism of Action of Adiponectin
A. Insulin-sensitizing actions
B. Antiatherosclerotic actions
VI. Alterations in Adiponectin Gene Are Associated with Human Diabetes
VII. Cloning of Adiponectin Receptors AdipoR1 and AdipoR2
VIII. Regulation of Adiponectin Receptors
A. Regulation of expression levels of AdipoR1 and AdipoR2
IX. Adiponectin Hypothesis
X. Adiponectin and Adiponectin Receptors as Therapeutic Targets
A. Up-regulation of plasma adiponectin
B. Up-regulation of adiponectin receptors and development of AdipoRs agonists
C. Pleiotropic effects of adiponectin in relation to metabolic syndrome
I. Introduction
HIGH-FAT (HF) diet-induced insulin resistance associated with obesity is a major risk factor for diabetes and cardiovascular diseases, the prevalence of which is increasing sharply (1, 2). However, the molecular basis for this association remains to be elucidated. The adipose tissue itself serves as the site of triglyceride (TG) storage and free fatty acid/glycerol release in response to changing energy demands (1). Adipose tissue also participates in the regulation of energy homeostasis as an important endocrine organ that secretes a number of biologically active adipokines such as free fatty acid (3), adipsin (4), leptin (5), plasminogen activator inhibitor-1 (6), resistin (7), and TNF- (8). Adiponectin is one such adipokine that has recently attracted much attention. In this review, we will describe recent progress made in adiponectin research with particular emphasis on the role of adiponectin in the regulation of insulin sensitivity and the development of insulin resistance. Other aspects of adiponectin research have been reviewed elsewhere (9, 10, 11, 12, 13, 14).
II. Identification and Molecular Structure
A. Identification
Adiponectin was originally identified independently by four groups using different approaches. Mouse cDNAs for adiponectin, termed Acrp30 (15) and AdipoQ (16), were cloned by differential display before and after differentiation of mouse 3T3-L1 and 3T3-F442A cells. Human adiponectin cDNA was isolated by large-scale random sequencing of a 3'-directed human adipose tissue cDNA library (17). Human adiponectin was also purified from plasma as a gelatin binding protein, GBP28 (18).
B. Molecular structure and multimeric form of adiponectin
Adiponectin structurally belongs to the complement 1q family (19, 20, 21) (Fig. 1) and is known to form a characteristic homomultimer (22) (Fig. 2). It has been demonstrated that simple SDS-PAGE under nonreducing and non-heat-denaturing conditions clearly separates multimeric species of adiponectin (23) (Fig. 2). Adiponectin in human or mouse serum and adiponectin expressed in NIH-3T3 cells or Escherichia coli forms a wide range of multimers from trimers and hexamers to high molecular weight (HMW) multimers (23) such as dodecamers and 18 mers, as demonstrated by ourselves and other groups (22, 24, 25) (Fig. 2).
Adiponectin can exist as full-length or a smaller, globular fragment; however, almost all adiponectin appears to exist as full-length adiponectin in plasma. Lodish’s group reported that a small amount of globular adiponectin was detected in human plasma (26) (Fig. 1). It has been proposed that the globular fragment is generated by proteolytic cleavage, and recently it has been shown that the cleavage of adiponectin by leukocyte elastase secreted from activated monocytes and/or neutrophils could be responsible for the generation of the globular fragment of adiponectin (27). However, the pathophysiological importance of adiponectin cleavage by leukocyte elastase in vivo remains to be determined.
Oligomer formation of adiponectin depends on disulfide bond formation mediated by Cys-39 (28). Interestingly, a mutant adiponectin with a substitution of Cys by Ser at codon 39, which formed a trimer and readily underwent proteolytic cleavage, showed much more potent bioactivity, such as reduction of glucose output from primary hepatocytes, than wild-type adiponectin with a HMW.
Hydroxylation and glycosylation of the four lysines in the collagenous domain of adiponectin have been shown to play important roles in enhancing the ability of subphysiological concentrations of insulin to inhibit gluconeogenesis in hepatocytes (29). Adiponectin was reported to be an 2,8-linked disialic acid-containing glycoprotein, although the biological functions of the disialic acid epitope of adiponectin remain to be elucidated (30).
III. Adiponectin and Insulin Resistance
A. Low plasma adiponectin levels and insulin resistance
Spiegelman’s group reported that adiponectin expression is exclusive to adipose tissue and that the mRNA expression of adiponectin was reduced in obese diabetic murine model db/db mice (16). Plasma levels of adiponectin have also been reported to be significantly reduced in obese/diabetic mice and humans (16, 31, 32). Moreover, plasma adiponectin levels have been shown to be decreased in patients with cardiovascular diseases (33, 34), hypertension (35), or metabolic syndrome (36). Thus, reductions in plasma adiponectin levels are commonly observed in a variety of states frequently associated with insulin resistance. However, whether this apparent parallelism between low plasma adiponectin levels and insulin resistance represents a cause and effect relationship was not known.
B. Insulin-sensitizing effects of adiponectin
The insulin-sensitizing effect of adiponectin was first identified by three independent groups in 2001 (26, 31, 37). We previously generated heterozygous PPAR (peroxisome proliferator-activated receptor) knockout mice that remained insulin-sensitive on a HF diet (38). In an attempt to identify insulin-sensitizing molecules secreted from white adipose tissue of heterozygous PPAR knockout mice, oligonucleotide microarray analysis was carried out using white adipose tissue (39). Adiponectin as well as leptin expression was up-regulated. Leptin was previously shown to be a major insulin-sensitizing adipokine (40).
To verify the direct insulin-sensitizing effect of adiponectin in vivo, an insulin-resistant lipoatrophic diabetic mouse model that displays both adiponectin and leptin deficiency was employed (41). Replenishment of a physiological dose of recombinant adiponectin to the lipoatrophic diabetic mice significantly ameliorated insulin resistance (31). Moreover, insulin resistance in lipoatrophic mice was completely reversed by the combination of physiological doses of adiponectin and leptin, but only partially by either adiponectin or leptin alone (31). These data clearly indicate that adiponectin has a direct insulin-sensitizing action. These data also suggest that leptin and adiponectin may be the two major insulin-sensitizing hormones secreted from adipose tissue.
We also studied whether adiponectin can improve insulin resistance and diabetes in murine models of type 2 diabetes, characterized by obesity, insulin resistance, and hyperglycemia. Serum adiponectin levels were decreased in KKAy mice on a HF diet compared with those under a high-carbohydrate diet (31) (Fig. 3). Lower serum adiponectin levels in KKAy mice on the HF diet were partially restored by replenishment of recombinant adiponectin. Importantly, replenishment of adiponectin significantly ameliorated HF diet-induced insulin resistance and hypertriglyceridemia (31) (Fig. 3). These data suggest that the insulin resistance associated with HF diets and obesity is caused at least in part by the decreases in adiponectin linked to those circumstances. The data suggest that the fat-derived hormone adiponectin is decreased in obesity and deficient in lipoatrophy, and that reduction in adiponectin plays causal roles in the development of insulin resistance in these models.
Scherer’s group has reported that an acute increase in circulating adiponectin levels triggers a transient decrease in basal glucose levels by inhibiting both the expression of hepatic gluconeogenic enzymes and the rate of endogenous glucose production in both wild-type mice and a type 2 diabetes mouse model (37, 42), consistent with the proposal that adiponectin sensitizes the body to insulin. Lodish’s group reported that a proteolytic cleavage product of adiponectin increases fatty-acid oxidation in muscle and causes a decrease in plasma glucose and weight loss in mice (26).
These data raise the possibility that the replenishment of adiponectin may provide a novel treatment modality for insulin resistance and type 2 diabetes.
IV. Mouse Models
The chronic effects of adiponectin on insulin resistance in vivo were investigated by generating globular adiponectin transgenic mice (43, 44) or adiponectin-deficient mice (45, 46, 47). Globular adiponectin transgenic mice were generated and crossed with ob/ob mice (45). Globular adiponectin transgenic ob/ob mice showed partial amelioration of insulin resistance and diabetes, but not of obesity (43). These data suggested that chronic elevation of globular adiponectin has a direct insulin-sensitizing effect independent of white adipose tissue mass.
Scherer’s group reported that transgenic mice with a deletion in the collagenous domain of adiponectin displayed 3-fold elevated levels of circulating adiponectin, raised lipid clearance and lipoprotein lipase activity, and improved insulin-mediated suppression of endogenous glucose production, thereby improving insulin sensitivity (44). In rats, sustained peripheral expression of adiponectin by the transgene also offset the development of diet-induced obesity (48).
Globular adiponectin transgenic mice were also crossed with apolipoprotein E (apoE)-deficient mice to study whether globular adiponectin can inhibit atherosclerosis in vivo (43). apoE-Deficient mice are hypercholesterolemic and spontaneously develop severe atherosclerosis. We compared the extent of atherosclerotic lesions of globular adiponectin transgenic apoE-deficient mice to that in control apoE-deficient mice. Although serum parameters such as total cholesterol, TG, glucose, and insulin were not altered, the en face Sudan IV-positive lesion areas of the arch and the descending aorta were significantly smaller in globular adiponectin transgenic apoE-deficient mice than in control apoE-deficient littermates (43). Similar results were obtained by using adenoviral-mediated overexpression of adiponectin in apoE knockout mice (49). Thus, overexpression of adiponectin resulted in marked reduction of atherosclerotic lesion formation. Together with the observations that adiponectin can ameliorate diabetes and hyperlipidemia, adiponectin can reduce atherosclerosis both via direct effects on vascular wall and via reduction in risk factors.
To determine the physiological role of adiponectin, we and others have generated adiponectin knockout mice and reported that adiponectin-deficient mice exhibited characteristics of the metabolic syndrome such as insulin resistance, glucose intolerance, hyperlipidemia, and hypertension (35, 45, 46).
We and others also studied the role of adiponectin in vascular wall using adiponectin knockout mice (45, 50). We placed a cuff around the femoral artery to induce inflammation of the adventitia and subsequent neointimal formation 2 wk after cuff placement. Intimal thickness was significantly greater (2-fold) in adiponectin knockout mice than in the wild-type mice. Thus, adiponectin plays a protective role against neointimal formation in response to injury (45, 50).
V. Mechanism of Action of Adiponectin
A. Insulin-sensitizing actions
1. Adiponectin reduces tissue TG content and up-regulates insulin signaling.
Interestingly, in skeletal muscle, adiponectin increased expression of molecules involved in fatty-acid transport such as CD36, in combustion of fatty-acid such as acyl-coenzyme A oxidase, and in energy dissipation such as uncoupling protein 2. These changes led to decreased tissue TG content in skeletal muscle (31).
Increased tissue TG content has been reported to interfere with insulin-stimulated phosphatidylinositol (PI) 3-kinase activation and subsequent glucose transporter 4 translocation and glucose uptake, leading to insulin resistance (3). Thus, decreased tissue TG content in muscle may contribute to improved insulin signal transduction. This was demonstrated in skeletal muscle of lipoatrophic mice treated with adiponectin, in which increases in insulin-induced tyrosine phosphorylation of insulin receptor and insulin receptor substrate-1 and insulin-stimulated phosphorylation of Akt were seen (31).
2. Adiponectin activates PPAR.
Based on the data that treatment of lipoatrophic or obese diabetic mice with adiponectin or overexpression of adiponectin in ob/ob mice resulted in increased expression levels of PPAR target genes such as CD36, acyl-coenzyme A oxidase, and uncoupling protein 2, we hypothesized that adiponectin could activate PPAR (31) (Fig. 4).
Consistent with this hypothesis, adiponectin indeed increased the expression levels of PPAR in vivo (31). These data suggested that adiponectin increased fatty-acid combustion and energy consumption, presumably via PPAR activation at least in part, which led to decreased TG content in the liver and skeletal muscle and thus coordinately increased in vivo insulin sensitivity.
Endogenous PPAR ligand activities were measured in vitro to further clarify the mechanisms by which adiponectin activated PPAR (31, 43). Interestingly, the treatment of C2C12 myocytes with adiponectin for 6 h significantly increased PPAR ligand activities (43) and at the same time fatty-acid oxidation in vitro.
3. Adiponectin activates AMP kinase.
We next examined the effects of treatment of adiponectin for a shorter time period (51). Treatment of C2C12 myocytes with adiponectin for 1 h stimulated fatty-acid oxidation. Although actinomycin D had no effect on the increase in fatty-acid oxidation stimulated by adiponectin for 1 h, it suppressed fatty-acid oxidation stimulated by the PPAR agonist Wy-14,643. Moreover, treatment of C2C12 myocytes for 1 h stimulated glucose uptake. We hypothesized that adiponectin may stimulate ?-oxidation and glucose uptake via AMP-activated protein kinase (AMPK) during a period shorter than 6 h (51).
Globular adiponectin and full-length adiponectin stimulated phosphorylation and activation of AMPK in skeletal muscle, whereas only full-length adiponectin did so in the liver (51). In parallel with its activation of AMPK, adiponectin stimulated phosphorylation of acetyl coenzyme-A carboxylase (ACC), fatty-acid combustion, glucose uptake, and lactate production in myocytes, and also stimulated phosphorylation of ACC and caused a reduction in molecules involved in gluconeogenesis in the liver, which can account for the acute glucose-lowering effects of adiponectin in vivo (51). Blocking AMPK activation by use of a dominant negative mutant inhibited each of these effects, indicating that stimulation of glucose utilization and fatty-acid combustion by adiponectin occurs through activation of AMPK. Our data may provide a novel paradigm that an adipocyte-derived hormone activates AMPK, thereby directly regulating glucose metabolism and insulin sensitivity in vitro and in vivo (51) (Fig. 4).
The group of Lodish and Ruderman also showed that the adiponectin/ACRP30 globular domain enhanced muscle fat oxidation and glucose transport via AMPK activation and ACC inhibition (52). More recently, AMPK was reported to be involved in glucose uptake stimulated by the globular domain of adiponectin in primary rat adipocytes (53). Because leptin has also been shown to stimulate AMPK in skeletal muscle (54), activation of AMPK may be a common mechanism by which insulin-sensitizing adipokines such as adiponectin and leptin increase insulin sensitivity.
Scherer’s group also reported that in adiponectin transgenic mice, reduced expression of gluconeogenic enzymes such as phosphoenolpyruvate carboxykinase and glucose-6-phosphatase was associated with elevated phosphorylation of AMPK in liver (44). The same group reported that adiponectin is found as two forms in serum, as a lower molecular weight trimer-dimer and a HMW complex (28). Female subjects display significantly higher levels of the HMW complex in serum than do male subjects (23, 28, 55, 56, 57). Levels of the HMW complex appeared to be negatively regulated by insulin. In accordance with this, the amount of HMW adiponectin complex, but not the total amount of adiponectin, was recently reported to be correlated with a thiazolidinedione-mediated improvement in insulin sensitivity (55).
B. Antiatherosclerotic actions
Adiponectin has been reported to have direct antiatherosclerotic effects (58, 59, 60, 61, 62, 63, 64, 65, 66, 67). Adiponectin was demonstrated to strongly inhibit the expression of adhesion molecules, including intracellular adhesion molecule-1, vascular cellular adhesion molecule-1, and E-selectin (Fig. 5). Adiponectin was also shown to inhibit TNF--induced nuclear factor-B activation through the inhibition of IB phosphorylation (61). Suppression of nuclear factor-B by adiponectin might be a major molecular mechanism for the inhibition of monocyte adhesion to endothelial cells (62). Adiponectin also inhibits the expression of the scavenger receptor class A-1 of macrophages, resulting in markedly decreased uptake of oxidized low-density lipoprotein by macrophages and inhibition of foam cell formation (63). In addition, in cultured smooth muscle cells, adiponectin attenuated DNA synthesis induced by growth factors including platelet-derived growth factor, heparin-binding epidermal growth factor (EGF)-like growth factor, basic fibroblast growth factor, and EGF, as well as cell proliferation and migration induced by heparin-binding EGF-like growth factor (64). This inhibition was shown to be attributable to the inhibition of signal transduction through ERK. More recently, selective suppression of endothelial cell apoptosis via AMPK activation by the HMW form of adiponectin has been reported (65).
VI. Alterations in Adiponectin Gene Are Associated with Human Diabetes
Independent of these functional analyses carried out in vitro and in animal models, data from human genetic studies on adiponectin also support the role of adiponectin as a determinant of susceptibility to insulin resistance and type 2 diabetes. By use of affected sib-pair analysis, complete genome mapping of type 2 diabetes genes in Japanese was performed (68). The genome scans revealed at least nine chromosomal regions linked to type 2 diabetes in Japanese people. Among these, three chromosomal regions (3q, 15q, and 20q) are the same regions as previously reported in other ethnic groups. Among these three chromosomal regions, interestingly, the 3q27 chromosomal region contains the adiponectin gene.
We screened for the adiponectin gene and identified 10 relatively common single nucleotide polymorphisms (SNPs) in the Japanese population (Fig. 6). One such SNP, SNP 276 in intron 2 (G vs. T), showed interesting phenotypes with respect to plasma adiponectin levels, insulin resistance, and susceptibility to type 2 diabetes (69) (Fig. 7). Subjects with the G/G genotype had lower plasma adiponectin levels than those with the T/T genotype. Subjects with the G/G genotype at position 276 had a higher insulin resistance index than those with T/T. Importantly, subjects with the G/G genotype at position 276 were at increased risk for type 2 diabetes. The odds ratio was slightly greater than 2 (69) (Fig. 8). Similar associations for the adiponectin gene with susceptibility to type 2 diabetes have also been reported in other ethnic groups (70, 71, 72). In German and American Caucasians, the SNP 276, either independently or as a haplotype together with SNP 45 in exon 2, was shown to be associated with obesity and insulin resistance (71, 72). In French Caucasians, two SNPs in the promoter region of the adiponectin gene, SNP-11377 and SNP-11391, were significantly associated with hypoadiponectinemia and type 2 diabetes (70). Taken together, these data strongly support the hypothesis that adiponectin plays a pivotal role in the pathogenesis of type 2 diabetes.
Several cross-sectional studies have reported that adiponectin levels were decreased in subjects with type 2 diabetes and are inversely correlated with insulin resistance. However, no studies had investigated whether adiponectin protects subjects from diabetes or the extent of risk of developing diabetes in subjects with hypoadiponectinemia. Recently, matched case-control studies in subjects recruited from a large cohort have examined the protective effect of adiponectin against diabetes. One study was performed in severely obese Pima Indian subjects, who have the highest known prevalence of obesity and type 2 diabetes in the world, to assess the role of adiponectin independent of the effects of obesity (73). Subjects with high concentrations of adiponectin were 40% less likely to develop type 2 diabetes than those with low concentrations after adjustment for body mass index (BMI), indicating that adiponectin could be used as a predictor of future development of type 2 diabetes in addition to the established risk parameters, such as BMI.
In addition to the relatively common SNPs, eight mutations in the human adiponectin gene have been reported (69, 74, 75), some of which were significantly related to diabetes and hypoadiponectinemia (23, 75). Among human adiponectin mutations, Arg112Cys and Ile164Thr mutants did not assemble into trimers, which caused impaired secretion from the cell (23). These mutants are clinically associated with hypoadiponectinemia. The Gly84Arg and Gly90Ser mutants were able to assemble into trimers and hexamers but were unable to form HMW multimers (the HMW multimers are thought to be larger than heximers), which are clinically associated with diabetes. These data raised the possibility that HMW multimers have more potent insulin-sensitizing effects than trimers and hexamers (23).
These data suggest that impaired multimerization of adiponectin may be among the causes of a diabetic phenotype or hypoadiponectinemia in subjects having these mutations. Thus, not only the total concentrations but also the multimer distribution should always be considered when interpreting plasma adiponectin levels in health as well as various disease states (23, 24, 25).
VII. Cloning of Adiponectin Receptors AdipoR1 and AdipoR2
We believe that cloning of the adiponectin receptor should facilitate studies on the regulation of glucose and lipid metabolism, the molecular causes of diabetes and atherosclerosis, and the development of antidiabetic and antiatherosclerotic drugs. We isolated cDNA for adiponectin receptors (AdipoR) that mediate the antidiabetic effects from human skeletal muscle cDNA library by screening for globular adiponectin binding (76).
The cDNA analyzed encoded a protein designated human AdipoR1 (Fig. 8) (76). This protein is conserved from yeast to man (especially in the seven transmembrane domains). Interestingly, this yeast homolog YOL002c plays a key role in metabolic pathways that regulate lipid metabolism such as fatty-acid oxidation (77).
Because there may be two distinct adiponectin receptors, we searched for a homologous gene in the human and mouse databases. We found only one gene that was significantly homologous (67% identity in amino acids) to AdipoR1, which was termed AdipoR2 (Fig. 8) (76). AdipoR1 was ubiquitously expressed and most abundantly expressed in skeletal muscle, whereas AdipoR2 was most abundantly expressed in mouse liver. It was reported that adiponectin receptors were expressed in pancreatic ?-cells, and that fatty acids may regulate their expression levels (78). GH is reported to be a positive regulator of AdipoR2 in 3T3-L1 adipocytes (79).
AdipoR1 and AdipoR2 appeared to be integral membrane proteins; the N terminus was internal, and the C terminus was external, which is opposite to the topology of all other reported G protein-coupled receptors (Fig. 8) (76). AdipoR1 and AdipoR2 may form both homo- and heteromultimers. Scatchard plot analysis revealed that AdipoR1 is a receptor for globular adiponectin, whereas AdipoR2 is a receptor for full-length adiponectin (76). Suppression of AdipoR1 with small interfering RNA (siRNA) reduced the increase in fatty-acid oxidation by globular adiponectin. Suppression of AdipoR2 with siRNA reduced the increase in fatty-acid oxidation by full-length adiponectin (Fig. 9) (76).
Thus, we have isolated cDNA-encoding adiponectin receptors (AdipoR1 and R2). Expression of AdipoR1/R2 or suppression of AdipoR1/R2 supports our conclusion that AdipoR1 and R2 serve as receptors for globular and full-length adiponectin and mediate increased AMPK, PPAR ligand activities and fatty-acid oxidation and glucose uptake by adiponectin (Fig. 9) (57).
Lodish’s group reported that T-cadherin was capable of binding adiponectin in C2C12 myoblasts, but not in the liver or hepatocytes (80).
VIII. Regulation of Adiponectin Receptors
A. Regulation of expression levels of AdipoR1 and AdipoR2
We first examined whether the expressions of AdipoR1 and/or AdipoR2 were regulated under physiological and/or pathophysiological states (81). The levels of AdipoR1 and AdipoR2 mRNA expression in the liver and skeletal muscle increased after fasting, and refeeding rapidly restored these to levels equal to the original fed state. AdipoR1 and AdipoR2 mRNA increased significantly in skeletal muscle of mice rendered hypoinsulinemic/hyperglycemic with streptozotocin, and both AdipoR1 and AdipoR2 mRNA were almost completely restored by insulin treatment. These observations suggested that insulin may negatively regulate AdipoR1/R2 mRNA levels (81). The PI3-kinase inhibitor LY 294002 and constitutively active form of Foxo (Forkhead box, class O) 1 revealed that insulin repressed AdipoR1/R2 mRNA expressions via activation of PI3-kinase and inactivation of Foxo1 (81).
The expressions of both AdipoR1 and AdipoR2 were significantly decreased in muscle and adipose tissue of insulin-resistant ob/ob mice, which exhibited hyperglycemia and hyperinsulinemia, as compared with control mice (81) (Fig. 10). Scatchard plot analysis revealed that both high-affinity and low-affinity binding sites for globular adiponectin (gAd) and adiponectin binding in skeletal muscles of ob/ob mice were reduced as compared with those of wild-type mice, findings that are consistent with the fact that the numbers of both AdipoR1 and AdipoR2 were reduced. Moreover, adiponectin-induced activation of AMPK was impaired in skeletal muscle of ob/ob mice. These data suggest that adiponectin resistance was observed in ob/ob mice, which exhibited decreased expression levels of AdipoR1 and AdipoR2 (81) (Fig. 10).
We and others have previously shown that plasma adiponectin levels were decreased in obesity. This reduction may play a causal role in the development of insulin resistance. In the same study, we have also shown that obesity decreased the expression levels of AdipoR1/R2, thereby reducing adiponectin sensitivity, which finally leads to insulin resistance, the so-called "vicious cycle" (61) (Fig. 10).
A correlation has been reported between adiponectin receptor gene expression and insulin sensitivity in nondiabetic Mexican Americans with or without a family history of type 2 diabetes (82). Adiponectin receptor expression in skeletal muscle of type 2 diabetic patients was also reported to be decreased (83).
Our data suggest that not only agonism of AdipoR1/R2 but also strategies to increase AdipoR1/R2 may be a logical approach with which to provide a novel treatment modality for insulin resistance and type 2 diabetes.
IX. Adiponectin Hypothesis
Based upon the significant body of evidence discussed in this review, obtained from our and other laboratories, we propose the following adiponectin hypothesis (Fig. 11). Reduced adiponectin levels were caused by interactions of genetic factors such as SNPs in the adiponectin gene itself and environmental factors causing obesity such as a HF diet. Reduced adiponectin actions also resulted from down-regulation of adiponectin receptors linked to obesity. These reductions of adiponectin actions may play a crucial causal role in the development of insulin resistance, type 2 diabetes, metabolic syndrome, and atherosclerosis (Fig. 11).
X. Adiponectin and Adiponectin Receptors as Therapeutic Targets
According to our adiponectin hypothesis, a therapeutic strategy for type 2 diabetes, metabolic syndrome, and cardiovascular diseases may include the up-regulation of plasma adiponectin, up-regulation of adiponectin receptors, or the development of AdipoRs agonists.
A. Up-regulation of plasma adiponectin
Insulin sensitizer PPAR agonists have been shown to increase adiponectin levels in mice (31) and humans (84), as well as in 3T3L1 adipocytes in vitro (31). These effects seem to be associated with small-sized adipocytes (39), adipocytes differentiation (85, 86), direct transcriptional activation of genes via peroxisome proliferator response element (87, 88, 89, 90, 91), and increased insulin action (92). Interestingly, both PPAR agonists and adiponectin have been shown to increase insulin sensitivity and ameliorate atherosclerosis. To test whether the PPAR agonist-mediated improvement in insulin sensitivity and/or amelioration of atherosclerosis was dependent on adiponectin is very important, and thus it is very interesting to see the effects of PPAR agonists in adiponectin knockout mice.
B. Up-regulation of adiponectin receptors and development of AdipoRs agonists
The evidence described in this review indicates that reductions in plasma adiponectin levels and adiponectin receptors may play major roles in the development of insulin resistance, type 2 diabetes, metabolic syndrome, and cardiovascular diseases that are linked to obesity. With this in mind, one therapeutic strategy may be to up-regulate plasma adiponectin levels, which has already been discussed. The other strategy may be to up-regulate adiponectin receptors or to stimulate adiponectin receptors using small molecule agonists. We would like to introduce two interesting examples of attempts to develop such drugs.
Dr. Staels’ group reported that adiponectin receptors are expressed in human macrophages and that their expression levels may be regulated by agonists of the nuclear receptors PPAR, PPAR, and liver X receptor (93).
Osmotin is a pathogenesis-related (PR)-5 family of plant defense proteins that induces apoptosis in the yeast. Dr. Bressan’s group at Purdue University isolated and selected yeast clones that exhibited hypersensitivity to osmotin, sequenced their cDNA inserts, and found that PHO36/YOL002c, the yeast homolog of AdipoR, is a receptor for osmotin (94) (Fig. 12).
X-ray crystallographic studies revealed that both globular adiponectin and osmotin consist of antiparallel ?-strands arranged in the shape of a ?-barrel. The domain I (lectin-like domain) of osmotin can be overlapped with adiponectin, suggesting that the two proteins share the lectin-like domain (94) (Fig. 12).
Interestingly, osmotin could activate AMP kinase in C2C12 myocytes. More importantly, suppression of AdipoRs expression by siRNA markedly reduced phosphorylation of AMP kinase induced by osmotin. These data suggest that osmotin activates AMP kinase via AdipoRs in mammalian C2C12 myocytes (94).
Osmotin is a member of a large PR-5 protein family, which is both ubiquitous (fruits and vegetables, etc.) and diverse. PR-5 proteins are also extremely stable and may remain active even when in contact with the human digestive or respiratory systems. Osmotin, which is a ligand for the yeast homolog of AdipoR (PHO36), activates AMP kinase via AdipoR in C2C12 myocytes. These data raise the possibility that further research examining similarities in adiponectin and osmotin may facilitate the development of potential adiponectin receptor agonists (94).
C. Pleiotropic effects of adiponectin in relation to metabolic syndrome
In this review, we have stated that adiponectin increases insulin sensitivity in the liver and skeletal muscle and that adiponectin also reduces atherosclerosis. In addition to these effects, adiponectin also seems to have pleiotropic effects, particularly in relation to metabolic syndrome. Obesity has been reported to be associated with a higher incidence of certain cancers. Recently, adiponectin was reported to induce antiangiogenesis and antitumor activity via caspase-mediated endothelial cell apoptosis (95). Moreover, fatty liver and/or liver fibrosis are often associated with metabolic syndrome. Adiponectin was reported to alleviate alcoholic and nonalcoholic fatty liver diseases (96, 97) and liver fibrosis (98) in mice. Furthermore, it is possible that adiponectin stimulates insulin secretion and/or regulates energy homeostasis (99, 100). Further studies will be needed to determine the physiological and pathophysiological roles of AdipoR1 and AdipoR2 in these actions.
Acknowledgments
We thank Drs. R. Nagai, T. Shimizu, T. Yokomizo, K. Taira, M. Miyagishi, T. Kitamura, K. Tobe, K. Ueki, Y. Terauchi, K. Hara, N. Kubota, T. Sugiyama, J. Kamon, H. Waki, Y. Hada, S. Takekawa, A. Tsuchida, Y. Itoh, T. Maki, M. Kobayashi, K. Takasawa, S. Uchida, S. Kita, M. Noda, K. Eto, R. Suzuki, Y. Kaburagi, H. Kagechika, K. Shudo, (University of Tokyo), P. Froguel (Imperial College; UK), K. Komeda (Tokyo Medical University), Y. Akanuma and K. Kosaka (Institute for Diabetes Care and Research, Asahi Life Foundation), K. Murakami (Kyorin Pharmaceutical), Y. Oike (Keio University), and Y. Ueyama (Tokai University and Central Institute for Experimental Animals) for their helpful suggestions. We are grateful to A. Okano, A. Itoh, K. Miyata, S. Nakamura, Y. Mizuno, C. Katayama, and K. Nitta for their excellent technical assistance.
Footnotes
This work was supported by the Program for Promotion of Fundamental Studies in Health Sciences of the Organization for Pharmaceutical Safety and Research of Japan, a grant from the Human Science Foundation (to T.K.); a Grant-in-Aid for the Development of Innovative Technology from the Ministry of Education, Culture, Sports, Science and Technology of Japan (to T.K.); a Grant-in Aid for Creative Scientific Research (10NP0201) from the Japan Society for the Promotion of Science (to T.K.); and Health Science Research Grants (Research on Human Genome and Gene Therapy) from the Ministry of Health, Labor and Welfare of Japan (to T.K.).
Abbreviations: ACC, Acetyl-coenzyme-A carboxylase; AMPK, AMP-activated protein kinase; apoE, apolipoprotein E; EGF, epidermal growth factor; gAd, globular adiponectin; HF, high-fat; HMW, high molecular weight; PI, phosphatidylinositol; PPAR, peroxisome proliferator-activated receptor; PR, pathogenesis-related; siRNA, small interfering RNA; SNP, single nucleotide polymorphism; TG, triglyceride.
References
Spiegelman BM, Flier JS 1996 Adipogenesis and obesity: rounding out the big picture. Cell 87:377–389
Reaven GM 1995 The fourth Musketeer—from Alexandre Dumas to Claude Bernard. Diabetologia 38:3–13
Shulman GI 2000 Cellular mechanisms of insulin resistance. J Clin Invest 106:171–176
White RT, Damm D, Hancock N, Rosen BS, Lowell BB, Usher P, Flier JS, Spiegelman BM 1992 Human adipsin is identical to complement factor D and is expressed at high levels in adipose tissue. J Biol Chem 267:9210–9213
Friedman JM 2000 Obesity in the new millennium. Nature 404:632–634
Shimomura I, Funahashi T, Takahashi M, Maeda K, Kotani K, Nakamura T, Yamashita S, Miura M, Fukuda Y, Takemura K, Tokunaga K, Matsuzawa Y 1996 Enhanced expression of PAI-1 in visceral fat: possible contributor to vascular disease in obesity. Nat Med 2:800–803
Steppan CM, Bailey ST, Bhat S, Brown EJ, Banerjee RR, Wright CM, Patel HR, Ahima RS, Lazar MA 2001 The hormone resistin links obesity to diabetes. Nature 409:307–312
Hotamisligil GS 1999 The role of TNF and TNF receptors in obesity and insulin resistance. J Intern Med 245:621–625
Beltowski J 2003 Adiponectin and resistin—new hormones of white adipose tissue. Med Sci Monit 9:RA55–RA61
Vasseur F, Lepretre F, Lacquemant C, Froguel P 2003 The genetics of adiponectin. Curr Diab Rep 3:151–158
Heilbronn LK, Smith SR, Ravussin E 2003 The insulin-sensitizing role of the fat derived hormone adiponectin. Curr Pharm Des 9:1411–1418
Wolf G 2003 Adiponectin: a regulator of energy homeostasis. Nutr Rev 61:290–292
Haluzik M, Parizkova J, Haluzik MM 2004 Adiponectin and its role in the obesity-induced insulin resistance and related complications. Physiol Res 53:123–129
Ukkola O, Santaniemi M 2002 Adiponectin: a link between excess adiposity and associated comorbidities? J Mol Med 80:696–702
Scherer PE, Williams S, Fogliano M, Baldini G, Lodish HF 1995 A novel serum protein similar to C1q, produced exclusively in adipocytes. J Biol Chem 270:26746–26749
Hu E, Liang P, Spiegelman BM 1996 AdipoQ is a novel adipose-specific gene dysregulated in obesity. J Biol Chem 271:10697–10703
Maeda K, Okubo K., Shimomura I, Funahashi T, Matsuzawa Y, Matsubara K 1996 cDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (AdiPose Most abundant Gene transcript 1). Biochem Biophys Res Commun 221:286–289
Nakano Y, Tobe T, Choi-Miura NH, Mazda T, Tomita M 1996 Isolation and characterization of GBP28, a novel gelatin-binding protein purified from human plasma. J Biochem (Tokyo) 120:803–812
Crouch E, Persson A, Chang D, Heuser J 1994 Molecular structure of pulmonary surfactant protein D (SP-D). J Biol Chem 269:17311–17319
McCormack FX, Pattanajitvilai S, Stewart J, Possmayer F, Inchley K, Voelker DR 1997 The Cys6 intermolecular disulfide bond and the collagen-like region of rat SP-A play critical roles in interactions with alveolar type II cells and surfactant lipids. J Biol Chem 272:27971–27979
Wong GW, Wang J, Hug C, Tsao TS, Lodish HF 2004 A family of Acrp30/adiponectin structural and functional paralogs. Proc Natl Acad Sci USA 101:10302–10307
Shapiro L, Scherer PE 1998 The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor. Curr Biol 8:335–340
Waki H, Yamauchi T, Kamon J, Ito Y, Uchida S, Kita S, Hara K, Hada Y, Vasseur F, Froguel P, Kimura S, Nagai R, Kadowaki T 2003 Impaired multimerization of human adiponectin mutants associated with diabetes: Molecular structure and multimer formation of adiponectin. J Biol Chem 278:40352–40363
Tsao T-S, Murrey HE, Hug C, Lee DH, Lodish HF 2002 Oligomerization state-dependent activation of NF-B signaling pathway by adipocyte complement-related protein of 30 kDa(Acrp30). J Biol Chem 277:29359–29362
Tsao TS, Tomas E, Murrey HE, Hug C, Lee DH, Ruderman NB, Heuser JE, Lodish HF 2003 Role of disulfide bonds in Acrp30/adiponectin structure and signaling specificity. Different oligomers activate different signal transduction pathways. J Biol Chem 278:50810–50817
Fruebis J, Tsao TS, Javorschi S, Ebbets-Reed D, Erickson MR, Yen FT, Bihain BE, Lodish HF 2001 Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice. Proc Natl Acad Sci USA 98:2005–2010
Waki H, Yamauchi T, Kamon J, Kita S, Ito Y, Hada Y, Uchida S, Tsuchida A, Takekawa S, Kadowaki T 2005 Generation of globular fragment of adiponectin by leukocyte elastase secreted by monocytic cell line THP-1. Endocrinology 146:790–796
Pajvani UB, Du X, Combs TP, Berg AH, Rajala MW, Schulthess T, Engel J, Brownlee M, Scherer PE 2003 Structure-function studies of the adipocyte-secreted hormone Acrp30/adiponectin. Implications for metabolic regulation and bioactivity. J Biol Chem 278:9073–9085
Wang Y, Xu A, Knight C, Xu LY, Cooper GJ 2002 Hydroxylation and glycosylation of the four conserved lysine residues in the collagenous domain of adiponectin. Potential role in the modulation of its insulin-sensitizing activity. J Biol Chem 277:19521–19529
Sato C, Yasukawa Z, Honda N, Matsuda T, Kitajima K 2001 Identification and adipocyte differentiation-dependent expression of the unique disialic acid residue in an adipose tissue-specific glycoprotein, adipo Q. J Biol Chem 276:28849–28856
Yamauchi T, Kamon J, Waki H, Terauchi Y, Kubota N, Hara K, Mori Y, Ide T, Murakami K, Tsuboyama-Kasaoka N, Ezaki O, Akanuma Y, Gavrilova O, Vinson C, Reitman ML, Kagechika H, Shudo K, Yoda M, Nakano Y, Tobe K, Nagai R, Kimura S, Tomita M, Froguel P, Kadowaki T 2001 The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med 7:941–946
Arita Y, Kihara S, Ouchi N, Takahashi M, Maeda K, Miyagawa J, Hotta K, Shimomura I, Nakamura T, Miyaoka K, Kuriyama H, Nishida M, Yamashita S, Okubo K, Matsubara K, Muraguchi M, Ohmoto Y, Funahashi T, Matsuzawa Y 1999 Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity. Biochem Biophys Res Commun 257:79–83
Hotta K, Funahashi T, Arita Y, Takahashi M, Matsuda M, Okamoto Y, Iwahashi H, Kuriyama H, Ouchi N, Maeda K, Nishida M, Kihara S, Sakai N, Nakajima T, Hasegawa K, Muraguchi M, Ohmoto Y, Nakamura T, Yamashita S, Hanafusa T, Matsuzawa Y 2000 Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients. Arterioscler Thromb Vasc Biol 20:1595–1599
Kumada M, Kihara S, Sumitsuji S, Kawamoto T, Matsumoto S, Ouchi N, Arita Y, Okamoto Y, Shimomura I, Hiraoka H, Nakamura T, Funahashi T, Matsuzawa Y; Osaka CAD Study Group 2003 Association of hypoadiponectinemia with coronary artery disease in men. Arterioscler Thromb Vasc Biol 23:85–89
Ouchi N, Ohishi M, Kihara S, Funahashi T, Nakamura T, Nagaretani H, Kumada M, Ohashi K, Okamoto Y, Nishizawa H, Kishida K, Maeda N, Nagasawa A, Kobayashi H, Hiraoka H, Komai N, Kaibe M, Rakugi H, Ogihara T, Matsuzawa Y 2003 Association of hypoadiponectinemia with impaired vasoreactivity. Hypertension 42:231–234
Trujillo ME, Scherer PE 2005 Adiponectin: journey from an adipocyte secretory protein to biomarker of the metabolic syndrome. J Intern Med 257:167–175
Berg AH, Combs TP, Du X, Brownlee M, Scherer PE 2001 The adipocyte-secreted protein Acrp30 enhances hepatic insulin action. Nat Med 7:947–953
Kubota N, Terauchi Y, Miki H, Tamemoto H, Yamauchi T, Komeda K, Satoh S, Nakano R, Ishii C, Sugiyama T, Eto K, Tsubamoto Y, Okuno A, Murakami K, Sekihara H, Hasegawa G, Naito M, Toyoshima Y, Tanaka S, Shiota K, Kitamura T, Fujita T, Ezaki O, Aizawa S, Nagai R, Tobe K, Kimura S, Kadowaki T 1999 PPAR mediates high-fat diet-induced adipocyte hypertrophy and insulin resistance. Mol Cell 4:597–609
Yamauchi T, Kamon J, Waki H, Murakami K, Motojima K, Komeda K, Ide T, Kubota N, Terauchi Y, Tobe K, Miki H, Tsuchida A, Akanuma Y, Nagai R, Kimura S, Kadowaki T 2001 The mechanisms by which both heterozygous PPAR deficiency and PPAR agonist improve insulin resistance. J Biol Chem 276:41245–41254
Shimomura I, Hammer RE, Ikemoto S, Brown MS, Goldstein JL 1999 Leptin reverses insulin resistance and diabetes mellitus in mice with congenital lipodystrophy. Nature 401:73–76
Yamauchi T, Waki H, Kamon J, Murakami K, Motojima K, Komeda K, Miki H, Kubota N, Terauchi Y, Tsuchida A, Tsuboyama-Kasaoka N, Yamauchi N, Ide T, Hori W, Kato S, Fukayama M, Akanuma Y, Ezaki O, Itai A, Nagai R, Kimura S, Tobe K, Kagechika H, Shudo K, Kadowaki T 2001 Inhibition of RXR and PPAR ameliorates diet-induced obesity and type 2 diabetes. J Clin Invest 108:1001–1013
Combs TP, Berg AH, Obici S, Scherer PE, Rossetti L 2001 Endogenous glucose production is inhibited by the adipose-derived protein Acrp30. J Clin Invest 108:1875–1881
Yamauchi T, Kamon J, Waki H, Imai Y, Shimozawa N, Hioki K, Uchida S, Ito Y, Takakuwa K, Matsui J, Takata M, Eto K, Terauchi Y, Komeda K, Tsunoda M, Murakami K, Ohnishi Y, Naitoh T, Yamamura K, Ueyama Y, Froguel P, Kimura S, Nagai R, Kadowaki T 2003 Globular adiponectin protected ob/ob mice from diabetes and apoE-deficient mice from atherosclerosis. J Biol Chem 278:2461–2468
Combs TP, Pajvani UB, Berg AH, Lin Y, Jelicks LA, Laplante M, Nawrocki AR, Rajala MW, Parlow AF, Cheeseboro L, Ding YY, Russell RG, Lindemann D, Hartley A, Baker GR, Obici S, Deshaies Y, Ludgate M, Rossetti L, Scherer PE 2004 A transgenic mouse with a deletion in the collagenous domain of adiponectin displays elevated circulating adiponectin and improved insulin sensitivity. Endocrinology 145:367–383
Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, Eto K, Yamashita T, Kamon J, Satoh H, Yano W, Nagai R, Kimura S, Kadowaki T, Noda T 2002 Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem 277:25863–25866
Maeda N, Shimomura I, Kishida K, Nishizawa H, Matsuda M, Nagaretani H, Furuyama N, Kondo H, Takahashi M, Arita Y, Komuro R, Ouchi N, Kihara S, Tochino Y, Okutomi K, Horie M, Takeda S, Aoyama T, Funahashi T, Matsuzawa Y 2002 Diet-induced insulin resistance in mice lacking adiponectin/ACRP30. Nat Med 8:731–737
Ma K, Cabrero A, Saha PK, Kojima H, Li L, Chang BH, Paul A, Chan L 2002 Increased ?-oxidation but no insulin resistance or glucose intolerance in mice lacking adiponectin. J Biol Chem 277:34658–34661
Shklyaev S, Aslanidi G, Tennant M, Prima V, Kohlbrenner E, Kroutov V, Campbell-Thompson M, Crawford J, Shek EW, Scarpace PJ, Zolotukhin S 2003 Sustained peripheral expression of transgene adiponectin offsets the development of diet-induced obesity in rats. Proc Natl Acad Sci USA 100:14217–14222
Okamoto Y, Kihara S, Ouchi N, Nishida M, Arita Y, Kumada M, Ohashi K, Sakai N, Shimomura I, Kobayashi H, Terasaka N, Inaba T, Funahashi T, Matsuzawa Y 2002 Adiponectin reduces atherosclerosis in apolipoprotein E-deficient mice. Circulation 106:2767–2770
Matsuda M, Shimomura I, Sata M, Arita Y, Nishida M, Maeda N, Kumada M, Okamoto Y, Nagaretani H, Nishizawa H, Kishida K, Komuro R, Ouchi N, Kihara S, Nagai R, Funahashi T, Matsuzawa Y 2002 Role of adiponectin in preventing vascular stenosis. The missing link of adipo-vascular axis. J Biol Chem 277:37487–37491
Yamauchi T, Kamon J, Minokoshi Y, Ito Y, Waki H, Uchida S, Yamashita S, Noda M, Kita S, Ueki K, Eto K, Akanuma Y, Froguel P, Foufelle F, Ferre P, Carling D, Kimura S, Nagai R, Kahn BB, Kadowaki T 2002 Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase. Nat Med 8:1288–1295
Tomas E, Tsao TS, Saha AK, Murrey HE, Zhang Cc C, Itani SI, Lodish HF, Ruderman NB 2002 Enhanced muscle fat oxidation and glucose transport by ACRP30 globular domain: acetyl-CoA carboxylase inhibition and AMP-activated protein kinase activation. Proc Natl Acad Sci USA 99:16309–16313
Wu X, Motoshima H, Mahadev K, Stalker TJ, Scalia R, Goldstein BJ 2003 Involvement of AMP-activated protein kinase in glucose uptake stimulated by the globular domain of adiponectin in primary rat adipocytes. Diabetes 52:1355–1363
Minokoshi Y, Kim YB, Peroni OD, Fryer LG, Muller C, Carling D, Kahn BB 2002 Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase. Nature 415:339–343
Pajvani UB, Hawkins M, Combs TP, Rajala MW, Doebber T, Berger JP, Wagner JA, Wu M, Knopps A, Xiang AH, Utzschneider KM, Kahn SE, Olefsky JM, Buchanan TA, Scherer PE 2004 Complex distribution, not absolute amount of adiponectin, correlates with thiazolidinedione-mediated improvement in insulin sensitivity. J Biol Chem 279:12152–12162
Nishizawa H, Shimomura I, Kishida K, Maeda N, Kuriyama H, Nagaretani H, Matsuda M, Kondo H, Furuyama N, Kihara S, Nakamura T, Tochino Y, Funahashi T, Matsuzawa Y 2002 Androgens decrease plasma adiponectin, an insulin-sensitizing adipocyte-derived protein. Diabetes 51:2734–2741
Combs TP, Berg AH, Rajala MW, Klebanov S, Iyengar P, Jimenez-Chillaron JC, Patti ME, Klein SL, Weinstein RS, Scherer PE 2003 Sexual differentiation, pregnancy, calorie restriction, and aging affect the adipocyte-specific secretory protein adiponectin. Diabetes 52:268–276
Matsuzawa Y, Shimomura I, Kihara S, Funahashi T 2003 Importance of adipocytokines in obesity-related diseases. Horm Res 60(Suppl 3):56–59
Matsuzawa Y, Funahashi T, Kihara S, Shimomura I 2004 Adiponectin and metabolic syndrome. Arterioscler Thromb Vasc Biol 24:29–33
Funahashi T, Nakamura T, Shimomura I, Maeda K, Kuriyama H, Takahashi M, Arita Y, Kihara S, Matsuzawa Y 1999 Role of adipocytokines on the pathogenesis of atherosclerosis in visceral obesity. Intern Med 38:202–206
Ouchi N, Kihara S, Arita Y, Okamoto Y, Maeda K, Kuriyama H, Hotta K, Nishida M, Takahashi M, Muraguchi M, Ohmoto Y, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 2000 Adiponectin, an adipocyte-derived plasma protein, inhibits endothelial NF-B signaling through a cAMP-dependent pathway. Circulation 102:1296–1301
Ouchi N, Kihara S, Arita Y, Maeda K, Kuriyama H, Okamoto Y, Hotta K, Nishida M, Takahashi M, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 1999 Novel modulator for endothelial adhesion molecules: adipocyte-derived plasma protein adiponectin. Circulation 100:2473–2476
Ouchi N, Kihara S, Arita Y, Nishida M, Matsuyama A, Okamoto Y, Ishigami M, Kuriyama H, Kishida K, Nishizawa H, Hotta K, Muraguchi M, Ohmoto Y, Yamashita S, Funahashi T, Matsuzawa Y 2001 Adipocyte-derived plasma protein, adiponectin, suppresses lipid accumulation and class A scavenger receptor expression in human monocyte-derived macrophages. Circulation 103:1057–1063
Arita Y, Kihara S, Ouchi N, Maeda K, Kuriyama H, Okamoto Y, Kumada M, Hotta K, Nishida M, Takahashi M, Nakamura T, Shimomura I, Muraguchi M, Ohmoto Y, Funahashi T, Matsuzawa Y 2002 Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB-binding protein and regulates growth factor-induced common postreceptor signal in vascular smooth muscle cell. Circulation 105:2893–2898
Kobayashi H, Ouchi N, Kihara S, Walsh K, Kumada M, Abe Y, Funahashi T, Matsuzawa Y 2004 Selective suppression of endothelial cell apoptosis by the high molecular weight form of adiponectin. Circ Res 94:e27–e31
Chen H, Montagnani M, Funahashi T, Shimomura I, Quon MJ 2003 Adiponectin stimulates production of nitric oxide in vascular endothelial cells. J Biol Chem 278:45021–45026
Kumada M, Kihara S, Ouchi N, Kobayashi H, Okamoto Y, Ohashi K, Maeda K, Nagaretani H, Kishida K, Maeda N, Nagasawa A, Funahashi T, Matsuzawa Y 2004 Adiponectin specifically increased tissue inhibitor of metalloproteinase-1 through interleukin-10 expression in human macrophages. Circulation 109:2046–2049
Mori Y, Otabe S, Dina C, Yasuda K, Populaire C, Lecoeur C, Vatin V, Durand E, Hara K, Okada T, Tobe K, Boutin P, Kadowaki T, Froguel P 2002 Genome-wide search for type 2 diabetes in japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p. Diabetes 51:1247–1255
Hara K, Boutin P, Mori Y, Tobe K, Dina C, Yasuda K, Yamauchi T, Otabe S, Okada T, Eto K, Kadowaki H, Hagura R, Akanuma Y, Yazaki Y, Nagai R, Taniyama M, Matsubara K, Yoda M, Nakano Y, Tomita M, Kimura S, Ito C, Froguel P, Kadowaki T 2002 Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the japanese population. Diabetes 51:536–540
Vasseur F, Helbecque N, Dina C, Lobbens S, Delannoy V, Gaget S, Boutin P, Vaxillaire M, Lepretre F, Dupont S, Hara K, Clement K, Bihain B, Kadowaki T, Froguel P 2002 Single-nucleotide polymorphism haplotypes in the both proximal promoter and exon 3 of the APM1 gene modulate adipocyte-secreted adiponectin hormone levels and contribute to the genetic risk for type 2 diabetes in French Caucasians. Hum Mol Genet 11:2607–2614
Stumvoll M, Tschritter O, Fritsche A, Staiger H, Renn W, Weisser M, Machicao F, Haring H 2002 Association of the T-G polymorphism in adiponectin (exon 2) with obesity and insulin sensitivity: interaction with family history of type 2 diabetes. Diabetes 51:37–41
Menzaghi C, Ercolino T, Paola RD, Berg AH, Waaram JH, Scherer PE, Trischitta V, Doria A 2002 A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome. Diabetes 51:2306–2312
Lindsay RS, Funahashi T, Hanson RL, Matsuzawa Y, Tanaka S, Tataranni PA, Knowler WC, Krakoff J 2002 Adiponectin and development of type 2 diabetes in the Pima Indian population. Lancet 360:57–58
Takahashi M, Arita Y, Yamagata K, Matsukawa Y, Okutomi K, Horie M, Shimomura I, Hotta K, Kuriyama H, Kihara S, Nakamura T, Yamashita S, Funahashi T, Matsuzawa Y 2000 Genomic structure and mutations in adipose-specific gene, adiponectin. Int J Obes Relat Metab Disord 24:861–868
Kondo H, Shimomura I, Matsukawa Y, Kumada M, Takahashi M, Matsuda M, Ouchi N, Kihara S, Kawamoto T, Sumitsuji S, Funahashi T, Matsuzawa Y 2002 Association of adiponectin mutation with type 2 diabetes: a candidate gene for the insulin resistance syndrome. Diabetes 51:2325–2328
Yamauchi T, Kamon J, Ito Y, Tsuchida A, Yokomizo T, Kita S, Sugiyama T, Miyagishi M, Hara, K, Tsunoda M, Murakami K, Ohteki T, Uchida S, Takekawa S, Waki H, Tsuno NH, Shibata Y, Terauchi Y, Froguel P, Tobe K, Koyasu S, Taira K, Kitamura T, Shimizu T, Nagai R, Kadowaki T 2003 Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature [Erratum (2004) 431:1123] 423:762–769
Karpichev IV, Cornivelli L, Small GM 2002 Multiple regulatory roles of a novel Saccharomyces cerevisiae protein, encoded by YOL002c, in lipid and phosphate metabolism. J Biol Chem 277:12152–12162
Kharroubi I, Rasschaert J, Eizirik DL, Cnop M 2003 Expression of adiponectin receptors in pancreatic ? cells. Biochem Biophys Res Commun 312:1118–1122
Fasshauer M, Klein J, Kralisch S, Klier M, Lossner U, Bluher M, Paschke R 2004 Growth hormone is a positive regulator of adiponectin receptor 2 in 3T3–L1 adipocytes. FEBS Lett 558:27–32
Hug C, Wang J, Ahmad NS, Bogan JS, Tsao TS, Lodish HF 2004 T-cadherin is a receptor for hexameric and high-molecular-weight forms of Acrp30/adiponectin. Proc Natl Acad Sci USA 101:10308–10313
Tsuchida A, Yamauchi T, Ito Y, Hada Y, Maki T, Takekawa S, Kamon J, Kobayashi M, Suzuki R, Hara K, Kubota N, Terauchi Y, Froguel P, Nakae J, Kasuga M, Accili D, Tobe K, Ueki K, Nagai R, Kadowaki T 2004 Insulin/Foxo1 pathway regulates expression levels of adiponectin receptors and adiponectin sensitivity. J Biol Chem 279:30817–30822
Civitarese AE, Jenkinson CP, Richardson D, Bajaj M, Cusi K, Kashyap S, Berria R, Belfort R, DeFronzo RA, Mandarino LJ, Ravussin E 2004 Adiponectin receptors gene expression and insulin sensitivity in non-diabetic Mexican Americans with or without a family history of type 2 diabetes. Diabetologia 47:816–820
Debard C, Laville M, Berbe V, Loizon E, Guillet C, Morio-Liondore B, Boirie Y, Vidal H 2004 Expression of key genes of fatty acid oxidation, including adiponectin receptors, in skeletal muscle of type 2 diabetic patients. Diabetologia 47:917–925
Hirose H, Kawai T, Yamamoto Y, Taniyama M, Tomita M, Matsubara K, Okazaki Y, Ishii T, Oguma Y, Takei I, Saruta T 2002 Effects of pioglitazone on metabolic parameters, body fat distribution, and serum adiponectin levels in Japanese male patients with type 2 diabetes. Metabolism 51:314–317
Das K, Lin Y, Widen E, Zhang Y, Scherer PE 2001 Chromosomal localization, expression pattern, and promoter analysis of the mouse gene encoding adipocyte-specific secretory protein Acrp30. Biochem Biophys Res Commun 280:1120–1129
Saito K, Tobe T, Yoda M, Nakano Y, Choi-Miura NH, Tomita M 1999 Regulation of gelatin-binding protein 28 (GBP28) gene expression by C/EBP. Biol Pharm Bull 22:1158–1162
Iwaki M, Matsuda M, Maeda N, Funahashi T, Matsuzawa Y, Makishima M, Shimomura I 2003 Induction of adiponectin, a fat-derived antidiabetic and antiatherogenic factor, by nuclear receptors. Diabetes 52:1655–1663
Maeda N, Takahashi M, Funahashi T, Kihara S, Nishizawa H, Kishida K, Nagaretani H, Matsuda M, Komuro R, Ouchi N, Kuriyama H, Hotta K, Nakamura T, Shimomura I, Matsuzawa Y 2001 PPAR ligands increase expression and plasma concentrations of adiponectin, an adipose-derived protein. Diabetes 50:2094–2099
Bouskila M, Pajvani UB, Scherer PE 2005 Adiponectin: a relevant player in PPAR-agonist-mediated improvements in hepatic insulin sensitivity? Int J Obes Relat Metab Disord 29(Suppl 1):S17–23
Tonelli J, Li W, Kishore P, Pajvani UB, Kwon E, Weaver C, Scherer PE, Hawkins M 2004 Mechanisms of early insulin-sensitizing effects of thiazolidinediones in type 2 diabetes. Diabetes 53:1621–1629
Combs TP, Wagner JA, Berger J, Doebber T, Wang WJ, Zhang BB, Tanen M, Berg AH, O’Rahilly S, Savage DB, Chatterjee K, Weiss S, Larson PJ, Gottesdiener KM, Gertz BJ, Charron MJ, Scherer PE, Moller DE 2002 Induction of adipocyte complement-related protein of 30 kilodaltons by PPAR agonists: a potential mechanism of insulin sensitization. Endocrinology 143:998–1007
Terauchi Y, Matsui J, Kamon J, Yamauchi T, Kubota N, Komeda K, Aizawa S, Akanuma Y, Tomita M, Kadowaki T 2004 Increased serum leptin protects from adiposity despite the increased glucose uptake in white adipose tissue in mice lacking p85 phosphoinositide 3-kinase. Diabetes 53:2261–2270
Chinetti G, Zawadski C, Fruchart JC, Staels B 2004 Expression of adiponectin receptors in human macrophages and regulation by agonists of the nuclear receptors PPAR, PPAR, and LXR. Biochem Biophys Res Commun 314:151–158
Narasimhan LM, Coca MA, Jin J, Yamauchi T, Ito Y, Kadowaki T, Kim KK, Pardo JM, Damsz B, Bressan RA, Yun DJ 2005 Osmotin is a homolog of mammalian adiponectin and controls apoptosis in yeast through a homolog of mammalian adiponectin receptor. Mol Cell 17:171–180
Brakenhielm E, Veitonmaki N, Cao R, Kihara S, Matsuzawa Y, Zhivotovsky B, Funahashi T, Cao Y 2004 Adiponectin-induced antiangiogenesis and antitumor activity involve caspase-mediated endothelial cell apoptosis. Proc Natl Acad Sci USA 101:2476–2481
Xu A, Wang Y, Keshaw H, Xu LY, Lam KS, Cooper GJ 2003 The fat-derived hormone adiponectin alleviates alcoholic and nonalcoholic fatty liver diseases in mice. J Clin Invest 112:91–100
Yoda-Murakami M, Taniguchi M, Takahashi K, Kawamata S, Saito K, Choi-Miura NH, Tomita M 2001 Change in expression of GBP28/adiponectin in carbon tetrachloride-administrated mouse liver. Biochem Biophys Res Commun 285:372–377
Kamada Y, Tamura S, Kiso S, Matsumoto H, Saji Y, Yoshida Y, Fukui K, Maeda N, Nishizawa H, Nagaretani H, Okamoto Y, Kihara S, Miyagawa J, Shinomura Y, Funahashi T, Matsuzawa Y 2003 Enhanced carbon tetrachloride-induced liver fibrosis in mice lacking adiponectin. Gastroenterology 125:1796–1807
Masaki T, Chiba S, Yasuda T, Tsubone T, Kakuma T, Shimomura I, Funahashi T, Matsuzawa Y, Yoshimatsu H 2003 Peripheral, but not central, administration of adiponectin reduces visceral adiposity and upregulates the expression of uncoupling protein in agouti yellow (Ay/a) obese mice. Diabetes 52:2266–2273
Qi Y, Takahashi N, Hileman SM, Patel HR, Berg AH, Pajvani UB, Scherer PE, Ahima RS 2004 Adiponectin acts in the brain to decrease body weight. Nat Med 10:524–529
Yamauchi T, Hara K, Kubota N, Terauchi Y, Tobe K, Froguel P, Nagai R, Kadowaki T 2003 Dual roles of adiponectin/Acrp30 in vivo as an anti-diabetic and anti-atherogenic adipokine. Curr Drug Targets Immune Endocr Metabol Disord 3:243–254(Takashi Kadowaki and Tosh)