Mitochondria sensitive to ER Ca2+ stores
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《细胞学杂志》
The endoplasmic reticulum (ER) converses with mitochondria during apoptosis, as reported on page 1115. The article by Breckenridge et al. identifies Ca21 as an interorganellar signal that sensitizes mitochondria to death-inducing injuries.
The link between ER-associated events and mitochondrial remodeling during cell death lies in the BAP31 protein, an integral ER membrane protein that is a target of caspase-8. Previous studies indicated that full-length BAP31 inhibits mitochondrial release of cyt c during apoptosis, whereas overexpression of BAP31's caspase cleavage product, p20, induces cell death. The current study demonstrates that p20 exerts its apoptosis-inducing activity from the ER by inducing mitochondrial fission.
ER and mitochondria were found to communicate through an exchange of Ca2+. Expression of p20 induced Ca2+ release from the ER and near simultaneous Ca2+ uptake into the mitochondria. The high mitochondrial Ca2+ levels recruited a dynamin- related protein called Drp1, which is known to effect fission. The resulting fragmentation sensitized mitochondria to downstream caspase-8 activities that cause cyt c release. Compared with caspase-8 action alone, the addition of p20 increased cyt c release several fold in vivo. Although isolated mitochondria readily release cyt c in response to caspase signals alone, mitochondria in intact cells may have structural differences that require priming by Drp1 for efficient release of cyt c.(Cleavage of BAP31 causes mitochondria (r)
The link between ER-associated events and mitochondrial remodeling during cell death lies in the BAP31 protein, an integral ER membrane protein that is a target of caspase-8. Previous studies indicated that full-length BAP31 inhibits mitochondrial release of cyt c during apoptosis, whereas overexpression of BAP31's caspase cleavage product, p20, induces cell death. The current study demonstrates that p20 exerts its apoptosis-inducing activity from the ER by inducing mitochondrial fission.
ER and mitochondria were found to communicate through an exchange of Ca2+. Expression of p20 induced Ca2+ release from the ER and near simultaneous Ca2+ uptake into the mitochondria. The high mitochondrial Ca2+ levels recruited a dynamin- related protein called Drp1, which is known to effect fission. The resulting fragmentation sensitized mitochondria to downstream caspase-8 activities that cause cyt c release. Compared with caspase-8 action alone, the addition of p20 increased cyt c release several fold in vivo. Although isolated mitochondria readily release cyt c in response to caspase signals alone, mitochondria in intact cells may have structural differences that require priming by Drp1 for efficient release of cyt c.(Cleavage of BAP31 causes mitochondria (r)