人骨髓间质干细胞分离和培养扩增方法的研究
骨髓间质干细胞,,骨髓间质干细胞;,分离扩增,1材料与方法,2结果,3讨论,参考文献
摘 要 目的:探索分离、纯化及培养成人骨髓间质干细胞(hMSC)的最佳方法。方法:采用FicollPaque淋巴细胞分离液和全血接种两种方法分离成人MSC,筛选体外培养hMSC适合的培养基和适宜的血清含量,流式细胞仪检测hMSC表面抗原表达。结果:经FicollPaque淋巴细胞分离液分离后,接种于φ=100 mL/L胎牛血清的LDMEM培养液,细胞贴壁良好,增殖速度快,hMSC在体外扩增5代可获得1×108细胞。全血接种分离hMSC,细胞贴壁慢、少,生长情况欠佳。除LDMEM,其他类型的培养基均不适合hMSC的培养扩增。流式细胞仪检测结果显示CD29、CD44、CD105、CD166表达阳性,CD14、CD33、CD34、CD38、CD45、CD11a为阴性。结论:用FicollPaque淋巴细胞分离液分离骨髓单核细胞,接种于φ=100 mL/L FCS的LDMEM培养液,分离培养扩增hMSC的效果最好。关键词 骨髓间质干细胞; 分离扩增
Study on isolation and cultivation of mesenchymal stem cells from human bone marrow
Abstract Objective: To establish a method for isolation and cultivation of mesenchymal stem cells (MSCs) from human bone marrow. Methods: hMSCs were separated from human marrow with FicollPaque reagent or direct culture and expanded in different culture medium with newborn bovine serum. The proliferation and growth characteristics were observed in primary and passage culture. To detect the surface antigens, the labeled cells were analysed on a FACScan flow cytometer. Results: The isolated hMSCs comprised a single phenotypic population and displayed a fibroblastlike morphology. hMSCs had a strong selfrenewal capacity. After P5 culture,1×108 cells were obtained. LDMEM was better for the proliferation and growth of MSC. These expanded attached MSCs were uniformly positive for CD29、CD44、CD105、CD166,without the expression of CD11a、CD14、CD33、CD34、CD45、CD38. Conclusion: MSCs can be satisfactorily isolated from human marrow with FicollPaque reagent and expanded in LDMEM culture medium. ......
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