BMSCs的分离培养、纯化与鉴定

目的 建立一种持续、稳定的可多向分化的骨髓间充质干细胞(BMSCs)体外分离培养体系.方法 运用密度梯度离心法从1月龄新西兰兔骨髓中分离培养BMSCs,利用相差显微镜观察其形态及生长情况,扫描电镜观察其细胞结构,运用流式细胞术分析分离细胞群所处细胞周期和细胞活力,用MTT比色法绘制细胞生长曲线,并用特定诱导液将分离的BMSCs向成骨细胞和成脂肪细胞定向诱导分化,利用ALP和油红O进行染色鉴定.结果 所分离的BMSCs细胞在形态学观察与生长动力学上均符合BMSCs特征,分离培养的BMSCs细胞在第3天进入对数生长期,第10天进入平台期;在成骨、成脂肪的诱导培养条件下,分别出现成骨、成脂肪表型特征,可进一步定向分化,结论所收获的细胞具有BMSCs的特异性.

Bone marrow-derived mesenchymal stem cells isolation, culture and identification

Objective To establish a sustained and stable bone marrow-derived mesenchymal stem cells (BMSCs) isolation and culture system which could be pluripotential in vitro. Methods BMSCs were isolated and cultured from the 1-month-old New Zealand white rabbits through density-gradient centrifugation. Growth and ultromicrostructure of the BMSCs were observed by light-microscope and scan electron-microscope. The cell activities and cell cycle were observed by flow cytometry. The grow curve of the BMSCs was described through MTT assay. BMSCs were induced and differentiate into osteoblasts and adipocytes by specific induction culture medium. Then the cells were stained with alkaline phosphatase (ALP) and Oil red O , and analyzed the result of all staining. Results The isolated BMSCs cells were in line with the characteristics of BMSCs in morphology and growth kinetics, and the isolated BMSCs cells would be into the logarithmic growth phase in the third day and into the platform phase in the tenth day. Conclusions In the osteogenic and adipogenic-induced culture conditions, BMSCs have appeared the phenotypic characteristics of osteogenic and adipogenic respectively, and could be further directed differentiation. These indicated the harvested cells possessed BMSCs specificity.