Isolation and culture of bone marrow mesenchymal stem cells from human fetus and their biological properties

Zhang Yihua, Dou Zhong-ying, Shen Wen-zheng, Yang Chun-rong, Gao Zhimin
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引用次数: 6

Abstract

The population doubling number(70~80 times) of human fetal bone marrow mesenchymal stem cells(BMMSCs) is about two times more than that (30~40 times) of the adult BMMSCs, and their differentiation capacity is superior to that of their adult counterparts. In this study, BMMSCs were isolated from 2- to 3-month-old human abortuses by scissoring their long bones lengthwise, followed by rinsing and culturing whole marrow cells. Basic medium and serum concentration for BMMSCs culture were optimized and growth curves made, both with MTT(3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di-phenytetrazoliumromide) reduction assay. Isolated cells were identified with flow-cytometry and immunocytochemistry for their antigen markers. The biosafety of isolated cells was evaluated by karyotype analysis and tumor forming experiment. The results indicated that lengthwise scissoring of fetal long bones and rinsing of their marrow cells was practical and useful to obtain the BMMSCs from human abortuses at the age of 2~3 months. In this experiment, α-MEM(minimum essential medium alpha medium) +20% FCS(fetal cattle serum) was the best system for the BMMSCs in vitro. The third passage BMMSCs expressed Oct4, SSEA3 and SSEA4 beside the surface markers of their adult counterparts. The population doubling time of the BMMSCs of passage 6, 12 and 24 were 34,36 and 40 h, respectively. The cells in all the passages showed diploid karyotype and formed no tumor in the nude mice. The BMMSCs of human abortuses at the age of 2~3 months were proved to be biologically safe and ideal seed cells for researches on human tissue engineering and regeneration medicine.
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人胎骨髓间充质干细胞的分离培养及其生物学特性研究
人胎儿骨髓间充质干细胞(BMMSCs)的群体倍增数(70~80倍)是成人骨髓间充质干细胞(30~40倍)的2倍左右,分化能力优于成人骨髓间充质干细胞。在这项研究中,从2至3个月大的流产患者中,通过纵向剪断其长骨,然后冲洗和培养整个骨髓细胞,分离出骨髓间充质干细胞。采用MTT(3-(4,5)-二甲基噻吩偶氮(-z-y1)-3,5-二苯四氮唑胺)还原法,优化BMMSCs培养的基本培养基和血清浓度,并绘制生长曲线。用流式细胞术和免疫细胞化学对分离细胞进行抗原标记鉴定。通过核型分析和肿瘤形成实验评价分离细胞的生物安全性。结果表明,将胎儿长骨纵向剪断并冲洗其骨髓细胞可获得2~3月龄人流产骨髓间充质干细胞。在本实验中,α-MEM(minimum essential medium - α medium) +20%胎牛血清是体外培养BMMSCs的最佳体系。第三代BMMSCs表达Oct4、SSEA3和SSEA4,并在其成体对应物的表面标记旁表达。传代6、12和24的BMMSCs群体倍增时间分别为34、36和40 h。所有传代细胞的核型均为二倍体,未在裸鼠体内形成肿瘤。2~3月龄人流产骨髓间充质干细胞具有良好的生物学安全性,是开展人体组织工程和再生医学研究的理想种子细胞。
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