实用肝脏病杂志 ›› 2011, Vol. 14 ›› Issue (2): 95-97.doi: 10.3969/j.issn.1672-5069.2011.02.003

• 论著 • 上一篇    下一篇

两种成人骨髓间充质干细胞体外分离方法的比较研究*

魏开鹏,潘兴南,王崇国   

  1. 362000 福建省泉州市 解放军第180医院南京军区肝病中心
  • 收稿日期:2010-12-02 出版日期:2011-04-10 发布日期:2016-04-15
  • 通讯作者: 潘兴南,E-mail:qz180pxn@yahoo.com.cn
  • 作者简介:魏开鹏 男,30岁,医学硕士,医师。主要从事干细胞的基础与临床研究。E-mail:kpweicn@gmail.com
  • 基金资助:
    南京军区医药卫生科研基金重点课题(编号:07Z021)

Comparative study on two methods in isolating human marrow mesenchymal stem cells in vitro

WEI Kaipeng,PAN Xingnan,WANG Chongguo   

  1. Liver Disease Center,180th Hospital,Nanjing Command of PLA, Quanzhou 362000,China
  • Received:2010-12-02 Online:2011-04-10 Published:2016-04-15

摘要: 目的 比较两种体外分离方法获得的成人骨髓间充质干细胞的形态、增殖能力和纯度。方法 分别采用直接贴壁法和密度离心法分离成人骨髓间充质干细胞,观察细胞形态;采用MTT法绘制第3代细胞的生长曲线并计算对数期倍增时间;将1×105个第3代细胞连续培养扩增至第30天并计数细胞总数;采用流式细胞仪检测第3代细胞CD31、CD34、CD73、CD105和CD166等表型。结果 两种方法获得的MMSCs均呈长梭状成纤维样细胞形态;直接贴壁法获得的细胞首次传代时间为10d,对数生长期倍增时间为30±5.6h,而密度离心法细胞首次传代时间为18d,对数生长期倍增时间为38±7.2h;连续培养至第30d时,直接贴壁法细胞总数约为密度离心法细胞的15倍;直接贴壁法第3代细胞表达CD73、CD105和CD166的阳性率均低于密度离心法(P<0.05)。结论 应用直接贴壁法和密度离心法均可有效分离成人骨髓间充质干细胞,直接贴壁法分离的细胞增殖能力更强,而密度离心法分离的细胞纯度更高。

关键词: 间充质干细胞, 骨髓, 细胞表型

Abstract: Objective To compare morphology,proliferation capacity and purity of human marrow mesenchymal stem cells by two isolation methods in vitro. Methods Human marrow mesenchymal stem cells were isolated by whole marrow culture and density gradient centrifugation. The appearance of the cells and growth curves of the third generation cells were observed. 1×105 of the third generation cells were cultured and counted continuously for 30 days. Surface antigens of the stem cells were detected with flow cytometry. Results The cells isolated by the two methods were both like long shuttle;the primary passage time of cells by whole marrow culture was 10d and the double time was 30±5.6h,while the primary passage time by density gradient centrifugation was 18d and double time was 38±7.2h;The total numbers of the former were 15 times more than the latter at 30th day. FACS showed that positive rates of CD73,CD105 and CD166 in the third generation cells isolated by whole marrow culture were less than that by density gradient centrifugation(P<0.05). Conclusion The two methods we used can successfully isolate human marrow mesenchymal stem cells. The former has a stronger proliferation ability and the latter has a higher purity of the stem cells.

Key words: Mesenchymal stem cells, Bone marrow, Cell surface