首页 | 本学科首页   官方微博 | 高级检索  
     

成人骨髓间充质干细胞分化为血管内皮细胞的研究
引用本文:晏开力,汪健,李庆,邬志伟,徐修才,徐静玮,翟志敏. 成人骨髓间充质干细胞分化为血管内皮细胞的研究[J]. 中国修复重建外科杂志, 2007, 21(1): 76-80
作者姓名:晏开力  汪健  李庆  邬志伟  徐修才  徐静玮  翟志敏
作者单位:安徽省立医院中心实验室,合肥,230000
基金项目:安徽省教育厅自然科学基金
摘    要:目的研究成人骨髓间充质干细胞(marrow mesenchymal stem cells,MSCs)体外分化为血管内皮细胞的能力并探讨其诱导条件。方法分离成人骨髓单个核细胞,经贴壁法获取MSCs。所获细胞分4组进行诱导:组1、2以5×10^3/cm^2细胞密度接分别接种于含2%和15%胎牛血清的L—DMEM培养基;组3、4以5×10^4/cm^2细胞密度分别接种于上述两种血清浓度的培养基,各组细胞经血管内皮生长因子(vascular endothelial growth factor,VEGF)辅以牛脑提取物的诱导,对照组为正常传代培养的MSCs。在诱导的第14、21天分别测定表面分子CD34、VEGFR-2、CD31和Ⅶ因子相关抗原(factor Ⅷ—related antigen,又称von Willebrand factor,vWF)以及体外成血管实验对分化细胞进行鉴定,同时测定不同诱导条件下的细胞增殖指数(proliferation index,PI)。结果组3细胞经诱导后,内皮系表面分子CD34、VEGFR-2、CD31、vWF于第14天均有不同程度表达,分别为8.5%、12.0%、40.0%、30.0%.其中CD34、VEGFR-2在第21天表达上调,为15.5%、20.0%,余各诱导组细胞未表达上述表面分子;诱导后的组3细胞呈低增殖状态(PI值约为10.4%),在半固体培养基中还可形成血管腔样结构。结论从成人骨髓中分离培养的MSCs,在较高细胞接种密度和低增殖状态下,经VEGF、牛脑垂体提取物诱导后,可分化为血管内皮细胞,可作为治疗性血管生成及组织工程理想的种子细胞。

关 键 词:骨髓间充质干细胞  分化  血管内皮细胞  体外培养
修稿时间:2005-07-01

EXPERIMENTAL STUDY ON DIFFERENTIATION OF ADULT MARROW MESENCHYMAL STEM CELLS INTO VASCULAR ENDOTHELIAL CELLS IN VITRO
YAN Kaili, WANG Jian, LI Qing,et al.. EXPERIMENTAL STUDY ON DIFFERENTIATION OF ADULT MARROW MESENCHYMAL STEM CELLS INTO VASCULAR ENDOTHELIAL CELLS IN VITRO[J]. Chinese journal of reparative and reconstructive surgery, 2007, 21(1): 76-80
Authors:YAN Kaili   WANG Jian   LI Qing  et al.
Affiliation:Department of Central Experimental Laboratory, Anhui Provincial Hospital, Hefei Anhui, 230000, P. R. China
Abstract:OBJECTIVE: To study the differenation of adult marrow mesenchymal stem cells (MSCs) into vascular endothelial cells in vitro and to explore inducing conditions. METHODS: MSCs were isolated from adult marrow mononuclear cells by attaching growth. MSCs were divided into 4 groups to induce: the cells seeded at a density of 5 x 10(3)/cm(2) in 2% and 15% FCS L-DMEM respectively (group 1 and group 2), at a density of 5 x 10(4)/cm2 in 2% and 15% FCS L-DMEM respectively (group 3 and group 4); vascular endothelial growth factor (VEGF) supplemented with Bovine pituitary extract was used to induce the cell differentiation. The differentiated cells were identified by measuring surface marks (CD34, VEGFR-2, CD31 and vWF ) on the 14th day and 21st day and performed angiogenesis in vitro on the 21st day. The cell proliferation index (PI) of different inducing conditions were measured. RESULTS: After induced in VEGF supplemented with Bovine pituitary extract, the cells of group 3 expressed the surface marks CD34, VEGFR-2, CD31 and vWF on the 14th day, the positive rates were 8.5%, 12.0%, 40.0% and 30.0% respectively, and on the 21st day the positive rates of CD34 and VEGFR-2 increased to 15.5% and 20.0%, while the other groups did not express these marks; the induced cells of group 3 showed low proliferating state (PI was 10.4%) and formed capillary-like structure in semisolid medium. CONCLUSION: Adult MSCs can differentiate into vascular endothelial cells after induced by VEGF and Bovine pituitary extract at high cell densities and low proliferating conditions, suggesting that adult MSCs will be ideal seed cells for the therapeutic neovascularization and tissue engineering.
Keywords:Marrow mesenchymal stem cells Differentiation Vascular endothelial cells Culture in vitro
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号