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作 者:李贵新[1] 赵建强[2] 高建峰[2] 李守超[2] 李世荣[2] 路中[1] 孙秀梅[1]
机构地区:[1]潍坊医学院,山东潍坊261031 [2]潍坊市人民医院
出 处:《山东医药》2010年第19期4-6,共3页Shandong Medical Journal
基 金:山东省卫生厅青年基金项目(2005035)
摘 要:目的观察人骨髓间充质干细胞(BM-MSCs)体外扩增和定向诱导分化为神经元样细胞的变化,为其临床应用奠定基础。方法采用密度梯度离心法分离BM-MSCs细胞,用MesencultTM培养基和贴壁培养法培养、纯化和扩增细胞,流式细胞术检测细胞表面CD29和CD90分子表达率。采用20 ng/ml重组碱性成纤维细胞生长因子(bFGF)、20 ng/ml新型人表皮生长因子(hEGF)和20 g/L二甲基亚砜(DMSO)、5 mmol/Lβ-巯基乙醇(BME)分别诱导BM-MSCs;采用免疫组化法检测细胞的神经元特异性烯醇化酶(NSE)、胶原纤维酸性蛋白(GFAP)、波形蛋白(VIM)表达情况。结果BM-MSCs细胞增殖迅速,3周可传代培养;BM-MSCs传十代扩增1-2×10^3倍。分离和扩增BM-MSCs CD29、CD90强表达率分别为95.02%、93.81%。药物诱导后的BM-MSCs发生轴突等神经元样细胞变化,阳性表达NSE、GFAP、VIM分子。结论人BM-MSCs能体外培养和扩增,并能定向诱导分化为神经元样细胞。Objective To observe the proliferation of human bone marrow mesenchymal stem cells(BM-MSCs) in vitro and directional-induced differentiation into neuron-like cells,so as to provide basis for its clinical application.Methods Density gradient centrifugation was used to separate BM-MSCs,MesencultTM culture medium and pasting-wall culture method were used to culture,sublimate and proliferate BM-MSCs,CD29and CD90 clusters expressions were tested by Flow cytometry.BM-MSCs were directionally induced by 20 ng/ml human basic fibroblast growth factor(bFGF),20 ng/ml human epidermal growth factor(hEG F),20 ng/ml dimethyl sulphoxide(DMSO) and 5 mmol/L β-mercaptoethanol(BME).Immunohistochemistry was used to test the expression of neuron specific enolase(NSE),glial fibrillay acidic protein(GFAP) and vimentin(VIM).Results BM-MSCs proliferated rapidly,could be sub-cultured in 3 weeks.BM-MSCs could expand(1~2)×10^3 folds afer 10 times sub-culture.Separated and proliferated BM-MSCs expressed CD29 and CD90 clusters with the positive rate of 95.02% and 93.81% separately.The BM-MSCs occured some morphology changes included axon like structure after the induction of drugs,and the NSE,GFAP and VIM were all positively expressed in the cells.Conclusion Human BM-MSCs can be cultured and proliferated in vitro,and can differentiate into neuron like cells directionally.
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