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脐带间充质干细胞在不同培养体系条件下的生物学特性
作者姓名:周建宇  徐 悦  黄文敬  刘俊江  洪敬欣
作者单位:协和干细胞基因工程有限公司,天津市 300384
摘    要:背景:体外培养的脐带间充质干细胞在不同培养体系下生长状态差异显著,因此选取一种更适合的培养基相当必要。 目的:对比观察人脐带间充质干细胞在3种培养基中的生长增殖情况,并检测细胞免疫表型以及间充质干细胞的诱导分化能力。 方法:在无菌条件下用贴块法收获人脐带间充质干细胞,用T75培养瓶培养传代后,取第3代脐带间充质干细胞分别种入到含体积分数为5%胎牛血清的DMEM/F12培养基、含体积分数为10%胎牛血清的DMEM/F12培养基和Mesen PRO RSTM培养基中,培养第1,3,5,7天进行细胞计数,绘制细胞生长曲线。采用流式细胞仪分析第3代脐带间充质干细胞免疫表型,并检测其成骨及成脂肪诱导分化能力。 结果与结论:培养出的第3代人脐带间充质干细胞高表达CD44、CD73、CD90、CD105,不表达CD29、CD31、CD34、HLA-DR。经成脂诱导后,油红O染色可见胞浆中有大量红色小脂滴;成骨诱导后,茜素红染色后镜下可见成骨样细胞团,说明脐带间充质干细胞在体外具有多向分化的潜能。在倒置显微镜下观察可见含体积分数为10%胎牛血清的DMEM/F12培养基中的细胞集落密集,形态均匀,而其他2种培养基中的细胞集落密集程度和形态都不如前者好。在培养传代细胞时,可优先选择含体积分数为10%胎牛血清的DMEM/F12培养基。中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程全文链接:

关 键 词:干细胞  脐带脐血干细胞  培养基  脐带间充质干细胞  诱导分化  
收稿时间:2014-07-14

Biological characteristics of umbilical cord mesenchymal stem cells in different conditioned media
Authors:Zhou Jian-yu  Xu Yue  Huang Wen-jing  Liu Jun-jiang  Hong Jing-xin
Institution:Union Stemcell & Gene Engineering Co., Ltd., Tianjin 300384, China
Abstract:BACKGROUND:The growth of mesenchymal stem cells in vitro in different conditioned media is different evidently. So it is necessary to choose a more suitable medium. OBJECTIVE:To contrast and observe the proliferation of human umbilical cord mesenchymal stem cells in three kinds of media and to check the immunophenotype and differentiation ability of mesenchymal stem cells. METHODS: Human umbilical cord mesenchymal stem cells were collected by explant method in sterile conditions. After subculturing by T75 incubation bottles, the third generation of mesenchymal stem cells were cultured in Dulbecco’s modified Eagle’s medium/Ham’s nutrient mixture F-12 medium containing 5% fetal bovine serum, Dulbecco’s modified Eagle’s medium/Ham’s nutrient mixture F-12 containing 10% fetal bovine serum and Mesen PRO RSTM medium. After 1, 3, 5, 7 days of culture, the cells were counted to draw a growth curve. Immunophenotype of the third generation of umbilical cord mesenchymal stem cells were determined by flow cytometry and the ability of osteogenic and adipogenic differentiation was also detected. RESULTS AND CONCLUSION: The third generation of cells cultured highly expressed CD44, CD73, CD90, CD105, but did not express CD29, CD31, CD34, HLA-DR. The oil red O staining showed a lot of little red lipid drops after adipogenic induction; alizarin red staining showed osteoblast-like cells after osteogenic induction, indicating umbilical cord mesenchymal stem cells in vitro have the potential of multi-directional differentiation. After observation and counting, the colony and shape of cells cultured in Dulbecco’s modified Eagle’s medium/Ham’s nutrient mixture F-12 containing 10% fetal bovine serum were superior to those cultured in the other two media. Therefore, it is concluded that Dulbecco’s modified Eagle’s medium/Ham’s nutrient mixture F-12 containing 10% fetal bovine serum is preferred for cell subculture.
Keywords:stem cells  umbilical cord  mesenchymal stem cells  culture media  
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