摘要
目的应用EBM-2培养犬脐血间充质干细胞(MSC),为MSC的研究提供新的细胞培养方法。方法取犬的脐血,分为四组进行细胞培养。第1组用EBM-2培养;第2组用添加有EGM-2MV的EBM-2在6孔板上培养。第3组用添加有EGM-2MV的EBM-2在纤连蛋白包被的6孔板上培养。第4组用添加有EGM-2MV的EBM-2在25cm2细胞培养瓶中培养。应用免疫组化法检测细胞抗原CD11a、CD11b、CD34、CD29及CD71的表达。结果各组均有纤维母细胞样细胞培养出。第1组细胞形态不良,增殖缓慢;第2组细胞增殖旺盛;第3组细胞克隆不稳定,容易老化;同时出现另一种细胞克隆。第4组细胞培养的结果与第3组相似。免疫组化法检测抗原显示:CD11a(-)、CD11b(-)、CD34(-)、CD29(+)、CD71(+)。结论在不用纤连蛋白包被的6孔板上,用添加有EGM-2MV的EBM-2细胞培养液可以培养出生长良好、增殖旺盛的MSC。
Objective To culture mesenchymal stem cells（MSC） in cord blood of dogs with EBM-2, providing a new method to culture cells for research in MSC. Methods Collect cord blood from dogs, and divide them into four groups. Culture the cells with EBM-2 in the first group ; with EBM-2 adding EGM-2 MV in the 6-well cell culture cluster in the second group ; with EBM-2 adding EGM-2 MV in the 6-well cell culture cluster coating with fibronectin in the third group; with EBM-2 adding EGM-2 MV in the 25 cm2 culturing flask in the fourth group. Detect antigen CDlla, CD11b, CD34, CD29 and CD71 with immunohistochemistry method. Results Fibroblast-like cells could grow up in each group. The cells grew badly in morphology and proliferated slowly in the first group, while they proli-ferated rapidly in the second group. The cell clones were instable and inclined to aging in the third group, with a new cell clone being found. The cells in the fourth group were similar to those in the third group. Surface antigens detected with immunohistochemistry method showed CD11a （ - ）, CD11b （ - ）, CD34 （ - ）, CD29 （ ＋ ）, CD71 （ ＋ ）. Conclusion The MSC could be cultured with EBM-2 adding EGM-2 MV in the 6-well cell culture cluster.
出处
《上海交通大学学报（医学版）》
CAS
CSCD
北大核心
2006年第3期259-262,共4页
Journal of Shanghai Jiao tong University:Medical Science
基金
上海市科委重点基础研究基金(01JC14027)资助项目
