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作 者:胡琦[1] 康慧聪[1] 许峰[1] 刘晓艳[1] 王霞[1] 吴婷[1] 朱遂强[1]
机构地区:[1]华中科技大学同济医学院附属同济医院神经内科,武汉430030
出 处:《神经损伤与功能重建》2007年第6期336-339,共4页Neural Injury and Functional Reconstruction
基 金:国家自然科学基金项目(30470603;30770752)
摘 要:目的:观察携带增强型绿色荧光蛋白的2型重组腺相关病毒(rAAV2-EGFP)转导骨髓间充质干细胞(MSCs)的效率、表达时间及对细胞增殖的影响。方法:体外培养出MSCs,经传代5次、鉴定后分为2组,rAAV2组中按感染复数10。加入0.1ml rAAV2-EGFP;PBS组中加入0.1ml PBS,培养后再传代5次。用流式细胞仪检测2组P5和P10代细胞EGFP转导率,同时绘制2组P10细胞生长曲线。结果:rAAV2组P5和P10代MSCs转导率分别为21.71%±1.02%、20.34%±1.13%,差异无统计学意义(P=0.862)。生长曲线显示rAAV2组细胞生长较PBS组缓慢。结论:rAAV2-EGFP转导MSCs效率可,表达时间长,对细胞增殖稍有影响,标记后的细胞可用于观察干细胞在体内的存活、迁徙及分化。Objective: To evaluate transduction rates and expression of enhanced green fluorescent protein (EGFP) in mesenchymal stern cells (MSCs) mediated by recombinant adeno-associated virus 2 (rAAV2), and to observe impacts of the transduction on cell proliferation. Methods:MSCs were dissociated, subcultured and identified by detecting CD44,CD45,and CD90. After subculture for 5 times, the cells were divided into 2 groups, one mixed with 0. 1 ml rAAV2-EGFP with a titer of 106 , and another incubated with 0.1 ml PBS as control. After another 5 passages, transduction rates of EGFP in the P5 and P10 MSCs were detected by flow cytometry and cell growth curves were generated. Results: The transduction rates of EGFP in the P5 and P10 MSCs of rAAV2 group were 21.71%± 1.02 % and 20.34 %± 1.13% respectively, but no significant differences was found between them (P= 0. 862). The growth of MSCs in rAAV2 group was slower than that of PBS group. Conclusion: EGFP can be expressed in MSCs stably after effective transduction mediated by rAAV2. The labeled stem cells are applicable to further investigate the survival, migration and differentiation after transplantation.
分 类 号:R741[医药卫生—神经病学与精神病学]
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