EdU体外标记人脂肪干细胞的实验研究  

Experimental study on the effect of labeling adipose derived stem cells with EdU

作　　者：张怡[1] 王克明[1] 李发成[1] 王淑杰[1] 李太颖[1] 刘新海[1] 刘美辰[1] 赵小晖 马继光[1] 

机构地区：[1]北京协和医学院中国医学科学院北京整形外科医院特需医疗部,北京100144

出　　处：《中国美容医学》2013年第1期43-47,共5页Chinese Journal of Aesthetic Medicine

摘　　要：目的:体外培养人脂肪干细胞(adi pose-deri ved st em cel l s,ADSCs)并行EdU标记,并通过测试标记率及标记后对细胞增殖分化的影响确定优化的标记时间及浓度组合。方法:使用分别采5μM,10μM,20μM,50μM的浓度及12h,24h进行标记标记ADSC,并以流式细胞仪精确测定标记率。挑选出各12h及24h时优化标记浓度,并进行标记后测定细胞活性,增殖及诱导分化实验。结果:P3代细胞约90%以上表达表面标记CD90+,CD105+,CD44+。基本不表达细胞表面标记CD45+,CD35+。通过各试验,得出最适浓度组合10μM,12h,对进一步研究脂肪干细胞在辅助脂肪移植中的作用具有指导意义。结论:EdU是标记方法简单有效,体外最佳标记浓度组合是10μM,12h。Objectives To establish the best method and optimal concentrantion and optimal time for labeling ADSC with thymidine analog,5-ethynyl-2-deoxyuridine （EdU）. Methods ADSC at passage 2-4 were labeled with EdU by diverse concentration （5μM,10μM,20μM,50μM）and diverse time （12h,24h）.After labeled, the cell were stained by ALEXA-555 analyzed by fluorescence microscopy and flow cytometer.The impact of EdU on the growth of ADSCs was examined by trypan blue exclusion,methylthiazoly tetrazoliμM （MTT） assay and assess multiple differentiation potential of ADSC using in vitro osteogenic and adipogenic induction. Results Labeling with EdU in vitro can be easily performed,And labeling stem cells with the concentration of 10μM with 12h is the optimal concentration and time. The optimal concentration andtime of labeling has little impact on the growth of ADSC or on the differentiation and can therefore be used for ADSC trading. Conclusion The lebeling method with EdU is simple but efficacious,and the optimal group is labeling with the concentration of 10μM and the time with 12h.

关 键 词：脂肪干细胞 细胞治疗 EDU 干细胞标记 细胞示踪 

分 类 号：R622[医药卫生—整形外科] Q813.1[医药卫生—外科学]