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桑甜甜 曹青 王飞 黄黎亚 王玉强 陈书艳 刘芳 张建军.FOXO3a过表达对内皮祖细胞周期相关蛋白的调控[J].现代生物医学进展英文版,2014,14(24):4626-4629.
FOXO3a过表达对内皮祖细胞周期相关蛋白的调控
The Effects of FOXO3a Overexpression on the Cell Cycle RegulatoryProteins in Endothelial Progenitor Cells
  
DOI:
中文关键词: 内皮祖细胞  腺病毒载体  细胞增殖
英文关键词: Endothelial progenitor cells  Adenovirus vector  Cell proliferation
基金项目:国家自然科学基金项目(30973152,8 1270205)
Author NameAffiliation
SANG Tian-tian, CAO Qing, WANG Fei, HUANG Li-ya, WANG Yu-qing, CHEN Shu-yan, LIU Fang, ZHANG Jian-jun 上海交通大学医学院附属新华医院老年医学科上海市浦东新区公利医院心内科 
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中文摘要:
      目的:观察FOXO3a(forkhead box O3a)的活性改变对内皮祖细胞(endothelial progenitor cells,EPCs)增殖和细胞周期相关蛋 白表达的影响。方法:将携带突变激活FOXO3a 基因的腺病毒载体Ad-TM (triple mutant)-FOXO3a 和阴性对照腺病毒载体 Ad-GFP 体外感染人脐血来源的EPCs。观察EPCs形态学改变,CCK-8 分析转染后EPCs增殖情况,Western blot检测FOXO3a 蛋 白、细胞周期相关蛋白p27kip1以及CDK2 的表达水平。结果:构建了的2 种腺病毒相关载体被成功转染。形态学改变方面, Ad-TM-FOXO3a 组EPCs细胞生长缓慢,集落不明显;Western blot 和CCK-8 结果显示,Ad-TM-FOXO3a 转染组与阴性对照组相 比,EPCs 增殖被抑制,FOXO3a 与p27kip1蛋白过表达,CDK2 表达下调。结论:FOXO3a 可能通过上调p27kip1 蛋白表达,下调 CDK2 表达,以抑制EPCs增殖。
英文摘要:
      Objective:To investigate the effects of FOXO3a overexpression on the proliferation of endothelial progenitor cells (EPCs) and the expression of the cell cycle regulatory proteins.Methods:Two constructed recombinant adenovirus vectors, Ad-TM (triple mutant)-FOXO3a and the control Ad-GFP, were transfected into EPCs from human cord blood in vitro. The changes in cell morphology and proliferation of transfected EPCs were detected by fluorescent microscope and CCK-8 assay, respectively. The protein expression changes of FOXO3a, cell cycle regulatory proteins p27kip1 and CDK2 were assessed by Western blot.Results:The both recombinant adenovirus vectors were successfully transfected into EPCs. The results demonstrated that compared with control group, in the Ad-TM-FOXO3a group had the overexpressed-FOXO3a, while cell division proceeded slowly and proliferation EPCs was significantly inhibited; Meanwhile p27kip1 were upregulated while CDK2 expression was downregulated.Conclusion:FOXO3a may inhibit proliferation of EPCs via up-regulating the expression of p27kip1 and down-regulating the expression of CDK2.
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