基础医学与临床 ›› 2015, Vol. 35 ›› Issue (3): 295-302.

• 研究论文 • 上一篇    下一篇

表达HIF1αmu EPCs增强BMP2转染BMSCs成骨及成血管能力

於绍龙1,刘丹平2,赵辉1,齐鑫1,张解元1,李谌1   

  1. 1. 辽宁医学院
    2. 辽宁医学院附属第一医院
  • 收稿日期:2014-08-14 修回日期:2014-12-01 出版日期:2015-03-05 发布日期:2015-03-03
  • 通讯作者: 刘丹平 E-mail:291314442@qq.com
  • 基金资助:
    衰老调控因子SIRT6与NF-κB对话在人参皂苷Rg1延缓造血干/祖细胞衰老中的作用;辽宁省卫生厅“百千万人才工程”

EPCs expressing hypoxia inducible factor 1αmu enhanced osteogenesis and angiogenesis of BMSCs transfected with bone morphogenetic protein 2

  • Received:2014-08-14 Revised:2014-12-01 Online:2015-03-05 Published:2015-03-03

摘要: 目的 研究表达突变型低氧诱导因子1α的内皮祖细胞 (EPCs) 对骨形成蛋白2(BMP2)转染的骨髓基质细胞(BMSCs)成骨及成血管的影响。方法 密度梯度离心法分离培养兔BMSCs和EPCs并鉴定,MTT法检测不同比例BMSCs/EPCs混合培养时增殖作用,以确定混合细胞比例。实验分为6组:A组(BMSCs) ;B组(Adv-BMP2-BMSCs);C组(BMSCs+EPCs);D组(Adv-BMP2-BMSCs+EPCs);E组(BMSCs+Adv-HIF1αmu-EPCs);F组(Adv-BMP2-BMSCs+Adv-HIF1αmu-EPCs)。以Adv-HIF1αmu和Adv-BMP2的最佳转染指数 (MOI) 分别转染EPCs和BMSCs。Western blot检测HIF-1α和BMP-2蛋白表达。行碱性磷酸酶活性检测;用qRT-PCR检测相关基因的表达,以评价共培养细胞成骨和成血管情况。结果 BMSCs与EPCs以1:1混合培养增殖能力优于1:2及2:1,故该实验混合细胞比例确定为1:1。Adv-BMP2-BMSCs和BMSCs组可见BMP-2蛋白表达且表达量高于EPCs和Adv-HIF1αmu-EPCs 组(P< 0.05)。Adv-HIF1αmu-EPCs组可见HIF1α蛋白表达且表达量明显高于Adv-BMP2-BMSCs、BMSCs及EPCs组(P< 0.05)。F组ALP活性以及成骨和成血管相关基因表达高于其他组(P<0.05)。结论 表达HIF1αmu的EPCs能够增强Adv-BMP2-BMSCs成骨和成血管潜能。

关键词: 突变型低氧诱导因子1α, 内皮祖细胞, 骨形态发生蛋白2, 骨髓基质细胞, 成骨, 成血管

Abstract: Objective To study the effect of endothelial progenitor cells (EPCs) expressing hypoxia inducible factor 1αmu on osteogenesis and angiogenesis of bone morphogenetic protein 2 transfected bone marrow stromal cells(BMSCs) .Methods BMSCs and EPCs were obtained and identified from rabbit bone marrow by density gradient centrifugation.To define the best ratio of EPCs and BMSCs,MTT assay was used to detect the proliferation of different proportion of BMSCs/EPCs.Experiment was divided into 6 groups according to different cells and genes transfected:group A:BMSCs ;group B:Adv-BMP2-BMSCs;group C:BMSCs plus EPCs;group D:Adv-BMP2-BMSCs plus EPCs;group E:BMSCs plus Adv-HIF1αmu-EPCs;group F:Adv-BMP2-BMSCs plus Adv-HIF1αmu-EPCs. Adv-HIF1αmu and Adv-BMP2 were respectively transfected into EPCs and BMSCs with the optimum multiplicity of infection (MOI).The expressions of BMP2 and HIF-1α proteins were detected by Western blot .The osteogenesis and angiogenesis potential of co-cultured cells were detected by alkaline phosphatase (ALP) activity and qRT-PCR.Result The co-culture proportion of BMSCs and EPCs was 1:1.Western blot showed that expression of BMP2 protein in groups of Adv-BMP2-BMSCs、BMSCs was higher than that in the groups of Adv-HIF1αmu EPCs and EPCs(P<0.05),expression of HIF-1α protein in group of Adv-HIF1αmuEPCs was higher than that in the groups of Adv-BMP2 -BMSCs、BMSCs and EPCs(P<0.05).Alkaline phosphatase activity and osteogenesis and angiogenesis related gene expression in group F were higher than that in other groups (P<0.05).Conclusion Adv-HIF1αmu EPCs co-cultured with Adv-BMP2 -BMSCs can promote osteogenesis and angiogenesis of Adv-BMP2-BMSCs.

Key words: mutant hypoxia inducible factor1α, endothelial progenitor cells, morphogenetic protein 2, Bone marrow stromal cells, Osteogenesis, Angiogenesis