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中国应用生理学杂志 ›› 2017, Vol. 33 ›› Issue (6): 514-518.doi: 10.12047/j.cjap.5601.2017.122

• 研究论文 • 上一篇    下一篇

miR-148a在5-aza诱导间充质干细胞心肌样分化中的调控作用及机制

蒋昌科, 龚放   

  1. 重庆医科大学附属永川医院儿科, 重庆 402160
  • 收稿日期:2017-02-24 修回日期:2017-10-17 出版日期:2017-11-28 发布日期:2018-06-19
  • 基金资助:
    2015年重庆市基础与前沿研究计划项目(cstc2015jcyjA10042);2015年重庆市永川区自然科学基金计划项目(Ycstc,2015nc5003)

Regulation and mechanism of miR-148a on cardiomyocyte differentiation induced by 5-aza in mesenchymal stem cells

JIANG Chang-ke, GONG Fang   

  1. Department of Pediatrics, Yongchuan Hospital Affiliated to Chongqing Medical University, Chongqing 402160, China
  • Received:2017-02-24 Revised:2017-10-17 Online:2017-11-28 Published:2018-06-19
  • Contact: 蒋昌科,Tel:023-85382120;E-mail:943099372@qq.com E-mail:943099372@qq.com
  • Supported by:
    2015年重庆市基础与前沿研究计划项目(cstc2015jcyjA10042);2015年重庆市永川区自然科学基金计划项目(Ycstc,2015nc5003)

摘要: 目的:探讨miR-148a在5-aza诱导人骨髓间充质(hMSCs)成心肌样分化中的表达及miR-148a对hMSCs体外成心肌样分化的生物学作用。方法:免疫荧光检测5-aza诱导hMSCs分化后心肌细胞特异性标志物α-MHC表达水平;qRT-PCR和Western blot分别检测miR-148a和DNMT1在hMSCs成肌样分化中的表达水平。利用Lipofectamine TM 2000将miR-148a mimics和miR-148a inhibitor分别瞬时转染hMSCs,Western blot检测心肌细胞特异性标志物α-MHC的蛋白表达水平。利用生物信息学技术预测miR-148a的靶基因结合位点利用双荧光素酶报告基因系统鉴定其对靶基因3'UTR的结合序列。通过DNMT1 shRNA和miR-148a inhibitors共转到hMSCs中,研究miR-148a在hMSCs成心肌样分化中的调控作用。结果:hMSCs经5-aza诱导分化后,心肌细胞特性标志物α-MHC蛋白水平明显上调。miR-148a在hBMSCs成肌样分化中显著性增加(P<0.01),DNMT1表达水平显著降低。过表达miR-148a能提高hBMSC中心肌细胞特异性标志物α-MHC表达水平,而抑制miR-148a则能降低其水平(P<0.01)。DNMT1沉默可以阻断miR-148a对hMSCs的诱导成肌样分化作用。结论:miR-148a在hMCCs成肌样分化中表达上调,通过靶定和调控DNMT1基因的表达,并对hMSCs心肌向分化具有正向调控作用。

关键词: miR-148a, 骨髓间充质, 心肌样分化, DNMT1

Abstract: Objective: To investigate the expression of miR-148a in the process of myocardial differentiation of human mesenchymal stem cells (hMSCs) induced by 5-azacytidine (5-aza) and study the effects of miR-148a on myocardial differentiation of hMSCs.Methods: The immunofluorescence analysis was used to detect the expressions of the associated mark genes of cardiac specific protein (α-MHC) in the process of myocardial differentiation of hMSCs induced by 5-aza. qRT-PCR and Western blot were used to analysis the expressions of miR-148a and DNA methyltransferase 1 (DNMT1) after myocardial differentiation of hMSCs, respectively. The expression of α-MHC after transfection with synthetic miR-148 mimics and miR-148a inhibitor was examined by Western blot. We used bioinformatics analysis to predict the potential target of miR-148a, and the dual luciferase report gene system was used to verify the predication. After co-transfected with DNMT1 shRNA and miR-148a inhibitors, hMSCs were used to explore the regulatory role and mechnism of miR-148a in the process of myocardial differentiation of hMSCs.Results: α-MHC was increased significantly after induced by 5-azacytidine. miR-148a was increased significantly in cardiomyocyte differentiation of hMSCs, while the gene and protein expression levels of DNMT1 were decreased significantly in this progress (P<0.01). The expression of α-MHC was up-regulated significantly in hMSCs when miR-148a was induced into cardiomyocyte differentiation and overexpressed. Instead, downregulation of miR-148a suppressed α-MHC expression (P<0.01). Knockdown of DNMT1 blocked the role of miR-148a in differentiation of hMSCs.Conclusion: miR-148a was upregulated in cardiomyocyte differentiation of hMSCs, and miR-148a promoted myocardial differentiation of hMSCs via targeting DNMT1.

Key words: miR-148a, mesenchymal stem cells, cardiac differentiation, DMNT1

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