文章摘要
张鹭鹭刘惊今王永顺刘芳于波△.microRNA499 慢病毒载体转染诱导大鼠骨髓间充质干细胞 向心肌样细胞分化*[J].,2012,12(26):5027-2031
microRNA499 慢病毒载体转染诱导大鼠骨髓间充质干细胞 向心肌样细胞分化*
miR-499 Induces Cardiac Differentiation of Rat Bone Marrow-DerivedMesenchymal Stem Cells*
  
DOI:
中文关键词: microRNA 499  骨髓间充质干细胞  心肌样分化  慢病毒载体转染
英文关键词: miR-499  Mesenchymal stem cells  Cardiac differentiation  Lentiviral vectors transfection
基金项目:省部共建教育部重点实验室(哈尔滨医科大学)开放基金项目(KF201004)
作者单位
张鹭鹭刘惊今王永顺刘芳于波△ 哈尔滨医科大学附属第二医院心内科心肌缺血机理与诊疗技术省部共建教育部重点实验室(哈尔滨医科大学) 
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中文摘要:
      目的:探讨microRNA 499( miR-499)慢病毒转染对诱导大鼠骨髓来源间充质干细胞(BM-MSCs)向心肌样细胞分化的作用。 方法:取第四代Wistar大鼠骨髓来源间充质干细胞进行流式细胞检测,鉴定干细胞表面特异标记物。使用符合干细胞鉴定标准的 细胞批次用于后续实验。实验设置miR499慢病毒转染、慢病毒空白转染2个处理组,分别于处理后即日、1d,3d,5d,7d 收集细胞 进行下列实验:实时荧光定量PCR 检测心肌重要转录因子GATA4、NKx2.5 和MEF2C 的mRNA 表达, western-blot 检测心肌特 异蛋白I( cTnI)的表达。结果:培养第四代Wistar大鼠骨髓来源间充质干细胞表达干细胞表面特异标记物,可用于实验。大鼠骨髓 来源间充质干细胞microRNA 499慢病毒载体转染后microRNA 499 表达明显升高,且转染后1d,3d,5d,7d, GATA4、NKx2.5 和 MEF2C的mRNA表达逐渐增强。慢病毒空白转染组未见明显变化。western-blot检测自第3天开始可见cTnI阳性表达条带,慢病 毒空白转染组未检测到明显阳性表达条带。结论:microRNA 499可诱导大鼠骨髓来源间充质干细胞向心肌样细胞分化。
英文摘要:
      Objective: To investigate the effect of miR-499 on differentiation of cardiomyocyte-like cells from rat bone marrow-derived mesenchymal stem cells (BM-MSCs). Methods: The fourth passage of rat BM-MSCs were infected with lentiviral vectors bearing miR-499 or empty lentiviral vectors as control. The expression of cardiac-specific markers, NKx2.5, GATA4, MEF2C, and cTnI in these cells were examined by real-time PCR and western blot. Results: The fourth passage of the cultured rat BM-MSCs express significant markers of MSCs. After transfection of microRNA 499 in rat BM-MSCs, the expression level of microRNA 499 was markedly enhanced. The mRNA expression of GATA4, NKx2.5 and MEF2C gradually increased from day 1 to day 7, the cTnI expression was detected from day 3. While there were no significant changes of GATA4, NKx2.5 and MEF2C mRNA levels in BM-MSCs infected with empty lentiviral vectors, and cTnI expression cannot be detected either. Conclusion: Over-expression of miR-499 rat BM-MSCs can induce rat BM-MSCs toward cardiac differentiation.
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