【摘要】 目的探讨microRNA-29a(miR-29a)对大鼠心肌细胞凋亡的调控作用。方法体外培养新生SD大鼠心肌细胞,合成人miR-29a的拟似物(mimic)。用Lipofectamine RNAiMAX转染miR-29a的mimic进入心肌细胞,转染48 h后用荧光定量PCR方法检测心肌细胞miR-29a的表达变化,流式细胞仪检测细胞凋亡水平变化,Westernblot法检测凋亡相关蛋白Caspase-3和Caspase-9前体的表达变化。结果心肌细胞转染miR-29a的mimic 48 h后,心肌细胞中miR-29a的表达水平较对照组明显升高(P<0.05);心肌细胞的凋亡水平也明显升高,凋亡相关蛋白Caspase-3和Caspase-9前体的含量则明显下降(P<0.05)。结论在大鼠心肌细胞中过表达miR-29a能促进心肌细胞凋亡,其机制可能是通过Caspase-3和Caspase-9途径起作用。更多还原

【Abstract】 Aim To investigate the role of microRNA-29a(miR-29a) on apoptosis in rat cardiomyocytes. Methods In our study,newborn rats cardiomyocytes was isolated,cells were transfected with miR-29a mimic by lipofectamine RNAiMAX,and then real time RT-PCR was used to measure the level of miR-29a,flow cytometry(FCM) was used to detect the cells apoptosis,and western blot was used to detect the protein expressive level of Caspase-3 and Caspase-9. Results MiR-29a mimics could upregulate the level of miR-29a in rat cardiomyocytes after 48h of transfecting,accompanied with the increase of cells apoptosis rate,and descent of the protein level of caspase-3 and caspase-9 in cardiomyocytes when compared to the control group(P<0.05). Conclusion Our study demonstrated that the overexpression of miR-29a may regulate cells apoptosis of rat cardiomyocytes,and the mechanisms among it may be concerned with Caspase-3 and Caspase-9 pathway.更多还原