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作 者:范玉璟[1] 廖华[1] 陈光慧[2] 郭小梅[1]
机构地区:[1]华中科技大学附属同济医院心内科,武汉430030 [2]美国国立卫生研究所心血管研究室
出 处:《临床心血管病杂志》2012年第9期714-717,共4页Journal of Clinical Cardiology
基 金:国家自然科学基金资助项目(No:30872714)
摘 要:目的:研究线粒体融合素基因2(Mfn2)的突变体片段Mfn2-1A,对自发性高血压大鼠血管平滑肌细胞的增殖抑制作用,并进一步探讨相关作用机制。方法:用已构建的重组腺病毒Adv-Mfn2-1A感染大鼠血管平滑肌细胞,利用细胞计数、四甲基偶氮唑盐比色法检测血管平滑肌细胞增殖,流式细胞仪检测细胞生长周期,蛋白免疫印迹法分析Mfn2-1A对信号通路Mek-Erk1/2蛋白表达水平的影响。结果:重组腺病毒Adv-Mfn2-1A感染平滑肌细胞能正常表达相应蛋白;转染Adv-Mfn2-1A后能抑制平滑肌细胞增殖(P<0.05),第3天开始效果明显;Adv-Mfn2-1A较Adv-Mfn2作用效果更显著(P<0.05);转染Adv-Mfn2-1A和Adv-Mfn2后阻滞于G0/G1期的细胞明显增多,转染Mfn2-1A后阻滞在G0/G1期细胞达到(77.74±3.67)%;Mfn2-1A可降低平滑肌细胞中磷酸化Erk1/2蛋白的表达,效果比Mfn2更明显(P<0.05)。结论:Mfn2基因突变体片段1A可明显抑制血管平滑肌增殖,使细胞阻滞在G0/G1期,其机制与抑制Mek-Erk1/2信号通路有关。Objective:To investigate the effect of Mfn21A on the proliferation of VSMC and its underlying mechanism. Method:The fragment sequence of Mfn21A contains the p21 ras signature motif and ATP/GTP binding site motif.VSMCs separated from spontaneously hypertensive rats were transfected with adenovirus mediated 1A(Adv-Mfn2 1A) or adenovirus mediated Mfn2(Adv-Mfn2).The proliferation of VSMC was detemined by cell counting and CCK-8.The cell cycle was analyzed by flow cytometry.The protein expression of Mek and Erk1/2 was determined by Western blot. Result:VSMCs tranfected with Adv-Mfn2 1A could express Mfn2 protein.Overexpression of Mfn21A inhibited the proliferation of VSMC more obviously than Mfn2 on day 3(P〈0.05).More cells were arrested at G0/G1 phases after Mfn2 1A and Mfn2 overexpression,and the percentage of cell that were arrested at G0/G1 phases was(77.74±3.67)% in Mfn21A transfection group.Overexpression of Mfn2 1A led to down regulation of P-Erk1/2,and this downregulation was more significant in Mfn21A transfection group than that of Mfn2 group(P〈0.05). Conclusion:Overexpression of Mfn2 1A inhibit the proliferation of on VSMC and induce cell cycle arrest at G0/G1 phases via inhibiting the Mek-Erk1/2 signaling pathway.
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