miR-99a对高胰岛素诱导小鼠主动脉血管平滑肌细胞增殖的影响及机制研究

Effect of miR-99a on insulin-stimulated proliferation of vascular smooth muscle cells in mice and its mechanism

  • 摘要: 目的 观察miR-99a对高浓度胰岛素诱导小鼠主动脉血管平滑肌细胞(vascular smooth muscle cell,VSMC)增殖的影响及可能机制。 方法 原代培养小鼠主动脉血管平滑肌细胞,用超生理浓度剂量胰岛素(100 nmol/L)作用于血管平滑肌细胞,用荧光实时定量PCR (quantitative real-time PCR,qRT-PCR)检测miR-99a表达变化情况。Brdu法检测转染miR-99a对高胰岛素促细胞增殖的影响。qRT-PCR及Western blot检测转染miR-99a组及阴性对照组哺乳动物雷帕霉素靶蛋白(mammalian target of rapamycin,mTOR) mRNA及蛋白变化情况,并检测转染miR-99a对高胰岛素促进mTOR表达及对其下游通路激活的影响。Western blot检测转染miR-99a组及阴性对照组细胞周期素D1(CyclinD1)的变化。 结果 高浓度胰岛素显著降低miR-99a的表达。转染miR-99a mimic后可减少基础的及胰岛素促进的VSMC增殖作用。miR-99a负向调节mTOR mRNA及蛋白,转染miR-99a mimic可显著削弱高胰岛素促进的mTOR/P70S6K1通路激活作用,而转染miR-99a inhibitor可增加高胰岛素促进mTOR/p70s6k1通路激活作用。转染miR-99a mimic后可减少基础的及胰岛素促进的CyclinD1表达。 结论 miR-99a可通过负向调节mTOR抑制高胰岛素诱导的VSMC细胞增殖作用。

     

    Abstract: Objective To explore the effect of miR-99a on proliferation of insulin-stimulated vascular smooth muscle cell(VSMC) in mice and investigate its detailed mechanism. Methods The vascular smooth muscle cells derived from C57 mice were cultured by adherent method, and the cells were treated with 100 nmol/L of insulin for 48 h.Quantitative real-time PCR(qRT-PCR) was adopted to investigate the changes of miR-99a expression.Brdu assay was used to evaluate the effect of transfected miR-99a on insulininduced proliferation of VSMCs.qRT-PCR and western blot analysis were used to detect mRNA and protein expression changes of Mammalian target of rapamycin(mTOR) after miR-99a transfection in experimental group and negative control and explore the effect of miR-99a on insulin-enforced mTOR/P70S6K signaling pathway.And western blot analysis was used to detect the expression of CyclinD1 after miR-99a transfection in experimental group and negative control. Results High dose of insulin significantly decreased the expression of miR-99a.Transfection of miR-99a mimics remarkably attenuated basal and insulin-stimulated VSMCs proliferation, and downregulation insulin-activated mTOR/P70S6K signaling pathway and insulin-enforced expression of CyclinD1.In contrast, transfection of miR-99a inhibitors further enhanced insulin-activated mTOR/P70S6K signaling pathway. Conclusion MiR-99a can inhibit insulin-stimulated VSMC proliferation by downregulation of mTOR.

     

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