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Involvement of MicroRNAs in Hydrogen Peroxide-mediated Gene Regulation and Cellular Injury Response in Vascular Smooth Muscle Cells

机译:MicroRNA参与过氧化氢介导的基因调控。 和平滑肌细胞损伤反应 细胞

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摘要

MicroRNAs (miRNAs) comprise a novel class of endogenous, small, noncoding RNAs that negatively regulate ∼30% of genes in a cell via degradation or translational inhibition of their target mRNAs. However, the effects of reactive oxygen species (ROS) on miRNA expression and the roles of miRNAs in ROS-mediated gene regulation and biological functions of vascular cells are unclear. Using microarray analysis, we demonstrated that miRNAs are aberrantly expressed in vascular smooth muscle cells (VSMCs) after treatment with hydrogen peroxide (H2O2). H2O2-mediated up-regulation of microRNA-21 (miR-21) was further confirmed by quantitative real-time PCR. To determine the potential roles of miRNAs in H2O2-mediated gene regulation and cellular effects, miR-21 expression was down-regulated by miR-21 inhibitor and up-regulated by pre-miR-21. H2O2-induced VSMC apoptosis and death were increased by miR-21 inhibitor and decreased by pre-miR-21. Programmed cell death 4(PDCD4) was a direct target of miR-21 that was involved in miR-21-mediated effects on VSMCs. Pre-miR-21-mediated protective effect on VSMC apoptosis and death was blocked via adenovirus-mediated overexpression of PDCD4 without the miR-21 binding site. Moreover, activator protein 1 was a downstream signaling molecule of PDCD4 in miR-21-modulated VSMCs. The results suggest that miRNAs in VSMCs are sensitive to H2O2 stimulation. miRN-21 participates in H2O2-mediated gene regulation and cellular injury response through PDCD4 and the activator protein 1 pathway. miRNAs might play a role in vascular diseases related to ROS.
机译:MicroRNA(miRNA)包括一类新型的内源性,小的,非编码RNA,它们通过降解或翻译抑制其靶mRNA来负调控细胞中约30%的基因。但是,尚不清楚活性氧(ROS)对miRNA表达的影响以及miRNA在ROS介导的基因调控和血管细胞生物学功能中的作用。使用微阵列分析,我们证明了过氧化氢(H2O2)处理后,miRNA在血管平滑肌细胞(VSMC)中异常表达。 H2O2介导的microRNA-21(miR-21)的上调通过定量实时PCR进一步证实。为了确定miRNA在H2O2介导的基因调控和细胞效应中的潜在作用,miR-21的表达被miR-21抑制剂下调,而miR-21则被pre-miR-21上调。 H2O2诱导的VSMC凋亡和死亡被miR-21抑制剂增加,而被pre-miR-21减少。程序性细胞死亡4(PDCD4)是miR-21的直接靶标,它参与了miR-21介导的对VSMC的作用。 miR-21介导的对VSMC凋亡和死亡的保护作用通过腺病毒介导被阻断 没有miR-21结合位点的PDCD4的过表达。此外, 激活蛋白1是PDCD4的下游信号传导分子 miR-21调制的VSMC。结果表明VSMC中的miRNA是敏感的 对H2O2的刺激。 miRN-21参加 H2O2介导的基因调控和细胞损伤 通过PDCD4和激活蛋白1途径的应答。 miRNA可能发挥作用 在与ROS有关的血管疾病中起作用。

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