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MicroRNA-146a negatively regulates PTGS2 expression induced by Helicobacter pylori in human gastric epithelial cells

机译:MicroRNA-146a 负调控人胃上皮细胞中幽门螺杆菌诱导的 PTGS2 表达

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Background: Helicobacter pylori is a major human pathogenic bacterium in the gastric mucosa, but to date the regulatory mechanism of the H. pylori-induced inflammatory response is not clear. MicroRNAs have recently emerged as key post-transcriptional regulators of gene expression. We have previously reported that miR-146a negatively regulates the H. pylori-induced inflammatory response, but its molecular mechanism is just beginning to be explored. Our aim was to further explore the key targets of miR-146a and its role of regulation in H. pylori infection. Methods: The potential targets of miR-146a were screened through bioinformatic approaches and identified by luciferase reporter assays and green fluorescent protein (GFP) repression experiments. Overexpression and inhibition of miR-146a were used to examine the impacts of miR-146a on its target gene, determined by quantitative real-time polymerase chain reaction (PCR) and western blotting. Results: Prostaglandin endoperoxide synthase 2 (PTGS2) is a target gene of miR-146a, and miR-146a decreased PTGS2 expression by degradation of its mRNA, suggesting that the miR-146a-mediated inhibition is a post-transcriptional event. Furthermore, miR-146a and PTGS2 were significantly increased in H. pylori -infected human gastric epithelial cells. Overexpression of miR-146a resulted in significantly reduced PTGS2 production induced by H. pylori infection. Conclusions: These results suggest that miR-146a may be involved in negatively regulating H. pylori-induced PTGS2 expression in human gastric epithelial cells. ? 2012 Springer.
机译:背景:幽门螺杆菌是胃黏膜中的主要人类致病菌,但迄今为止幽门螺杆菌诱导的炎症反应的调控机制尚不清楚。MicroRNA最近成为基因表达的关键转录后调节因子。我们之前已经报道过miR-146a负调控幽门螺杆菌诱导的炎症反应,但其分子机制才刚刚开始探索。我们的目的是进一步探讨miR-146a的关键靶点及其在幽门螺杆菌感染中的调控作用。方法:通过生物信息学方法筛选miR-146a的潜在靶点,并通过荧光素酶报告基因测定和绿色荧光蛋白(GFP)抑制实验进行鉴定。通过实时荧光定量聚合酶链反应(PCR)和蛋白质印迹法测定miR-146a的过表达和抑制miR-146a对其靶基因的影响。结果:前列腺素内过氧化物合酶2(PTGS2)是miR-146a的靶基因,miR-146a通过降解其mRNA降低PTGS2的表达,提示miR-146a介导的抑制是转录后事件。此外,miR-146a和PTGS2在幽门螺杆菌感染的人胃上皮细胞中显著增加。miR-146a 的过表达导致幽门螺杆菌感染诱导的 PTGS2 产生显着减少。结论:这些结果表明,miR-146a可能参与幽门螺杆菌诱导的人胃上皮细胞PTGS2表达的负调控。?2012 斯普林格。

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