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MiR-155 contributes to intestinal barrier dysfunction in DSS-induced mice colitis via targeting HIF-1α/TFF-3 axis

机译:MIR-155通过靶向HIF-1α/ TFF-3轴有助于DSS诱导的小鼠结肠炎的肠道阻隔功能障碍

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摘要

Intestinal barrier dysfunction is a hallmark of inflammatory bowel disease (IBD). MiR-155 is increased in colitis and downregulates expression of hypoxia-inducible factor 1α (HIF-1α). Here, we investigated the effects of miR-155 on intestinal barrier dysfunction in dextran sulfate sodium (DSS)-induced colitis. We found that miR-155 antagomir treatment relieved weight loss and intestinal damage in IBD mouse models (P < 0.05). Furthermore, electron microscopy and immunofluorescence imaging showed that miR-155 increased intestinal barrier dysfunction and downregulated the expression of tight junction proteins in DSS-induced colitis. FG-4497, which upregulates HIF-1α expression, elicited protective effects on the intestinal barrier in DSS-induced colitis. Dual luciferase reporter assays also confirmed that miR-155 downregulated expression of HIF-1α. Finally, we discovered that HIF-1α levels were elevated by miR-155 antagomir treatment (P < 0.05) and that TFF-3 expression correlated positively with HIF-1α expression. These results suggest that miR-155 contributes to DSS-induced colitis by promoting intestinal barrier dysfunction and inhibiting the HIF-1α/TFF-3 axis.
机译:肠道屏障功能障碍是炎症性肠病(IBD)的标志。 miR-155在结肠炎中增加,并且下调缺氧诱导因子1α(HIF-1α)的表达。在这里,我们研究了miR-155对硫酸葡聚糖钠(DSS)诱导的结肠炎肠道屏障功能障碍的影响。我们发现MiR-155抗蛋白治疗在IBD小鼠模型中减轻了减肥和肠道损伤(P <0.05)。此外,电子显微镜和免疫荧光成像表明,MIR-155增加了肠道屏障功能障碍,并下调了DSS诱导的结肠炎中紧密结蛋白的表达。 FG-4497,其上调HIF-1α表达,引发了对DSS诱导的结肠炎肠道屏障的保护作用。双荧光素酶报告结果还证实MIR-155下调了HIF-1α的表达。最后,我们发现HIF-1α水平通过miR-155抗肿瘤治疗(P <0.05)升高,并且TFF-3表达与HIF-1α表达正相关。这些结果表明miR-155通过促进肠道屏障功能障碍和抑制HIF-1α/ TFF-3轴来促进DSS诱导的结肠炎。

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