首页> 美国卫生研究院文献>The Journal of Biological Chemistry >TGF-β-induced MiR-491-5p Expression Promotes Par-3 Degradation in Rat Proximal Tubular Epithelial Cells
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TGF-β-induced MiR-491-5p Expression Promotes Par-3 Degradation in Rat Proximal Tubular Epithelial Cells

机译:TGF-β诱导的MiR-491-5p表达促进大鼠近端肾小管上皮细胞中的Par-3降解

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摘要

Par-3 is a component of Par complex, which is critical for the integrity of tight junction. We previously reported that TGF-β down-regulated Par-3 expression in rat proximal tubular epithelial cells, but the underlying mechanism remains unknown. In the present study, we demonstrated by a luciferase reporter assay that miR-491-5p down-regulated the luciferase activity through a binding site in the 3′ UTR of Par-3. Overexpression of miR-491-5p dramatically decreased the expression of endogenous Par-3, disrupted tight junction, and resulted in decreased transepithelial resistance. Moreover, miR-491-5p expression was induced by TGF-β1 through the MEK/p38 MAPK pathway. Importantly, miR-491-5p levels were increased significantly in a rat model of obstructive nephropathy, in parallel with decreased Par-3 levels. Taken together, we conclude that up-regulation of miR-491-5p contributes to TGF-β-regulated Par-3 expression. Our study uncovered a novel mechanism by which TGF-β disrupts cell junction.
机译:Par-3是Par配合物的组成部分,这对于紧密连接的完整性至关重要。我们以前曾报道过TGF-β下调了大鼠近端肾小管上皮细胞中Par-3的表达,但其潜在机制尚不清楚。在本研究中,我们通过萤光素酶报告基因检测证明,miR-491-5p通过Par-3的3'UTR中的结合位点下调了萤光素酶活性。 miR-491-5p的过表达显着降低了内源性Par-3的表达,破坏了紧密连接,并导致跨上皮抵抗力降低。此外,TGF-β1通过MEK / p38 MAPK途径诱导miR-491-5p表达。重要的是,在阻塞性肾病大鼠模型中,miR-491-5p水平显着增加,而Par-3水平降低。两者合计,我们得出结论,miR-491-5p的上调有助于TGF-β调节的Par-3表达。我们的研究发现了TGF-β破坏细胞连接的新机制。

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