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维甲酸受体α对缺氧诱导肾小管上皮细胞上皮间质转化及 TGF-β/MMP-9 通路的保护作用。

Protective effect of retinoic acid receptor α on hypoxia-induced epithelial to mesenchymal transition of renal tubular epithelial cells associated with TGF-β/MMP-9 pathway.

机构信息

Department of Pediatrics, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.

出版信息

Cell Biol Int. 2018 Aug;42(8):1050-1059. doi: 10.1002/cbin.10982. Epub 2018 May 29.

Abstract

Retinoic acid receptor α (RARα), a member of family of the nuclear retinoic acid receptors (RARs), plays an essential role in various chronic kidney diseases (CKD). Renal tubular epithelial to mesenchymal transition (EMT) is a common mechanism of progression of renal interstitial fibrosis (RIF). Hypoxia has been extensively considered as one of major inducers of renal tubular EMT. However, the effects of RARα on hypoxia-induced EMT have not yet been described so far. The aim of the present study was to explore the roles and potential mechanisms of RARα in hypoxia-induced EMT of renal tubular epithelial cells (RTECs). Our results showed that expression of RARα in RTECs subjected to hypoxia significantly was reduced, accompanied by decreased expression level of the epithelial marker E-cadherin, and increased expression levels of the mesenchymal markers α-smooth muscle actin (α-SMA) and vimentin, in accord with EMT. Meanwhile, hypoxia could cause RTECs to obviously express TGF-β and matrix metalloproteinase-9 (MMP-9). Furthermore, using lentivirus-based delivery vectors to overexpress RARα in RTECs, we demonstrated that RARα alleviated hypoxia-induced EMT of RTECs and downregulated the expression levels of TGF-β and MMP-9. In a word, RARα protects RTECs against EMT induced by hypoxia associated with TGF-β/MMP-9 pathway.

摘要

维甲酸受体α(RARα)是核维甲酸受体(RARs)家族的成员,在各种慢性肾脏病(CKD)中发挥着重要作用。肾小管上皮细胞向间充质转化(EMT)是肾间质纤维化(RIF)进展的常见机制。缺氧已被广泛认为是肾小管 EMT 的主要诱导因素之一。然而,到目前为止,RARα对缺氧诱导的 EMT 的影响尚未被描述。本研究旨在探讨 RARα在肾小管上皮细胞(RTECs)缺氧诱导的 EMT 中的作用及其潜在机制。我们的研究结果表明,缺氧处理的 RTECs 中 RARα的表达明显降低,伴随着上皮标志物 E-钙黏蛋白的表达水平降低,以及间充质标志物α-平滑肌肌动蛋白(α-SMA)和波形蛋白的表达水平升高,符合 EMT 特征。同时,缺氧可导致 RTECs 明显表达 TGF-β和基质金属蛋白酶-9(MMP-9)。此外,我们通过慢病毒载体过表达 RTECs 中的 RARα,证明 RARα减轻了 RTECs 缺氧诱导的 EMT,并下调了 TGF-β和 MMP-9的表达水平。总之,RARα通过 TGF-β/MMP-9 通路保护 RTECs 免受缺氧诱导的 EMT。

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