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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

机译:维甲酸受体α对缺氧诱导的肾小管上皮细胞间充质转换的保护作用,肾小管上皮细胞肾小管上皮细胞

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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.
机译:摘要视黄酸受体α(RARα),核视黄酸受体(RARS)的成员在各种慢性肾病(CKD)中起重要作用。间充质转换(EMT)肾小管上皮(EMT)是肾间质纤维化(RIF)进展的常见机制。缺氧被广泛被认为是肾小管EMT的主要诱导剂之一。然而,到目前为止尚未描述RARα对缺氧诱导的EMT的影响。本研究的目的是探讨RARα在缺氧诱导的肾小管上皮细胞(RECS)中的rARα的作用和潜在机制。我们的研究结果表明,在对缺氧进行的REC中的RARα表达显着降低,伴有上皮标记物E-Cadherin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Vimentin的表达水平增加。符合EMT。同时,缺氧可能导致RTEC明显表达TGF-β和基质金属蛋白酶-9(MMP-9)。此外,使用基于慢病毒的递送载体在RTEC中过表达RARα,我们证明RARα缓解缺氧诱导的rcES的EMT,并下调TGF-β和MMP-9的表达水平。总之,RARα保护rtecs针对与TGF-β/ MMP-9途径相关的缺氧诱导的EMT。

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