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JLP/Foxk1/N-钙黏蛋白轴促进上皮管状细胞形成部分上皮-间质转化状态。

JLP/Foxk1/N-cadherin axis fosters a partial epithelial-mesenchymal transition state in epithelial tubular cells.

作者信息

Tian Maoqing, Zhang Lu, Zhang Meng, Qiao Liwen, Xu Bingqing, Li Chen, Liu Shan, Song Yuan, Wei Zhongping, Wang Yujuan, Wang Huiming

机构信息

Department of Nephrology, Renmin Hospital of Wuhan University, Wuhan, China.

Department of Nephrology, Minda Hospital, Affiliated with Hubei University for Nationalities, Enshi, China.

出版信息

iScience. 2023 Mar 14;26(4):106396. doi: 10.1016/j.isci.2023.106396. eCollection 2023 Apr 21.

Abstract

Renal tubular epithelial cells (TECs) undergoing partial epithelial-mesenchymal transition (pEMT) during renal fibrosis has been recognized as a featuring and detrimental event. However, the mechanism for redirecting the cell fate of pEMT remains unclear. Here we mapped the temporal expression trajectories of a series of EMT-related molecules in renal fibrosis. It revealed a unique expression profile of N-cadherin of initial rising and late dropdown, which is distinct from that of other mesenchymal markers. The transcription factor Foxk1, which serves as a negative regulator of the N-cadherin gene, was induced by TGF-β1 but was tightly regulated in the presence of JNK-associated leucine zipper protein (JLP). The loss of JLP resulted in Foxk1 induction, leading to N-cadherin downregulation and compromised cell viability. We propose a novel axis consisting of JLP/Foxk1/N-cadherin in shaping the EMT program and suggest JLP as the checkpoint of the EMT continuum during renal fibrosis progression.

摘要

肾纤维化过程中经历部分上皮-间质转化(pEMT)的肾小管上皮细胞(TECs)已被认为是一个典型且有害的事件。然而,重定向pEMT细胞命运的机制仍不清楚。在此,我们绘制了肾纤维化过程中一系列EMT相关分子的时间表达轨迹。它揭示了N-钙黏蛋白独特的表达谱,即先上升后下降,这与其他间充质标志物不同。转录因子Foxk1作为N-钙黏蛋白基因的负调节因子,由TGF-β1诱导,但在JNK相关亮氨酸拉链蛋白(JLP)存在的情况下受到严格调控。JLP的缺失导致Foxk1诱导,进而导致N-钙黏蛋白下调和细胞活力受损。我们提出了一个由JLP/Foxk1/N-钙黏蛋白组成的新轴,其在塑造EMT程序中发挥作用,并表明JLP是肾纤维化进展过程中EMT连续体的检查点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a2/10066564/76dfa5bf1353/fx1.jpg

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