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α-微管蛋白重新定位参与草酸钙诱导的肾上皮细胞紧密连接破坏。

Alpha-tubulin relocalization is involved in calcium oxalate-induced tight junction disruption in renal epithelial cells.

作者信息

Hadpech Sudarat, Peerapen Paleerath, Thongboonkerd Visith

机构信息

Medical Proteomics Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.

Medical Proteomics Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.

出版信息

Chem Biol Interact. 2022 Dec 1;368:110236. doi: 10.1016/j.cbi.2022.110236. Epub 2022 Oct 30.

Abstract

Microtubule (MT) is associated with tight junction (TJ) structure and function. While calcium oxalate monohydrate (COM) commonly causes TJ disruption, its effects on MT remain unknown. This study thus addressed the involvement of a major MT protein, α-tubulin, in COM-induced TJ disruption. Protein-protein interactions analysis demonstrated that α-tubulin directly interacted with a TJ protein, zonula occludens-1 (ZO-1). MDCK renal cells were polarized and incubated with COM crystals for 48 h. Western blotting showed that COM reduced ZO-1, but not α-tubulin, level. Immunofluorescence staining revealed COM-induced relocalization of α-tubulin from apical membranes to cytoplasm and ZO-1 disruption at cell borders. COM also mediated progressive fall of epithelial barrier function, represented by transepithelial resistance (TER), which reached the lowest at 12-h till the end of crystal exposure. Pretreatment of the cells with docetaxel, the MT/tubulin stabilizer, completely prevented such α-tubulin relocalization, ZO-1 disruption/down-regulation, and TER reduction. These data indicate that α-tubulin relocalization is involved in COM-induced TJ disruption in renal epithelial cells.

摘要

微管(MT)与紧密连接(TJ)的结构和功能相关。虽然一水合草酸钙(COM)通常会导致TJ破坏,但其对MT的影响尚不清楚。因此,本研究探讨了一种主要的MT蛋白α-微管蛋白在COM诱导的TJ破坏中的作用。蛋白质-蛋白质相互作用分析表明,α-微管蛋白直接与TJ蛋白紧密连接蛋白1(ZO-1)相互作用。将MDCK肾细胞极化并与COM晶体孵育48小时。蛋白质印迹显示COM降低了ZO-1水平,但未降低α-微管蛋白水平。免疫荧光染色显示COM诱导α-微管蛋白从顶端膜重新定位到细胞质,并导致细胞边界处的ZO-1破坏。COM还介导了上皮屏障功能的逐渐下降,以跨上皮电阻(TER)表示,在晶体暴露12小时直至结束时达到最低水平。用MT/微管蛋白稳定剂多西他赛预处理细胞,完全阻止了这种α-微管蛋白的重新定位、ZO-1破坏/下调以及TER降低。这些数据表明,α-微管蛋白的重新定位参与了COM诱导的肾上皮细胞TJ破坏。

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