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首页> 外文期刊>Renal failure. >Angiotensin II induces reorganization of the actin cytoskeleton and myosin light-chain phosphorylation in podocytes through rho/ROCK-signaling pathway
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Angiotensin II induces reorganization of the actin cytoskeleton and myosin light-chain phosphorylation in podocytes through rho/ROCK-signaling pathway

机译:血管紧张素II通过rho / ROCK信号通路诱导足细胞中肌动蛋白细胞骨架和肌球蛋白轻链磷酸化的重组

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摘要

Aims In the present study, we have evaluated the effect of angiotensin II (Ang II) on actin cytoskeleton reorganization and myosin light-chain (MLC) phosphorylation in podocytes to demonstrate whether the Rho/Rho-associated coiled kinase (ROCK) pathway is involved podocyte injury. Methods Eighteen male Sprague-Dawley rats were divided into three groups and treated with Ang II, saline or telmisartan. Morphological changes were studied at 28 days after treatment. Immunohistochemistry and Western blotting were used to determine the renal expression of p-MLC and ROCK2. Cultured podocytes were treated with Ang II (10(-7) M) with or without Rhokinase inhibitor (Y27632, 10(-6) M) for variable time periods. F-actin was visualized with fluorescein isothiocyanate (FITC)-conjugated phalloidin or tetraethyl rhodamine isothiocyanate (TRITC)-conjugated phalloidin. p-MLC expression was evaluated by immunofluorescence and Western blot. The activation of Rho/ROCK was evaluated by Western blot. Results The expression of p-MLC in glomeruli increased significantly in rats treated with Ang II when compared to the control rats as shown by Western blot (p<0.05). In cultured podocytes, Rho A and ROCK2 increased after incubation with Ang II. Ang II increased the expression of ROCK2, which was accompanied with altered morphology, redistribution of actin and increased phosphorylation of MLC. The distribution of actin changed to a large extent, although overall quantitative differences were not observed. Addition of Y-27632 to podocytes treated with Ang II could ameliorate F-actin cytoskeleton remodeling and the increment in p-MLC expression. Conclusion Ang II-induced podocyte cytoskeleton protein expression changing through the RhoA/ROCK2 p-MLC/F-actin pathway.
机译:目的在本研究中,我们评估了血管紧张素II(Ang II)对足细胞中肌动蛋白细胞骨架重组和肌球蛋白轻链(MLC)磷酸化的影响,以证明是否涉及Rho / Rho相关的卷曲激酶(ROCK)途径。足细胞损伤。方法将18只雄性Sprague-Dawley大鼠分为三组,分别用Ang II,盐水或替米沙坦治疗。在治疗后28天研究形态变化。免疫组织化学和蛋白质印迹法测定p-MLC和ROCK2的肾脏表达。将培养的足细胞用含或不含Rhokinase抑制剂(Y27632,10(-6)M)的Ang II(10(-7)M)进行可变时间段的处理。 F-肌动蛋白与异硫氰酸荧光素(FITC)结合的鬼笔环肽或异硫氰酸四乙基罗丹明异硫氰酸酯(TRITC)结合的鬼笔环肽可视化。通过免疫荧光和蛋白质印迹评估p-MLC表达。通过蛋白质印迹评估Rho / ROCK的活化。结果Western blot显示,与对照组相比,Ang II处理的大鼠肾小球中p-MLC的表达明显增加(p <0.05)。在培养的足细胞中,与Ang II孵育后,Rho A和ROCK2增加。 Ang II增加了ROCK2的表达,并伴随着形态的改变,肌动蛋白的重新分布和MLC磷酸化的增加。肌动蛋白的分布变化很大,尽管未观察到总体定量差异。在Ang II处理的足细胞中添加Y-27632可以改善F-肌动蛋白的细胞骨架重塑和p-MLC表达的增加。结论Ang II诱导的足细胞细胞骨架蛋白表达通过RhoA / ROCK2 p-MLC / F-肌动蛋白途径改变。

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