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蛋白尿性肾脏疾病:足细胞裂孔隔膜与细胞骨架研究方法

Proteinuric Kidney Diseases: A Podocyte's Slit Diaphragm and Cytoskeleton Approach.

作者信息

Yu Samuel Mon-Wei, Nissaisorakarn Pitchaphon, Husain Irma, Jim Belinda

机构信息

Department of Medicine, Jacobi Medical Center, Bronx, NY, United States.

Department of Medicine, James J. Peters VA Medical Center, Bronx, NY, United States.

出版信息

Front Med (Lausanne). 2018 Sep 11;5:221. doi: 10.3389/fmed.2018.00221. eCollection 2018.

Abstract

Proteinuric kidney diseases are a group of disorders with diverse pathological mechanisms associated with significant losses of protein in the urine. The glomerular filtration barrier (GFB), comprised of the three important layers, the fenestrated glomerular endothelium, the glomerular basement membrane (GBM), and the podocyte, dictates that disruption of any one of these structures should lead to proteinuric disease. Podocytes, in particular, have long been considered as the final gatekeeper of the GFB. This specialized visceral epithelial cell contains a complex framework of cytoskeletons forming foot processes and mediate important cell signaling to maintain podocyte health. In this review, we will focus on slit diaphragm proteins such as nephrin, podocin, TRPC6/5, as well as cytoskeletal proteins Rho/small GTPases and synaptopodin and their respective roles in participating in the pathogenesis of proteinuric kidney diseases. Furthermore, we will summarize the potential therapeutic options targeting the podocyte to treat this group of kidney diseases.

摘要

蛋白尿性肾脏疾病是一组病理机制多样的疾病,与尿液中蛋白质的大量丢失有关。肾小球滤过屏障(GFB)由三个重要层组成,即有窗孔的肾小球内皮、肾小球基底膜(GBM)和足细胞,这表明这些结构中任何一个的破坏都应导致蛋白尿性疾病。特别是足细胞,长期以来一直被认为是肾小球滤过屏障的最后一道防线。这种特殊的脏层上皮细胞含有形成足突的复杂细胞骨架框架,并介导重要的细胞信号传导以维持足细胞的健康。在本综述中,我们将重点关注缝隙隔膜蛋白,如nephrin、podocin、TRPC6/5,以及细胞骨架蛋白Rho/小GTP酶和突触足蛋白,以及它们在参与蛋白尿性肾脏疾病发病机制中的各自作用。此外,我们将总结针对足细胞治疗这组肾脏疾病的潜在治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0ff/6141722/7611a7f31e92/fmed-05-00221-g0001.jpg

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