Chemical chaperones to the rescue of Alport syndrome?

IF 14.8 1区 医学 Q1 UROLOGY & NEPHROLOGY Kidney international Pub Date : 2024-08-20 DOI:10.1016/j.kint.2024.07.006
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Abstract

Alport syndrome is a hereditary kidney disease caused by collagen IV mutations that interfere with the formation and deposition of the α3α4α5 protomer into the glomerular basement membrane. In this issue, Yu et al. show that the chemical chaperone tauroursodeoxycholic acid prevented kidney structural changes and function decline in mice with a pathogenic missense Col4a3 mutation by increasing mutant α3α4α5 protomer glomerular basement membrane deposition and preventing podocyte apoptosis induced by endoplasmic reticulum stress.

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化学伴侣拯救阿尔波特综合征?
阿尔波特综合征是一种遗传性肾病,由胶原蛋白Ⅳ突变引起,这种突变干扰了α3α4α5原体在肾小球基底膜上的形成和沉积。在本期杂志中,Yu 等人的研究表明,化学伴侣牛磺脱氧胆酸通过增加突变α3α4α5 原球体肾小球基底膜沉积和防止内质网应激诱导的荚膜细胞凋亡,防止了致病性错义 Col4a3 突变小鼠肾脏结构的改变和功能的下降。
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来源期刊
Kidney international
Kidney international 医学-泌尿学与肾脏学
CiteScore
23.30
自引率
3.10%
发文量
490
审稿时长
3-6 weeks
期刊介绍: Kidney International (KI), the official journal of the International Society of Nephrology, is led by Dr. Pierre Ronco (Paris, France) and stands as one of nephrology's most cited and esteemed publications worldwide. KI provides exceptional benefits for both readers and authors, featuring highly cited original articles, focused reviews, cutting-edge imaging techniques, and lively discussions on controversial topics. The journal is dedicated to kidney research, serving researchers, clinical investigators, and practicing nephrologists.
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