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化学伴侣拯救 Alport 综合征?

Chemical chaperones to the rescue of Alport syndrome?

机构信息

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Vanderbilt Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

出版信息

Kidney Int. 2024 Sep;106(3):359-361. doi: 10.1016/j.kint.2024.07.006.

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.

摘要

Alport 综合征是一种遗传性肾脏疾病,由胶原 IV 突变引起,这些突变干扰了α3α4α5 三聚体形成和沉积到肾小球基底膜中。在本期杂志中,于等人表明,化学伴侣熊去氧胆酸通过增加突变型α3α4α5 三聚体肾小球基底膜沉积和防止内质网应激诱导的足细胞凋亡,预防具有致病性错义突变的 Col4a3 突变小鼠的肾脏结构变化和功能下降。

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