疾病中的内质网应激。

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL MedComm Pub Date : 2024-08-26 DOI:10.1002/mco2.701
Yingying Liu, Chunling Xu, Renjun Gu, Ruiqin Han, Ziyu Li, Xianrong Xu
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引用次数: 0

摘要

内质网(ER)是真核细胞中的一个关键细胞器,负责多种重要功能,包括蛋白质的修饰、折叠和运输,以及脂质的生物合成和维持细胞内钙的平衡。各种因素都会破坏ER的功能,导致未折叠和折叠错误的蛋白质在ER内聚集,并诱发ER应激反应。为了减轻ER内的负担并恢复ER的平衡,一种称为未折叠蛋白反应(UPR)的保守信号事件级联逐渐发展起来。然而,当ER应激持续时间过长且水平升高时,这些过程可能最终导致细胞死亡。本综述总结了ER应激和UPR在各种疾病中决定细胞命运和功能的潜在作用,包括心血管疾病、神经退行性疾病、代谢性疾病、自身免疫性疾病、纤维化疾病、病毒感染和癌症。该研究还提出,操纵这一错综复杂的信号通路可能是药物发现和人类疾病创新治疗策略的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Endoplasmic reticulum stress in diseases

The endoplasmic reticulum (ER) is a key organelle in eukaryotic cells, responsible for a wide range of vital functions, including the modification, folding, and trafficking of proteins, as well as the biosynthesis of lipids and the maintenance of intracellular calcium homeostasis. A variety of factors can disrupt the function of the ER, leading to the aggregation of unfolded and misfolded proteins within its confines and the induction of ER stress. A conserved cascade of signaling events known as the unfolded protein response (UPR) has evolved to relieve the burden within the ER and restore ER homeostasis. However, these processes can culminate in cell death while ER stress is sustained over an extended period and at elevated levels. This review summarizes the potential role of ER stress and the UPR in determining cell fate and function in various diseases, including cardiovascular diseases, neurodegenerative diseases, metabolic diseases, autoimmune diseases, fibrotic diseases, viral infections, and cancer. It also puts forward that the manipulation of this intricate signaling pathway may represent a novel target for drug discovery and innovative therapeutic strategies in the context of human diseases.

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来源期刊
CiteScore
6.70
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审稿时长
10 weeks
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