ER stress-induced cell death mechanisms

被引:1635
作者
Sano, Renata [1 ]
Reed, John C. [1 ]
机构
[1] Sanford Burnham Med Res Inst, La Jolla, CA 92037 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2013年 / 1833卷 / 12期
关键词
ER Stress; Cell death mechanisms; Diseases; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; THIOREDOXIN-INTERACTING PROTEIN; BAX INHIBITOR-1; AUTOPHAGOSOME FORMATION; INDUCED APOPTOSIS; MITOCHONDRIAL APOPTOSIS; ALZHEIMERS-DISEASE; GLUCOSE-METABOLISM; NLRP3; INFLAMMASOME;
D O I
10.1016/j.bbamcr.2013.06.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The endoplasmic-reticulum (ER) stress response constitutes a cellular process that is triggered by a variety of conditions that disturb folding of proteins in the ER. Eukaryotic cells have developed an evolutionarily conserved adaptive mechanism, the unfolded protein response (1)PR), which aims to clear unfolded proteins and restore ER homeostasis. In cases where ER stress cannot be reversed, cellular functions deteriorate, often leading to cell death. Accumulating evidence implicates ER stress-induced cellular dysfunction and cell death as major contributors to many diseases, making modulators of ER stress pathways potentially attractive targets for therapeutics discovery. Here, we summarize recent advances in understanding the diversity of molecular mechanisms that govern ER stress signaling in health and disease. This article is part of a Special Section entitled: Cell Death Pathways. Guest Editors: Frank Madeo and Slaven Stekovic. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:3460 / 3470
页数:11
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