IRE1: ER stress sensor and cell fate executor

被引:416
|
作者
Chen, Yani
Brandizzi, Federica [1 ]
机构
[1] Michigan State Univ, MSU DOE Plant Res Lab, E Lansing, MI 48824 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
unfolded protein response; ER stress; IRE1; cell fate; protein quality control; membrane trafficking system; UNFOLDED PROTEIN RESPONSE; ENDOPLASMIC-RETICULUM STRESS; MESSENGER-RNA; LIPID-METABOLISM; ARABIDOPSIS-THALIANA; TRANSCRIPTION FACTOR; NLRP3; INFLAMMASOME; BAX INHIBITOR-1; MAMMALIAN-CELLS; IRE1-ALPHA;
D O I
10.1016/j.tcb.2013.06.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells operate a signaling network termed the unfolded protein response (UPR) to monitor protein-folding capacity in the endoplasmic reticulum (ER). Inositol-requiring enzyme 1 (IRE1) is an ER transmembrane sensor that activates the UPR to maintain the ER and cellular function. Although mammalian IRE1 promotes cell survival, it can initiate apoptosis via decay of antiapoptotic miRNAs. Convergent and divergent IRE1 characteristics between plants and animals underscore its significance in cellular homeostasis. This review provides an updated scenario of the IRE1 signaling model, discusses emerging IRE1 sensing mechanisms, compares IRE1 features among species, and outlines exciting future directions in UPR research.
引用
收藏
页码:547 / 555
页数:9
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