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IRE1α Signaling Pathways Involved in Mammalian Cell Fate Determination.

Authors :
Jie Wu
Guang-Ting He
Wei-Jin Zhang
Jing Xu
Qiao-Bing Huang
Source :
Cellular Physiology & Biochemistry (Karger AG). May2016, Vol. 38 Issue 5, p847-858. 12p.
Publication Year :
2016

Abstract

A diverse array of cellular stresses can lead to accumulation of misfolded or unfolded proteins in endoplasmic reticulum (ER), which subsequently elicits ER stress. Inositol-requiring enzyme 1a (IRE1α) is the most sensitive of the three unfolded protein response (UPR) branches which are triggered to cope with ER stress in mammalian cells. IRE1α signaling is quite contextspecific on account of many adaptor and modulator proteins that directly interact with it, including heat shock proteins (HSPs), RING finger protein 13 (RNF13), poly (ADP-ribose) polymerase 16 (PARP16), Bax/Bak, and Bax inhibitor-1 (BI-1). The activated IRE1α triggers different downstream pathways depending on the UPRosome formed by distinct modulator proteins. At the initial phase of ER stress, IRE1α-XBP1 axis functions as an adaptive response. While ER stress sustains or intensifies, signals shift to apoptotic responses. Furthermore, IRE1α signaling can be exploited to the development of a wide range of prevalent human diseases, with cancer the most characterized. Here we provide an overview of recent insights into the complex IRE1α signaling network which makes IRE1α an intriguing cell fate switch. Besides, the functional relevance is presented since IRE1α activation also participates in some other physiological processes beyond protein-folding status. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10158987
Volume :
38
Issue :
5
Database :
Academic Search Index
Journal :
Cellular Physiology & Biochemistry (Karger AG)
Publication Type :
Academic Journal
Accession number :
114165537
Full Text :
https://doi.org/10.1159/000443039