ER chaperones in mammalian development and human diseases

被引:691
作者
Ni, Min [1 ]
Lee, Amy S. [1 ]
机构
[1] Univ So Calif, Dept Biochem & Mol Biol, USC Norris Comprehens Canc Ctr, Keck Sch Med, Los Angeles, CA 90089 USA
来源
FEBS LETTERS | 2007年 / 581卷 / 19期
关键词
endoplasmic reticulum; chaperones; mammalian; development; diseases;
D O I
10.1016/j.febslet.2007.04.045
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 field of endoplasmic reticulum (ER) stress in mammalian cells has expanded rapidly during the past decade, contributing to understanding of the molecular pathways that allow cells to adapt to perturbations in ER homeostasis. One major mechanism is mediated by molecular ER chaperones which are critical not only for quality control of proteins processed in the ER, but also for regulation of ER signaling in response to FIR stress. Here, we summarized the properties and functions of GRP78/BiP, GRP94/gp96, GRP170/ORP150, GRP58/ERp57, PDI, ERp72, calnexin, calreticulin, EDEM, Herp and co-chaperones SILI and P58(IPK) and their role in development and diseases. Many of the new insights are derived from recently constructed mouse models where the genes encoding the chaperones are genetically altered, providing invaluable tools for examining the physiological involvement of the ER chaperones in vivo. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3641 / 3651
页数:11
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