Biphasic, Bidirectional Regulation of NF-κB by Endoplasmic Reticulum Stress

被引:0
作者
Kitamura, Masanori [1 ]
机构
[1] Univ Yamanashi, Dept Mol Signaling, Interdisciplinary Grad Sch Med & Engn, Chuo Ku, Yamanashi 4093898, Japan
基金
日本学术振兴会;
关键词
UNFOLDED-PROTEIN RESPONSE; NECROSIS-FACTOR-ALPHA; CARDIAC SARCOPLASMIC-RETICULUM; DEPENDENT GENE-EXPRESSION; OXIDE-INDUCED APOPTOSIS; PANCREATIC BETA-CELLS; ZINC-FINGER PROTEIN; NITRIC-OXIDE; ER STRESS; DNA-BINDING;
D O I
10.1089/ars.2008.2391
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
Endoplasmic reticulum (ER) stress induces an adaptive program called the unfolded protein response (UPR), which affects activity of an array of kinases and transcription factors. Previous reports provided evidence for activation of nuclear factor-kappa B (NF-kappa B), the major transcription factor regulating inflammatory processes, by ER stress. However, recent investigation also suggested that preceding ER stress suppresses activation of NF-kappa B by subsequent exposure to inflammatory stimuli. Although ER stress induces activation of NF-kappa Bin the early phase, consequent UPR may inhibit NF-kappa B-dependent cellular activation in the later phase. This article summarizes current knowledge on potential mechanisms underlying the biphasic, bidirectional regulation of NF-kappa B by ER stress. Antioxid. Redox Signal. 11, 2353-2364.
引用
收藏
页码:2353 / 2364
页数:12
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