Limiting inflammation-the negative regulation of NF-κB and the NLRP3 inflammasome

被引:826
作者
Afonina, Inna S. [1 ,2 ]
Zhong, Zhenyu [3 ,4 ]
Karin, Michael [3 ,4 ]
Beyaert, Rudi [1 ,2 ]
机构
[1] VIB, Unit Mol Signal Transduct Inflammat, Ctr Inflammat Res, Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, Ghent, Belgium
[3] Univ Calif San Diego, Lab Gene Regulat & Signal Transduct, Dept Pharmacol, Sch Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Pathol, Sch Med, La Jolla, CA 92093 USA
关键词
ONSET AUTOINFLAMMATORY DISEASE; INNATE IMMUNE-RESPONSES; SPATA2 LINKS CYLD; CELL-DEATH; IRAK-M; DEUBIQUITINATING ENZYME; SYSTEMIC INFLAMMATION; MESSENGER-RNAS; I INTERFERON; TNF-ALPHA;
D O I
10.1038/ni.3772
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
A properly mounted immune response is indispensable for recognizing and eliminating danger arising from foreign invaders and tissue trauma. However, the 'inflammatory fire' kindled by the host response must be tightly controlled to prevent it from spreading and causing irreparable damage. Accordingly, acute inflammation is self-limiting and is normally attenuated after elimination of noxious stimuli, restoration of homeostasis and initiation of tissue repair. However, unresolved inflammation may lead to the development of chronic autoimmune and degenerative diseases and cancer. Here, we discuss the key molecular mechanisms that contribute to the self-limiting nature of inflammatory signaling, with emphasis on the negative regulation of the NF-kappa B pathway and the NLRP3 inflammasome. Understanding these negative regulatory mechanisms should facilitate the development of much-needed therapeutic strategies for treatment of inflammatory and autoimmune pathologies.
引用
收藏
页码:861 / 869
页数:9
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