Deregulated inflammasome signaling in disease

被引:125
作者
Lamkanfi, Mohamed [2 ,3 ]
Vande Walle, Lieselotte [2 ,3 ]
Kanneganti, Thirumala-Devi [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38104 USA
[2] Univ Ghent, Dept Biochem, B-9000 Ghent, Belgium
[3] VIB, Dept Med Prot Res, Ghent, Belgium
关键词
NLR; inflammasome; NLRP3; ASC; caspase-1; autoimmunity; INTERLEUKIN-1-BETA CONVERTING-ENZYME; COLD AUTOINFLAMMATORY SYNDROME; DEXTRAN SULFATE SODIUM; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; ALPHA-DEFENSIN EXPRESSION; GENOME-WIDE ASSOCIATION; MUCKLE-WELLS-SYNDROME; GAMMA-INDUCING FACTOR; NF-KAPPA-B; CROHNS-DISEASE;
D O I
10.1111/j.1600-065X.2011.01042.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammasomes are multi-protein complexes that sense microbial molecules and endogenous danger signals in intracellular compartments. Inflammasome assembly results in caspase-1 activation, which in turn drives maturation and secretion of the pro-inflammatory cytokines interleukin 1 beta (IL-1 beta) and IL-18, and induces pyroptosis to eliminate the infectious agent. The importance of inflammasomes in regulating immune responses was recognized with the discovery of polymorphisms in genes encoding inflammasome components and their linkage to aberrant production of IL-1 beta and IL-18 in autoimmune and hereditary periodic fevers syndromes. We review the current knowledge on the role of inflammasomes in regulating innate and adaptive immune responses with an emphasis on the role of these immune complexes in autoinflammatory disorders and autoimmune diseases such as colitis, type I diabetes, multiple sclerosis and vitiligo.
引用
收藏
页码:163 / 173
页数:11
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