Inflammatory Caspases in Innate Immunity and Inflammation

被引:70
作者
Yazdi, Amir S. [1 ]
Guarda, Greta [1 ]
D'Ombrain, Marthe C. [1 ]
Drexler, Stefan K. [1 ]
机构
[1] Univ Lausanne, Dept Biochem, CH-1066 Epalinges, Switzerland
基金
英国医学研究理事会;
关键词
Apoptosis; Autoinflammatory diseases; Caspases; NLRs; Inflammation; Inflammasome; NF-KAPPA-B; INTERLEUKIN-1-BETA CONVERTING-ENZYME; PATTERN-RECOGNITION RECEPTORS; STRESS-INDUCED APOPTOSIS; PROTEINASE-INHIBITOR; 9; CELL-DEATH; NALP3; INFLAMMASOME; DOMAIN PROTEIN; NUCLEAR-FACTOR; LEGIONELLA-PNEUMOPHILA;
D O I
10.1159/000283688
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Caspases are best known for their role in apoptosis. More recently, they have gained prominence as critical mediators of innate immune responses. The so-called 'inflammatory caspases' include human caspase-1, -4, -5 and -12 and murine caspase-1, -11 and -12. Of these, caspase-1 is best characterized and serves as the prototype for our understanding of the processing, activation and function of inflammatory caspases. Like their apoptotic counterparts, inflammatory caspases are produced as inactive zynnogens and require activation to become proteolytically active. Caspase-1 is activated within the inflammasome, a large cytosolic protein complex that is induced by a growing number of endogenous, microbial, chemical or environmental stimuli. The importance of caspase-1 in initiating innate immune responses is demonstrated by its role in cleaving pro-IL-13 and pro-IL-18 to their biologically active forms. New functions have also been implicated, as these proteases and the mechanisms underlying their activation and regulation emerge as important mediators of human health and disease. Copyright (C) 2010 S Karger AG, Basel
引用
收藏
页码:228 / 237
页数:10
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