Caspase-I: The inflammasome and beyond

被引:196
作者
Sollberger, Gabriel [1 ]
Strittmatter, Gerhard E. [1 ]
Garstkiewicz, Martha [1 ]
Sand, Jennifer [1 ]
Beer, Hans-Dietmar [1 ]
机构
[1] Univ Zurich Hosp, Dept Dermatol, CH-8006 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
GAMMA-INDUCING FACTOR; KAPPA-B ACTIVATION; HOST-CELL DEATH; IL-1-BETA-CONVERTING ENZYME; NLRP3; INFLAMMASOME; DIFFERENTIAL REQUIREMENT; AUTOINFLAMMATORY DISEASE; SIGNAL-TRANSDUCTION; IL-18; SECRETION; INNATE IMMUNITY;
D O I
10.1177/1753425913484374
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
Caspase-1 plays a fundamental role in innate immunity and in several important inflammatory diseases as the protease activates the pro-inflammatory cytokines proIL-1β and proIL-18. Caspase-1 itself is activated in different inflammasome complexes, which assemble in response to a variety of exogenous and endogenous stressors. More recently, pyroptosis, a caspase-1-dependent type of programmed cell death, has been identified that is able to support secreted IL-1 and IL-18 in triggering an inflammatory response. Whereas these 'canonical' activities are well appreciated, this review also highlights less-known pathways and molecules activated by caspase-1. There is evidence that caspase-1 supports cell survival by activation of NF-κB, induction of membrane repair and regulation of unconventional secretion of certain proteins. The physiologic effects of processing of other downstream targets, such as proteins involved in glycolysis or activation of caspase-7, are less well understood. However, there is increasing evidence that caspase-1 contributes to innate and adaptive immunologic defense mechanisms, repair and pathologic conditions by the regulation of several different and partially opposing pathways. © The Author(s) 2013 Reprints and permissions: sagepub.co.uk/journalsPermissions.nav.
引用
收藏
页码:115 / 125
页数:11
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