Inflammatory caspases and inflammasomes: master switches of inflammation.

Details

Serval ID
serval:BIB_4BAF54017B93
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Inflammatory caspases and inflammasomes: master switches of inflammation.
Journal
Cell Death and Differentiation
Author(s)
Martinon F., Tschopp J.
ISSN
1350-9047 (Print)
ISSN-L
1350-9047
Publication state
Published
Issued date
2007
Volume
14
Number
1
Pages
10-22
Language
english
Abstract
Fifteen years have passed since the cloning and characterization of the interleukin-1beta-converting enzyme (ICE/caspase-1), the first identified member of a family of proteases currently known as caspases. Caspase-1 is the prototypical member of a subclass of caspases involved in cytokine maturation termed inflammatory caspases that also include caspase-4 caspase -5, caspase -11 and caspase -12. Efforts to elucidate the molecular mechanisms involved in the activation of these proteases have uncovered an important role for the NLR family members, NALPs, NAIP and IPAF. These proteins promote the assembly of multiprotein complexes termed inflammasomes, which are required for activation of inflammatory caspases. This article will review some evolutionary aspects, biochemical evidences and genetic studies, underlining the role of inflammasomes and inflammatory caspases in innate immunity against pathogens, autoinflammatory syndromes and in the biology of reproduction.
Keywords
Adaptor Proteins, Signal Transducing/metabolism, Amino Acid Sequence, Animals, Apoptosis Regulatory Proteins/metabolism, Caspases/genetics, Caspases/metabolism, Endoplasmic Reticulum/metabolism, Enzyme Activation, Humans, Immunity, Innate, Inflammation/metabolism, Interleukin-1beta/metabolism, Molecular Sequence Data, Multiprotein Complexes/metabolism, Reproduction, Sepsis/immunology
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 15:18
Last modification date
20/08/2019 13:59
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