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PMID: 17977705 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

The inflammasome: a danger sensing complex triggering innate immunity.

Current opinion in immunology ·Vol. 19 ·No. 6 ·2007-12-00 ·Pages 615-22

Pétrilli V, Dostert C, Muruve DA, Tschopp J

Abstract

The NOD-like receptors (NLR) are a family of intracellular sensors of microbial motifs and 'danger signals' that have emerged as being crucial components of the innate immune responses and inflammation. Several NLRs (NALPs and IPAF) form a caspase-1-activating multiprotein complex, termed inflammasome, that processes proinflammatory cytokines including IL-1beta. Amongst the various inflammasomes, the NALP3 inflammasome is particularly qualified to sense a plethora of diverse molecules, ranging from bacterial muramyldipeptide to monosodium urate crystals. The important role of the NALP3 inflammasome is emphasized by the identification of mutations in the NALP3 gene that are associated with a susceptibility to inflammatory disorders. These and other issues related to the inflammasome are discussed in this review.

MeSH Terms
Animals Antigens, Bacterial/immunology Carrier Proteins/immunology,metabolism Caspases/metabolism Cytokines/immunology,metabolism Humans Immunity, Innate Inflammation Mediators/immunology,metabolism NLR Family, Pyrin Domain-Containing 3 Protein Receptors, Pattern Recognition/immunology
Chemicals
Antigens, Bacterial Carrier Proteins Cytokines Inflammation Mediators NLR Family, Pyrin Domain-Containing 3 Protein NLRP3 protein, human Receptors, Pattern Recognition Caspases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Pétrilli Virginie
Department of Biochemistry, University of Lausanne, Ch des Boveresses 155, CH-1066, Epalinges, Switzerland.
Dostert Catherine
Muruve Daniel A
Tschopp Jürg
Article Info
Journal
Current opinion in immunology
Abbr.
Curr Opin Immunol
ISSN
0952-7915
Published
2007-12-00
Epub
2007-00-30
Pages
615-22
Language
English
Region
England
NLM ID
8900118
Subset
IM
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