Publication Date:
2012-08-21
Description:
Detection of microbial products by host inflammasomes is an important mechanism of innate immune surveillance. Inflammasomes activate the caspase-1 (CASP1) protease, which processes the cytokines interleukin (IL)-1beta and IL-18, and initiates a lytic host cell death called pyroptosis. To identify novel CASP1 functions in vivo, we devised a strategy for cytosolic delivery of bacterial flagellin, a specific ligand for the NAIP5 (NLR family, apoptosis inhibitory protein 5)/NLRC4 (NLR family, CARD-domain-containing 4) inflammasome. Here we show that systemic inflammasome activation by flagellin leads to a loss of vascular fluid into the intestine and peritoneal cavity, resulting in rapid (less than 30 min) death in mice. This unexpected response depends on the inflammasome components NAIP5, NLRC4 and CASP1, but is independent of the production of IL-1beta or IL-18. Instead, inflammasome activation results, within minutes, in an 'eicosanoid storm'--a pathological release of signalling lipids, including prostaglandins and leukotrienes, that rapidly initiate inflammation and vascular fluid loss. Mice deficient in cyclooxygenase-1, a critical enzyme in prostaglandin biosynthesis, are resistant to these rapid pathological effects of systemic inflammasome activation by either flagellin or anthrax lethal toxin. Inflammasome-dependent biosynthesis of eicosanoids is mediated by the activation of cytosolic phospholipase A(2) in resident peritoneal macrophages, which are specifically primed for the production of eicosanoids by high expression of eicosanoid biosynthetic enzymes. Our results therefore identify eicosanoids as a previously unrecognized cell-type-specific signalling output of the inflammasome with marked physiological consequences in vivo.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3465483/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3465483/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉von Moltke, Jakob -- Trinidad, Norver J -- Moayeri, Mahtab -- Kintzer, Alexander F -- Wang, Samantha B -- van Rooijen, Nico -- Brown, Charles R -- Krantz, Bryan A -- Leppla, Stephen H -- Gronert, Karsten -- Vance, Russell E -- AI063302/AI/NIAID NIH HHS/ -- AI075039/AI/NIAID NIH HHS/ -- AI080749/AI/NIAID NIH HHS/ -- EY016136/EY/NEI NIH HHS/ -- EY022208/EY/NEI NIH HHS/ -- R01 EY016136/EY/NEI NIH HHS/ -- R01 EY022208/EY/NEI NIH HHS/ -- England -- Nature. 2012 Oct 4;490(7418):107-11. doi: 10.1038/nature11351. Epub 2012 Aug 19.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cell Biology, Division of Immunology and Pathogenesis, University of California at Berkeley, Berkeley, California 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22902502" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Antigens, Bacterial/chemistry/genetics/metabolism
;
Apoptosis Regulatory Proteins/deficiency/metabolism
;
Bacterial Toxins/chemistry/genetics/metabolism
;
Body Fluids/metabolism
;
Body Temperature
;
Calcium Signaling
;
Calcium-Binding Proteins/deficiency/metabolism
;
Capillary Permeability
;
Caspase 1/deficiency/metabolism
;
Cyclooxygenase 1/deficiency
;
Cytosol/metabolism
;
Death
;
Eicosanoids/*biosynthesis/metabolism
;
Female
;
Flagellin/genetics/immunology/metabolism
;
Fluid Shifts
;
Hematocrit
;
Immunity, Innate/immunology
;
Inflammasomes/*metabolism
;
Inflammation/immunology/metabolism/pathology
;
Interleukin-18
;
Interleukin-1beta
;
Intestines/metabolism
;
Legionella pneumophila
;
Macrophages, Peritoneal/immunology
;
Male
;
Mice
;
Mice, Inbred C57BL
;
Neuronal Apoptosis-Inhibitory Protein/deficiency/metabolism
;
Peritoneal Cavity
;
Peritoneal Lavage
;
Recombinant Fusion Proteins/genetics/metabolism
;
Salmonella Infections/immunology
;
Salmonella typhimurium/immunology
;
Time Factors
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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