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Rapid induction of inflammatory lipid mediators by the inflammasome in vivo

VON MOLTKE, Jakob ; TRINIDAD, Norver J ; VANCE, Russell E ; MOAYERI, Mahtab ; KINTZER, Alexander F ; WANG, Samantha B ; ROOIJEN, Nico Van ; BROWN, Charles R ; KRANTZ, Bryan A ; LEPPLA, Stephen H ; GRONERT, Karsten

Nature (London), 2012-10, Vol.490 (7418), p.107-111 [Periódico revisado por pares]

London: Nature Publishing Group

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Título:
Rapid induction of inflammatory lipid mediators by the inflammasome in vivo
Autor: VON MOLTKE, Jakob ; TRINIDAD, Norver J ; VANCE, Russell E ; MOAYERI, Mahtab ; KINTZER, Alexander F ; WANG, Samantha B ; ROOIJEN, Nico Van ; BROWN, Charles R ; KRANTZ, Bryan A ; LEPPLA, Stephen H ; GRONERT, Karsten
Assuntos: Analytical, structural and metabolic biochemistry ; Animals ; Antigens, Bacterial - chemistry ; Antigens, Bacterial - genetics ; Antigens, Bacterial - metabolism ; Apoptosis Regulatory Proteins - deficiency ; Apoptosis Regulatory Proteins - metabolism ; Bacterial proteins ; Bacterial Toxins - chemistry ; Bacterial Toxins - genetics ; Bacterial Toxins - metabolism ; Biological and medical sciences ; Biosynthesis ; Body Fluids - metabolism ; Body Temperature ; Bone marrow ; Calcium Signaling ; Calcium-Binding Proteins - deficiency ; Calcium-Binding Proteins - metabolism ; Capillary Permeability ; Caspase 1 - deficiency ; Caspase 1 - metabolism ; Cellular signal transduction ; Cyclooxygenase 1 - deficiency ; Cytosol - metabolism ; Death ; Eicosanoids - biosynthesis ; Eicosanoids - metabolism ; Female ; Flagella (Microbiology) ; Flagellin - genetics ; Flagellin - immunology ; Flagellin - metabolism ; Fluid Shifts ; Fundamental and applied biological sciences. Psychology ; Hematocrit ; Immune system ; Immunity, Innate - immunology ; Infections ; Inflammasomes - metabolism ; Inflammation ; Inflammation - immunology ; Inflammation - metabolism ; Inflammation - pathology ; Interleukin-18 ; Interleukin-1beta ; Intestines - metabolism ; Legionella pneumophila ; Macrophages, Peritoneal - immunology ; Male ; Mice ; Mice, Inbred C57BL ; Molecular and cellular biology ; Neuronal Apoptosis-Inhibitory Protein - deficiency ; Neuronal Apoptosis-Inhibitory Protein - metabolism ; Pathology ; Peritoneal Cavity ; Peritoneal Lavage ; Properties ; Proteins ; Recombinant Fusion Proteins - genetics ; Recombinant Fusion Proteins - metabolism ; Rodents ; Salmonella Infections - immunology ; Salmonella typhimurium - immunology ; Time Factors
É parte de: Nature (London), 2012-10, Vol.490 (7418), p.107-111
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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Descrição: 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)-1β 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-1β 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.
Editor: London: Nature Publishing Group
Idioma: Inglês

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Rapid induction of inflammatory lipid mediators by the inflammasome in vivo

VON MOLTKE, Jakob ; TRINIDAD, Norver J ; VANCE, Russell E ; MOAYERI, Mahtab ; KINTZER, Alexander F ; WANG, Samantha B ; ROOIJEN, Nico Van ; BROWN, Charles R ; KRANTZ, Bryan A ; LEPPLA, Stephen H ; GRONERT, Karsten

London: Nature Publishing Group

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