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Publication Detail

Title: Differential ASC requirements reveal a key role for neutrophils and a noncanonical IL-1β response to Pseudomonas aeruginosa.

Authors: Patankar, Yash R; Mabaera, Rodwell; Berwin, Brent

Published In Am J Physiol Lung Cell Mol Physiol, (2015 Oct 15)

Abstract: The NLRC4 inflammasome is responsible for IL-1β processing by macrophages in response to Pseudomonas aeruginosa infection. We therefore hypothesized that mice that lack ASC, an NLRC4 inflammasome adaptor protein necessary for in vitro IL-1β production by macrophages, would be preferentially protected from a hyperinflammatory lethal challenge that is dependent on bacterial type three secretion system (T3SS) activity. We report herein that lack of ASC does not confer preferential protection in response to P. aeruginosa acute infection and that ASC(-/-) mice are capable of producing robust amounts of IL-1β comparable with C57BL/6 mice. We now identify that neutrophils represent the ASC-independent source of IL-1β production during the acute phases of infection both in models of acute pneumonia and peritonitis. Consequently, depletion of neutrophils in ASC(-/-) mice leads to a marked deficit in IL-1β production in vivo. The pulmonary neutrophil IL-1β response is predominantly dependent on caspase-1, which contrasts with data derived from ocular infection. These studies therefore identify a noncanonical mechanism of IL-1β production by neutrophils independent of ASC and demonstrate the first physiological contribution of neutrophils as an important source of IL-1β in response to acute P. aeruginosa infection during acute pneumonia and peritonitis.

PubMed ID: 26472815 Exiting the NIEHS site

MeSH Terms: Animals; Apoptosis Regulatory Proteins/deficiency; Apoptosis Regulatory Proteins/genetics; Apoptosis Regulatory Proteins/immunology*; CARD Signaling Adaptor Proteins; Calcium-Binding Proteins/deficiency; Calcium-Binding Proteins/genetics; Calcium-Binding Proteins/immunology; Disease Models, Animal; In Vitro Techniques; Inflammasomes/immunology; Interleukin-1beta/biosynthesis*; Mice; Mice, Inbred C57BL; Mice, Knockout; Neutrophils/immunology*; Neutrophils/microbiology*; Peritonitis/immunology; Pneumonia, Bacterial/immunology; Pseudomonas Infections/immunology; Pseudomonas aeruginosa/immunology*; Pseudomonas aeruginosa/pathogenicity*

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