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The transcription factor IRF1 and guanylate-binding proteins target activation of the AIM2 inflammasome by Francisella infection.
Man, Si Ming; Karki, Rajendra; Malireddi, R K Subbarao; Neale, Geoffrey; Vogel, Peter; Yamamoto, Masahiro; Lamkanfi, Mohamed; Kanneganti, Thirumala-Devi.
Afiliação
  • Man SM; 1] Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA. [2] School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, Australia.
  • Karki R; Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Malireddi RK; Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Neale G; Hartwell Center for Bioinformatics &Biotechnology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Vogel P; Animal Resources Center and the Veterinary Pathology Core, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
  • Yamamoto M; Department of Microbiology and Immunology, Osaka University, Osaka, Japan.
  • Lamkanfi M; 1] Department of Medical Protein Research, Vlaams Instituut voor Biotechnologie, Ghent, Belgium. [2] Department of Biochemistry, Ghent University, Ghent, Belgium.
  • Kanneganti TD; Department of Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Nat Immunol ; 16(5): 467-75, 2015 May.
Article em En | MEDLINE | ID: mdl-25774715
ABSTRACT
Inflammasomes are critical for mounting host defense against pathogens. The molecular mechanisms that control activation of the AIM2 inflammasome in response to different cytosolic pathogens remain unclear. Here we found that the transcription factor IRF1 was required for activation of the AIM2 inflammasome during infection with the Francisella tularensis subspecies novicida (F. novicida), whereas engagement of the AIM2 inflammasome by mouse cytomegalovirus (MCMV) or transfected double-stranded DNA did not require IRF1. Infection of F. novicida detected by the DNA sensor cGAS and its adaptor STING induced type I interferon-dependent expression of IRF1, which drove the expression of guanylate-binding proteins (GBPs); this led to intracellular killing of bacteria and DNA release. Our results reveal a specific requirement for IRF1 and GBPs in the liberation of DNA for sensing by AIM2 depending on the pathogen encountered by the cell.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tularemia / Proteínas de Ligação ao GTP / Proteínas de Ligação a DNA / Fator Regulador 1 de Interferon / Inflamassomos / Francisella tularensis Limite: Animals Idioma: En Revista: Nat Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tularemia / Proteínas de Ligação ao GTP / Proteínas de Ligação a DNA / Fator Regulador 1 de Interferon / Inflamassomos / Francisella tularensis Limite: Animals Idioma: En Revista: Nat Immunol Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Austrália