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The kinase activity of PKR represses inflammasome activity.
Yim, Howard C H; Wang, Die; Yu, Liang; White, Christine L; Faber, Pieter W; Williams, Bryan R G; Sadler, Anthony J.
Afiliação
  • Yim HC; Centre for Cancer Research, Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria 3168, Australia.
  • Wang D; Department of Molecular and Translational Science, Monash University, Clayton, Victoria 3168, Australia.
  • Yu L; Centre for Cancer Research, Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria 3168, Australia.
  • White CL; Department of Molecular and Translational Science, Monash University, Clayton, Victoria 3168, Australia.
  • Faber PW; Centre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria 3168, Australia.
  • Williams BR; Department of Molecular and Translational Science, Monash University, Clayton, Victoria 3168, Australia.
  • Sadler AJ; Centre for Cancer Research, Hudson Institute of Medical Research, 27-31 Wright St, Clayton, Victoria 3168, Australia.
Cell Res ; 26(3): 367-79, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26794869
ABSTRACT
The protein kinase R (PKR) functions in the antiviral response by controlling protein translation and inflammatory cell signaling pathways. We generated a transgenic, knock-in mouse in which the endogenous PKR is expressed with a point mutation that ablates its kinase activity. This novel animal allows us to probe the kinase-dependent and -independent functions of PKR. We used this animal together with a previously generated transgenic mouse that is ablated for PKR expression to determine the role of PKR in regulating the activity of the cryopyrin inflammasome. Our data demonstrate that, in contradiction to earlier reports, PKR represses cryopyrin inflammasome activity. We demonstrate that this control is mediated through the established function of PKR to inhibit protein translation of constituents of the inflammasome to prevent initial priming during innate immune signaling. These findings identify an important role for PKR to dampen inflammation during the innate immune response and caution against the previously proposed therapeutic strategy to inhibit PKR to treat inflammation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: EIF-2 Quinase / Inflamassomos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: EIF-2 Quinase / Inflamassomos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article