4.6 Article

Cutting edge: Apoptosis-regulating signal kinase 1 is required for reactive oxygen species-mediated activation of IFN regulatory factor 3 by. lipopolysaccharide

Journal

JOURNAL OF IMMUNOLOGY
Volume 176, Issue 10, Pages 5720-5724

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.176.10.5720

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Funding

  1. NIAID NIH HHS [R56 AI047182, R01 AI047182, R01 AI047182-05, R01 AI047182-01, R01 AI047182-02, R01 AI047182-04, R01 AI 47182, R56 AI047182-06A1, R01 AI047182-03] Funding Source: Medline

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IFN regulatory factor (IRF) 3 participates in the transcriptional induction of IFN-alpha, IFN-beta, and a subset of IFN-stimulatedgenes (ISGs) as a result of viral infection. In addition, bacterial cell wall components such as LPS activate IRF3 in a p38-dependent manner. In this study we show that IRF3-mediated ISG induction by LPS requires the production of reactive oxygen species (ROS) by the NADPH-dependent oxidase NOX4. Furthermore, we present evidence that LPS-mediated ROS production leads to activation of apoptosis-regulating-signal kinase (ASK) 1, a MAPK kinase kinase family member capable of activating the MAP kinase 6/p38 axis. ASK1 kinase activity proved essential for IRF3-mediated/SG induction by LPS. Thus, our results presented here suggest a novel role for ROS and ASK1 in the innate immune response as signaling intermediates in the IRF3 activation pathway.

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