IL-27 synthesis induced by TLR ligation critically depends on IFN regulatory factor 3

J Immunol. 2007 Jun 15;178(12):7607-15. doi: 10.4049/jimmunol.178.12.7607.

Abstract

IL-27 is a heterodimeric cytokine composed of EBV-induced gene 3 and p28. Produced by dendritic cells (DCs) in response to TLR ligands, IL-27 recently emerged as a key regulator of inflammatory responses. In this study, we first demonstrate that Toll/IL-1R-containing adaptor inducing IFN-beta and its associated IFN regulatory factor (IRF) 3 transcription factor are critically involved in IL-27p28 expression in mouse DCs stimulated by TLR ligands. We then show that IL-27 serum levels are dramatically reduced in IRF3(-/-) upon LPS injection, indicating a critical role for IRF3 in TLR4-mediated IL-27 production in vivo. We identified an IRF3-binding site within the IL-27p28 promoter region which is required for IL-27p28 gene activation in reporter gene assays. In human DCs, IL-27p28 mRNA was preferentially induced by Toll/IL-1R-containing adaptor inducing IFN-beta-coupled TLR ligands and following CMV infection. Furthermore, chromatin immunoprecipitation studies demonstrate that IRF3 is recruited to the endogenous p28 promoter in TLR4-stimulated human DCs. We conclude that IRF3 activation is a master switch for IL-27 synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism*
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Chromatin Immunoprecipitation
  • Dendritic Cells / immunology
  • Gene Expression Regulation*
  • Humans
  • Interferon Regulatory Factor-3 / genetics
  • Interferon Regulatory Factor-3 / metabolism*
  • Interferon-beta / metabolism
  • Interleukins / biosynthesis
  • Interleukins / blood
  • Interleukins / genetics*
  • Lipopolysaccharides / immunology
  • Mice
  • Minor Histocompatibility Antigens
  • Molecular Sequence Data
  • Myeloid Differentiation Factor 88 / metabolism
  • Promoter Regions, Genetic
  • Receptors, Cytokine / genetics
  • Receptors, Interleukin-1 / metabolism
  • Toll-Like Receptor 4 / agonists
  • Toll-Like Receptors / metabolism
  • Transcriptional Activation

Substances

  • Adaptor Proteins, Vesicular Transport
  • Ebi3 protein, mouse
  • Il27 protein, mouse
  • Interferon Regulatory Factor-3
  • Interleukins
  • Lipopolysaccharides
  • Minor Histocompatibility Antigens
  • Myeloid Differentiation Factor 88
  • Receptors, Cytokine
  • Receptors, Interleukin-1
  • TICAM-1 protein, mouse
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Interferon-beta