A role for IRF3-dependent RXRalpha repression in hepatotoxicity associated with viral infections

J Exp Med. 2006 Nov 27;203(12):2589-602. doi: 10.1084/jem.20060929. Epub 2006 Oct 30.

Abstract

Viral infections and antiviral responses have been linked to several metabolic diseases, including Reye's syndrome, which is aspirin-induced hepatotoxicity in the context of a viral infection. We identify an interferon regulatory factor 3 (IRF3)-dependent but type I interferon-independent pathway that strongly inhibits the expression of retinoid X receptor alpha (RXRalpha) and suppresses the induction of its downstream target genes, including those involved in hepatic detoxification. Activation of IRF3 by viral infection in vivo greatly enhances bile acid- and aspirin-induced hepatotoxicity. Our results provide a critical link between the innate immune response and host metabolism, identifying IRF3-mediated down-regulation of RXRalpha as a molecular mechanism for pathogen-associated metabolic diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Down-Regulation / genetics
  • Down-Regulation / immunology*
  • Gene Expression Regulation, Viral / immunology*
  • Hepatitis, Viral, Animal / genetics
  • Hepatitis, Viral, Animal / immunology
  • Hepatitis, Viral, Animal / metabolism*
  • Interferon Regulatory Factor-3 / physiology*
  • Mice
  • Mice, Knockout
  • Retinoid X Receptor alpha / antagonists & inhibitors*
  • Retinoid X Receptor alpha / biosynthesis
  • Retinoid X Receptor alpha / genetics
  • Reye Syndrome / genetics
  • Reye Syndrome / immunology
  • Reye Syndrome / virology
  • Rhabdoviridae Infections / genetics
  • Rhabdoviridae Infections / immunology
  • Rhabdoviridae Infections / metabolism
  • Vesicular stomatitis Indiana virus / immunology

Substances

  • Interferon Regulatory Factor-3
  • Irf3 protein, mouse
  • Retinoid X Receptor alpha