Constitutive IFN-alpha/beta signal for efficient IFN-alpha/beta gene induction by virus

Biochem Biophys Res Commun. 2001 Jul 13;285(2):518-25. doi: 10.1006/bbrc.2001.5159.

Abstract

Efficient IFN-alpha/beta gene induction in virus-infected cells is an event central to innate immunity, in which the transcription factor IRF-7 plays a critical role together with IRF-3. Unlike IRF-3, IRF-7 is short-lived and its gene expression is dependent on IFN-alpha/beta signalling; hence, the signal-dependent enhancement of IRF-7 gene induction during viral infection is essential for positive-feedback regulation of IFN-alpha/beta gene induction. Here, we provide evidence that constitutive, IRF-3/IRF-7-independent production of IFN-alpha/beta in uninfected cells is critical for setting the IRF-7 expression levels, determining whether or not the positive-feedback mechanism will operate effectively upon viral infection. In fact, spleen cells are more dependent than fibroblasts on this mechanism; the IFN-alpha/beta gene induction is impaired more severely by blocking the IRF-7 induction pathway than by introducing an IRF-3 null mutation. Thus, the constitutive IFN-alpha/beta signal provides a foundation for the IRF-7-mediated enhancement of its own production in response to virus infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Embryo, Mammalian
  • Fibroblasts / immunology
  • Fibroblasts / physiology
  • Fibroblasts / virology
  • Gene Expression Regulation / immunology*
  • Genetic Vectors
  • Interferon Regulatory Factor-3
  • Interferon Regulatory Factor-7
  • Interferon-alpha / genetics*
  • Interferon-beta / genetics*
  • Lymphocytes / immunology*
  • Mice
  • Mice, Knockout
  • Newcastle disease virus / immunology*
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spleen / immunology
  • Transcription Factors / deficiency
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic* / immunology
  • Transcriptional Activation
  • Transfection

Substances

  • DNA-Binding Proteins
  • Interferon Regulatory Factor-3
  • Interferon Regulatory Factor-7
  • Interferon-alpha
  • Irf3 protein, mouse
  • Irf7 protein, mouse
  • RNA, Messenger
  • Transcription Factors
  • Interferon-beta