Alternative and accessory pathways in the regulation of IFN-beta-mediated gene expression

J Interferon Cytokine Res. 2005 Dec;25(12):788-98. doi: 10.1089/jir.2005.25.788.

Abstract

Type I interferons (IFNs) induce the transcription of IFN-stimulated genes (ISGs) through activation of the Jak-Stat pathway. Although some determinants of specificity are dictated by the Jak-Stat components, recent observations indicate that the system incorporates other components for selectivity and flexibility, whose mechanisms remain to be defined. We identified a gene, beta-R1, which was induced relatively selectively by IFN-beta as compared with numerous IFN-alpha subtypes. Because all type I IFNs equally activate Jak-Stat signaling to IFN-stimulated gene factor 3 (ISGF3), this observation implied the existence of accessory signals for IFN-induced gene expression. We have used beta-R1 as a model system to examine this accessory signaling. In addition to Jak-Stat signaling for mediating IFN-induced cellular responses, p38 mitogen-activated protein kinase (p38 MAPK), phosphoinositol 3-kinase (PI3K), the IkappaB kinases (IKKs), and nuclear factor-kappaB (NF-kappaB) are some of the accessory components identified as required for the induction of certain IFN-beta-induced genes. This review focuses on the roles of accessory components in IFN-beta-mediated signaling, mechanisms of accessory signal generation, and how they modulate gene induction.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation*
  • Humans
  • Interferon-beta / metabolism*
  • MAP Kinase Signaling System
  • Models, Biological
  • NF-kappa B / metabolism
  • Phosphatidylinositol 3-Kinases / biosynthesis
  • Protein-Tyrosine Kinases / metabolism
  • Receptors, Interferon / metabolism
  • STAT Transcription Factors / metabolism
  • Signal Transduction
  • Transcriptional Activation
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • NF-kappa B
  • Receptors, Interferon
  • STAT Transcription Factors
  • Interferon-beta
  • Phosphatidylinositol 3-Kinases
  • Protein-Tyrosine Kinases
  • p38 Mitogen-Activated Protein Kinases