Ligand-induced autoregulation of IFN-gamma receptor beta chain expression in T helper cell subsets

Science. 1995 Nov 17;270(5239):1215-8. doi: 10.1126/science.270.5239.1215.

Abstract

Interferon gamma (IFN-gamma) responsiveness in certain cells depends on the state of cellular differentiation or activation. Here an in vitro developmental system was used to show that IFN-gamma produced during generation of the CD4+ T helper cell type 1 (TH1) subset extinguishes expression of the IFN-gamma receptor beta subunit, resulting in TH1 cells that are unresponsive to IFN-gamma. This beta chain loss also occurred in IFN-gamma-treated TH2 cells and thus represents a specific response of CD4+ T cells to IFN-gamma rather than a TH1-specific differentiation event. These results define a mechanism of cellular desensitization where a cytokine down-regulates expression of a receptor subunit required primarily for signaling and not ligand binding.

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis*
  • Cell Differentiation
  • Cell Line
  • Cytokines / biosynthesis
  • Down-Regulation
  • Gene Expression
  • Genes, MHC Class I
  • Interferon gamma Receptor
  • Interferon-gamma / pharmacology*
  • Ligands
  • Mice
  • Mice, Transgenic
  • Receptors, Interferon / biosynthesis*
  • Th1 Cells / cytology
  • Th1 Cells / immunology
  • Th1 Cells / metabolism*
  • Th2 Cells / cytology
  • Th2 Cells / immunology
  • Th2 Cells / metabolism*

Substances

  • Antigens, CD
  • Cytokines
  • Ligands
  • Receptors, Interferon
  • Interferon-gamma