IFN-gamma production and cytotoxicity of IL-2-activated murine NK cells are differentially regulated by MHC class I molecules

J Immunol. 1999 Dec 15;163(12):6488-93.

Abstract

Activation of NK cells by target cells leads to cytotoxicity as well as production of various cytokines including IFN-gamma. MHC class I molecules on target cells regulate NK cytotoxicity. However, little is known about the regulation of IFN-gamma production by NK cells. We examined the production of IFN-gamma in individual murine NK cells stimulated with tumor cell lines by flow cytometric analysis of intracellular IFN-gamma. Among several tumor lines tested, the rat basophilic leukemia line RBL-1 induced particularly high level of IFN-gamma production in IL-2-activated NK cells, whereas other lines, including the prototypic NK target YAC-1, induced very low or no IFN-gamma production. Transfection of murine classical MHC class I molecules into RBL-1 cells substantially inhibited IFN-gamma production. This inhibition of IFN-gamma production by MHC class I was independent of Ly-49 or CD94/NKG2A expression on NK cells. These results indicate that some target cells directly stimulate IL-2-activated NK cells and induce IFN-gamma production, but the requirements for the induction of IFN-gamma production seem different from those for NK cytotoxicity. Furthermore, similar to NK cytotoxicity, induction of IFN-gamma production is inhibited by MHC class I on stimulating cells. However, the MHC class I-specific receptors inhibiting IFN-gamma production are different from those for NK cytotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Ly*
  • Binding Sites / immunology
  • Cytotoxicity, Immunologic*
  • Histocompatibility Antigens Class I / metabolism
  • Histocompatibility Antigens Class I / physiology*
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / biosynthesis*
  • Interleukin-2 / pharmacology*
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lectins, C-Type
  • Lymphocyte Activation*
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Rats
  • Receptors, Immunologic / biosynthesis
  • Receptors, Immunologic / metabolism
  • Receptors, KIR
  • Receptors, NK Cell Lectin-Like
  • Tumor Cells, Cultured

Substances

  • Antigens, Ly
  • Histocompatibility Antigens Class I
  • Interleukin-2
  • Lectins, C-Type
  • Membrane Glycoproteins
  • Receptors, Immunologic
  • Receptors, KIR
  • Receptors, NK Cell Lectin-Like
  • Interferon-gamma