Up-modulation of interferon-gamma mediates the enhancement of spontanous cytotoxicity in prolactin-activated natural killer cells

Immunology. 1999 Nov;98(3):386-92. doi: 10.1046/j.1365-2567.1999.00893.x.

Abstract

Prolactin (PRL) has been shown to participate in lymphocyte activation. In particular, the constitutive natural killer (NK) and the lymphokine-activated killer (LAK) cytotoxicity of CD56+ CD16+ cells is increased by its physiological to supraphysiological concentrations. As PRL has been shown to up-regulate the production of interferon-gamma (IFN-gamma) by peripheral blood mononuclear cells, we studied its effect on IFN-gamma production by NK cells as a possible mechanism of autocrine activation of cytotoxicity. Released and intracellular IFN-gamma, as well as IFN-gamma mRNA expression, were increased by pituitary and recombinant human PRL, which stimulated optimal NK and LAK cytotoxicity. Treatment with blocking anti-IFN-gamma monoclonal antibody (mAb) selectively affected PRL-increased killing of K562 targets, demonstrating that PRL-mediated enhancement of spontaneous cytotoxicity depends, at least in part, on up-regulation of IFN-gamma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Autocrine Communication*
  • Cells, Cultured
  • Cytotoxicity, Immunologic*
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism*
  • Intracellular Fluid / metabolism
  • Killer Cells, Lymphokine-Activated / immunology
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology*
  • Prolactin / pharmacology*
  • RNA, Messenger / metabolism
  • Recombinant Proteins / pharmacology
  • Stimulation, Chemical

Substances

  • Antibodies, Monoclonal
  • RNA, Messenger
  • Recombinant Proteins
  • Interferon-gamma
  • Prolactin