Interleukin 2 down-modulates the macrophage colony-stimulating factor receptor in murine macrophages

Cytokine. 1996 Jun;8(6):488-94. doi: 10.1006/cyto.1996.0066.

Abstract

Macrophage colony-stimulating factor (M-CSF) is the main growth factor for mononuclear phagocytes. Responsiveness to growth factors is reduced in the course of functional activation of macrophages. We studied the interference of the macrophage activator interleukin 2 (IL-2) with the response to M-CSF, in macrophages of the M-CSF-dependent murine line BAC-1.2F5. Long-term effects of IL-2 on cell growth were determined, showing that IL-2 reduces the M-CSF-dependent proliferation of macrophages. Short-term effects of IL-2 on the expression of the receptor for M-CSF (M-CSF.R) were characterized in more detail. IL-2 rapidly down-modulated M-CSF.R in a dose-dependent fashion, and interferon-gamma and lipopolysaccharides synergized with IL-2 in this modulation. The IL-2-induced down-modulation of M-CSF.R was shown to require the activity of protein-kinase-C and phospholipase-C. The data are consistent with the hypothesis that the down-modulation of M-CSF.R is a general property of macrophage activators.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Down-Regulation / drug effects*
  • Drug Synergism
  • Interferon-gamma / pharmacology
  • Interleukin-2 / pharmacology*
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Mice
  • Protein Kinase C / metabolism
  • Receptor, Macrophage Colony-Stimulating Factor / metabolism*
  • Type C Phospholipases / metabolism

Substances

  • Interleukin-2
  • Lipopolysaccharides
  • Interferon-gamma
  • Receptor, Macrophage Colony-Stimulating Factor
  • Protein Kinase C
  • Type C Phospholipases