Role of intracellular calcium concentration and protein kinase C activation in IFN-gamma stimulation of U937 cells

J Immunol. 1990 Jun 1;144(11):4305-11.

Abstract

IFN-gamma enhances many monocyte functions, including oxidative metabolism and Ag presentation. IFN-gamma has been reported to increase the intracellular concentration of calcium ([Ca2+]i) and modulate protein kinase C activity in murine macrophages, but the signal transduction pathways induced by IFN-gamma in human cells and their functional significance are poorly understood. Our study examined the hypothesis that an increases in [Ca2+]i and protein kinase C activation are required for functional responses to IFN-gamma. The U937 cell line was used as a model of an IFN-gamma responsive cell. IFN-gamma caused a rapid and concentration-dependent increase in [Ca2+]i, which was partly inhibited by calcium-free medium, diltiazem, and TMB-8. IFN-gamma induced a fourfold increase in the concentration of inositol 1,4,5-trisphosphate. Induction of HLA-DR, Fc gamma R, CR3, and Mo3e Ag expression by IFN-gamma was blocked by concentrations of TMB-8 that inhibited an increase in [Ca2+]i, but not by protein kinase C inhibition by H-7 or inhibition of calmodulin with W-7. Ionomycin did not enhance Ag expression and PMA induced the expression of only the Mo3e Ag. We conclude that IFN-gamma induces antigenic expression on human U937 cells by a mechanism dependent on, but not limited to, an increase in intracellular calcium, which is likely due to inositol 1,4,5-trisphosphate generation.

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Antigens, Differentiation / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Antigens, Surface / metabolism*
  • Biological Transport
  • Calcium / physiology*
  • Cell Compartmentation
  • Cell Line
  • Enzyme Activation
  • Gallic Acid / analogs & derivatives
  • Gallic Acid / pharmacology
  • HLA-DR Antigens / metabolism
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Interferon-gamma / pharmacology*
  • Ionomycin / pharmacology
  • Isoquinolines / pharmacology
  • Macrophage-1 Antigen
  • Macrophages / physiology*
  • Piperazines / pharmacology
  • Protein Kinase C / physiology*
  • Receptors, Complement / metabolism
  • Receptors, Fc / metabolism
  • Receptors, IgG
  • Signal Transduction
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Antigens, Differentiation
  • Antigens, Differentiation, Myelomonocytic
  • Antigens, Surface
  • HLA-DR Antigens
  • Isoquinolines
  • Macrophage-1 Antigen
  • Piperazines
  • Receptors, Complement
  • Receptors, Fc
  • Receptors, IgG
  • Ionomycin
  • 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate
  • Gallic Acid
  • Interferon-gamma
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Inositol 1,4,5-Trisphosphate
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate
  • Calcium