Production of interleukin-1 receptor antagonist, inflammatory chemotactic proteins, and prostaglandin E by rheumatoid and osteoarthritic synoviocytes--regulation by IFN-gamma and IL-4

J Immunol. 1994 Feb 15;152(4):2060-5.

Abstract

This study analyzes the effects of the T cell cytokines IL-4 and IFN-gamma on the spontaneous and stimulated production of IL-8, MCP-1, IL-1 receptor antagonist (IL-1ra), and PGE by synoviocytes from rheumatoid arthritis (RA) and osteoarthritis (OA) patients. Cells from both sources constitutively released IL-8 and MCP-1, but no IL-1ra or PGE. Stimulation with IL-1 beta or TNF-alpha massively increased chemokine production and induced the generation of PGE and low amounts of IL-1ra. The constitutive or cytokine-stimulated release of IL-8 was inhibited by IFN-gamma, but not by IL-4. The constitutive or IL-1 beta-stimulated release of MCP-1, by contrast, was markedly enhanced by IL-4 and IFN-gamma. Both cytokines, however, had only borderline effects on the release stimulated by TNF-alpha. The yield of IL-1ra was strongly enhanced by IFN-gamma in all cases, whereas the effect of IL-4 was pronounced only in IL-1 beta-stimulated OA synoviocytes. IL-4, on the other hand, markedly decreased the release of PGE, which was less susceptible to IFN-gamma. The observed effects on chemokines, IL-1ra expression, and PGE release by synoviocytes suggest that IFN-gamma and IL-4 are important regulatory elements in the inflamed synovium and may exert anti-inflammatory effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthritis, Rheumatoid / metabolism*
  • Cells, Cultured / drug effects
  • Chemokine CCL2
  • Chemotactic Factors / biosynthesis*
  • Cytokines / biosynthesis
  • Cytokines / pharmacology*
  • Female
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin 1 Receptor Antagonist Protein
  • Interleukin-4 / pharmacology
  • Male
  • Middle Aged
  • Osteoarthritis / metabolism*
  • Prostaglandins E / biosynthesis*
  • Sialoglycoproteins / biosynthesis*
  • Synovial Membrane / cytology
  • Synovial Membrane / metabolism

Substances

  • Chemokine CCL2
  • Chemotactic Factors
  • Cytokines
  • IL1RN protein, human
  • Interleukin 1 Receptor Antagonist Protein
  • Prostaglandins E
  • Sialoglycoproteins
  • Interleukin-4
  • Interferon-gamma