Fas antigen expression on synovial cells was down-regulated by interleukin 1 beta

Biochem Biophys Res Commun. 1996 Jan 5;218(1):280-5. doi: 10.1006/bbrc.1996.0049.

Abstract

Recent reports revealed that Fas antigen is functionally expressed on human synovial cells and apoptosis can be induced in these cells by anti-Fas antibody. We examined the effect of interleukin 1 beta (IL-1 beta) on Fas antigen-mediated apoptosis on human synovial cells in vitro. Using flowcytometric analysis, IL-1 beta inhibited Fas antigen expression on synovial cells in a dose-dependent fashion. No significant difference of Fas antigen gene expression between IL-1 beta-treated and untreated synovial cells was observed by RT-PCR analysis, suggesting that the inhibitory effect of Fas antigen expression by IL-1 beta is at posttranscriptional level. Apoptosis of synovial cells was easily induced by treatment of these cells with anti-Fas antibody. In contrast, pretreatment of synovial cells with IL-1 beta protected these cells against Fas antigen-mediated apoptosis. The expression of bcl-2 on synovial cells, known to interfere with the apoptotic process mediated by the Fas antigen, was not influenced by IL-1 beta. Our results suggest that IL-1 beta inhibits Fas antigen-mediated apoptosis of synovial cells and may perpetuate the hyperplasia of the synovium in patients with rheumatoid arthritis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects
  • Arthritis, Rheumatoid / immunology*
  • Base Sequence
  • Cells, Cultured
  • DNA Primers
  • Flow Cytometry
  • Gene Expression Regulation* / drug effects
  • Humans
  • Interleukin-1 / pharmacology*
  • Kinetics
  • Lymphocytes / metabolism
  • Molecular Sequence Data
  • Osteoarthritis / immunology*
  • Polymerase Chain Reaction
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins c-bcl-2
  • Recombinant Proteins / pharmacology
  • Reference Values
  • Synovial Membrane / drug effects
  • Synovial Membrane / immunology*
  • Synovial Membrane / metabolism
  • fas Receptor / biosynthesis*

Substances

  • DNA Primers
  • Interleukin-1
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Recombinant Proteins
  • fas Receptor