Cytokines regulate fibroblast-like synovial cell differentiation to adipocyte-like cells

Rheumatology (Oxford). 2004 Apr;43(4):448-52. doi: 10.1093/rheumatology/keh092. Epub 2004 Jan 20.

Abstract

Objectives: Our recent work showed that fibroblast-like synovial cells (FLS) could differentiate into adipocyte-like cells in vitro in response to stimulation with peroxisome proliferator-activated receptor gamma (PPAR gamma) ligand. The aim of the present study was to determine the role of cytokines in the regulation of FLS differentiation to adipocyte-like cells.

Methods: FLS isolated from patients with rheumatoid arthritis (RA) and osteoarthritis (OA) and from normal synovial tissues were incubated with the synthetic PPAR gamma ligand troglitazone to induce adipocyte-like differentiation of the cells.

Results: Production of interleukin (IL)-6, IL-8 and matrix metalloproteinase-3 was reduced in adipocyte-like cells compared with FLS. DNA binding activity of nuclear factor kappa B (NF-kappa B) was clearly inhibited in adipocyte-like cells. Cultivation of FLS with interferon gamma (IFN-gamma), tumour necrosis factor-alpha (TNF-alpha) or IL-1 beta inhibited the expression of PPAR gamma as well as CCAAT/enhancer binding protein (C/EBP) nuclear activity, and thus suppressed adipocyte-like cell differentiation in vitro.

Conclusion: Our results indicate the importance of PPAR gamma and C/EBP in adipocyte-like cell differentiation of FLS and that the process is influenced by inflammatory cytokines, and suggest that the proinflammatory character of FLS in patients with RA is diminished during adipocyte-like cell differentiation.

MeSH terms

  • Adipocytes / metabolism
  • Adipocytes / pathology
  • Arthritis, Rheumatoid / pathology*
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Chromans / pharmacology
  • Cytokines / physiology*
  • Fibroblasts / pathology*
  • Humans
  • Interleukin-6 / biosynthesis
  • Interleukin-8 / biosynthesis
  • Matrix Metalloproteinase 3 / biosynthesis
  • Osteoarthritis / pathology*
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Synovial Membrane / pathology*
  • Thiazolidinediones / pharmacology
  • Transcription Factors / metabolism
  • Troglitazone

Substances

  • Chromans
  • Cytokines
  • Interleukin-6
  • Interleukin-8
  • Receptors, Cytoplasmic and Nuclear
  • Thiazolidinediones
  • Transcription Factors
  • Matrix Metalloproteinase 3
  • Troglitazone