Gliostatin/thymidine phosphorylase-regulated vascular endothelial growth-factor production in human fibroblast-like synoviocytes

Rheumatol Int. 2007 Apr;27(6):553-9. doi: 10.1007/s00296-006-0258-5. Epub 2006 Nov 14.

Abstract

Gliostatin/thymidine phosphorylase (GLS/TP) is known to have angiogenic and arthritogenic activities. The purpose of this study was to elucidate whether GLS/TP is involved in the regulation of the angiogenic cytokine vascular endothelial growth factor (VEGF) in rheumatoid arthritis (RA). Fibroblast-like synoviocytes (FLSs) from patients with RA were cultured and stimulated with recombinant human GLS (rHuGLS) and interleukin (IL)-1beta. Immunohistochemistry showed that GLS/TP and VEGF were detectable in the synovial lining cells. In cultured FLSs, both VEGF mRNA and protein levels were markedly increased by rHuIL-1beta treatment. rHuGLS increased VEGF mRNA expression in a dose-dependent manner. We detected high concentrations of VEGF165 protein in culture supernatants from FLSs treated with rHuGLS (300 ng/ml), which were comparable to GLS levels found in synovial fluid of RA patients. These findings indicate that GLS/TP and VEGF have synergistic effects on angiogenesis in rheumatoid synovitis, and that GLS/TP has a role in regulating VEGF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Arthritis, Rheumatoid / metabolism*
  • Arthritis, Rheumatoid / pathology*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Female
  • Fibroblasts / drug effects
  • Fibroblasts / enzymology
  • Fibroblasts / pathology*
  • Gene Expression / drug effects
  • Humans
  • Immunohistochemistry
  • In Vitro Techniques
  • Interleukin-1beta / pharmacology
  • Male
  • Middle Aged
  • RNA, Messenger / metabolism
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Synovial Membrane / enzymology
  • Synovial Membrane / pathology
  • Thymidine Phosphorylase / metabolism*
  • Thymidine Phosphorylase / pharmacology
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Interleukin-1beta
  • RNA, Messenger
  • Recombinant Proteins
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Thymidine Phosphorylase