Selective induction of the secretion of cathepsins B and L by cytokines in synovial fibroblast-like cells

Br J Rheumatol. 1997 Jul;36(7):735-43. doi: 10.1093/rheumatology/36.7.735.

Abstract

We have investigated the potent influence of some cytokines, tumour necrosis factor-alpha (TNF-alpha), platelet-derived growth factor (PDGF), basic fibroblast growth factor (bFGF) and interferon-gamma (IFN-gamma), on the secretion of cysteine proteinases (cathepsins B and L) by cultured synovial fibroblast-like cells from patients with rheumatoid arthritis (RA). After treatment of synovial fibroblast-like cells with cytokines, culture media were evaluated for cathepsins B and L by enzyme immunoassays, and for cathepsin B and L activities using the enzymatic substrates. Z-Phe-Arg-AMC and Z-Arg-Arg-AMC, and specific inhibitors. Treatment of synovial fibroblast-like cells with TNF-alpha or PDGF resulted in a marked increase in cathepsin B secretion. Moreover, after prolonged PDGF treatment, the amount of secreted cathepsin B returned to the low control level. In contrast, bFGF led to increased cathepsin L secretion. IFN-gamma induced both cathepsin B and L secretion. Our results show that cytokines induce a selective secretion of cathepsins B and L by synovial fibroblast-like cells. This selective effect of cytokines on the secretion of cysteine proteinases suggests that synovial fibroblast-like cell-mediated articular degradation is a highly regulated process.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthritis, Rheumatoid / metabolism
  • Arthritis, Rheumatoid / pathology
  • Cathepsin B / analysis
  • Cathepsin B / genetics
  • Cathepsin B / metabolism*
  • Cathepsin L
  • Cathepsins / analysis
  • Cathepsins / genetics
  • Cathepsins / metabolism*
  • Cells, Cultured
  • Culture Media / chemistry
  • Cysteine Endopeptidases
  • Cytokines / pharmacology*
  • Dose-Response Relationship, Drug
  • Endopeptidases*
  • Enzyme-Linked Immunosorbent Assay
  • Fibroblast Growth Factor 2 / pharmacology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Gene Expression Regulation
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin-1 / pharmacology
  • Phenotype
  • Platelet-Derived Growth Factor / pharmacology
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Recombinant Proteins / pharmacology
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism*
  • Synovial Membrane / pathology
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Culture Media
  • Cytokines
  • Interleukin-1
  • Platelet-Derived Growth Factor
  • RNA, Messenger
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Fibroblast Growth Factor 2
  • Interferon-gamma
  • Cathepsins
  • Endopeptidases
  • Cysteine Endopeptidases
  • Cathepsin B
  • CTSL protein, human
  • Cathepsin L