IL-6 trans-signalling directly induces RANKL on fibroblast-like synovial cells and is involved in RANKL induction by TNF-alpha and IL-17

Rheumatology (Oxford). 2008 Nov;47(11):1635-40. doi: 10.1093/rheumatology/ken363. Epub 2008 Sep 11.

Abstract

Objectives: We investigated the influence of cytokines on the expression of RANK ligand (RANKL) in fibroblast-like synoviocytes from RA patients (RA-FLS).

Methods: RA-FLS were stimulated by IL-6, TNF-alpha, IL-17 and IL-1beta with or without soluble IL-6 receptor (sIL-6R) for 24 h. The expression of RANKL was measured by real-time PCR, western blotting and immunostaining. In proliferation assay, RA-FLS were cultured with cytokines for 3 days. RA-FLS were co-cultured with RAW cell in the presence of IL-6/sIL-6R for 3 days and then NFATc1 mRNA expression in RAW cells was examined. RA-FLS was cultured with parthenolide [PAR, signal transducer and activator of transcription (STAT) inhibitor] or PD98059 (PD, mitogen-activated protein kinase inhibitor) in the presence of IL-6/sIL-6R and then the influence of these drugs on phosphorylation of STAT3 and ERK1/2, and RANKL expression was examined.

Results: RANKL expression was induced by IL-6/sIL-6R (but not IL-6 alone) and by IL-1beta. On the other hand, TNF-alpha and IL-17 did not induce RANKL expression, although TNF-alpha, IL-17 or IL-1beta stimulated cell growth and IL-6 production. However, in the presence of sIL-6R, TNF-alpha or IL-17 induced RANKL expression. By the co-culture of RA-FLS, NFATc1 mRNA expression was induced in RAW cells. Finally, IL-6/sIL-6R induced phosphorylation of STAT3 and ERK1/2 in RA-FLS, and was completely inhibited by PAR and PD, respectively. PAR completely inhibited IL-6/sIL-6R-induced RANKL expression, but PD did not.

Conclusions: IL-6/sIL-6R directly induced RANKL expression in RA-FLS and it is essential for RANKL induction by TNF-alpha and IL-17. Moreover, RANKL induction by IL-6/sIL-6R is mediated by the janus kinase/STAT signalling pathway.

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal, Humanized
  • Arthritis, Rheumatoid / metabolism*
  • Blotting, Western / methods
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Fibroblasts
  • Flavonoids / pharmacology
  • Humans
  • Immunohistochemistry
  • Interleukin-17 / pharmacology*
  • Interleukin-1beta / pharmacology
  • Interleukin-6 / metabolism*
  • Interleukin-6 / pharmacology
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Phosphorylation / drug effects
  • RANK Ligand / analysis
  • RANK Ligand / genetics
  • RANK Ligand / metabolism*
  • RNA, Messenger / analysis
  • Receptor Activator of Nuclear Factor-kappa B / metabolism
  • Receptors, Interleukin-6 / antagonists & inhibitors
  • Receptors, Interleukin-6 / metabolism
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • STAT3 Transcription Factor / metabolism
  • Sesquiterpenes / pharmacology
  • Signal Transduction / physiology
  • Stimulation, Chemical
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Flavonoids
  • Interleukin-17
  • Interleukin-1beta
  • Interleukin-6
  • RANK Ligand
  • RNA, Messenger
  • Receptor Activator of Nuclear Factor-kappa B
  • Receptors, Interleukin-6
  • Recombinant Proteins
  • STAT3 Transcription Factor
  • Sesquiterpenes
  • Tumor Necrosis Factor-alpha
  • parthenolide
  • Mitogen-Activated Protein Kinase Kinases
  • tocilizumab
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one