Article Text

Download PDFPDF
Extended report
Interleukin-6 and chondrocyte mineralisation act in tandem to promote experimental osteoarthritis
  1. Sonia Nasi1,
  2. Alexander So1,
  3. Christèle Combes2,
  4. Michel Daudon3,
  5. Nathalie Busso1
  1. 1Service of Rheumatology, Department of Musculoskeletal Medicine, CHUV and University of Lausanne, Lausanne, Switzerland
  2. 2CIRIMAT, UMR 5085 INPT-UPS-CNRS, Université de Toulouse, ENSIACET, Toulouse, France
  3. 3AP-HP, service d'Explorations Fonctionnelles, hôpital Tenon, Paris, France
  1. Correspondence to Dr Nathalie Busso, Laboratory of Rheumatology, Centre des Laboratoires d'Epalinges, CLE D04-404, Chemin des Boveresses 155, Epalinges 1066, Switzerland; Nathalie.Busso{at}


Objectives Basic calcium phosphate (BCP) crystal and interleukin 6 (IL-6) have been implicated in osteoarthritis (OA). We hypothesise that these two factors may be linked in a reciprocal amplification loop which leads to OA.

Methods Primary murine chondrocytes and human cartilage explants were incubated with hydroxyapatite (HA) crystals, a form of BCP, and the modulation of cytokines and matrix-degrading enzymes assayed. The ability of IL-6 to stimulate chondrocyte calcification was assessed in vitro. The mechanisms underlying the effects of HA on chondrocytes were investigated using chemical inhibitors, and the pathways mediating IL-6-induced calcification characterised by quantifying the expression of genes involved in chondrocyte mineralisation. The role of calcification in vivo was studied in the meniscectomy model of murine OA (MNX), and the link between IL-6 and cartilage degradation investigated by histology.

Results In chondrocytes, BCP crystals stimulated IL-6 secretion, further amplified in an autocrine loop, through signalling pathways involving Syk and PI3 kinases, Jak2 and Stat3 molecules. Exogenous IL-6 promoted calcium-containing crystal formation and upregulation of genes involved in calcification: the pyrophosphate channel Ank, the calcium channel Annexin5 and the sodium/phosphate cotransporter Pit-1. Treatment of chondrocytes with IL-6 inhibitors significantly inhibited IL-6-induced crystal formation. In meniscectomised mice, increasing deposits of BCP crystals were observed around the joint and correlated with cartilage degradation and IL-6 expression. Finally, BCP crystals induced proteoglycan loss and IL-6 expression in human cartilage explants, which were reduced by an IL-6 inhibitor.

Conclusions BCP crystals and IL-6 form a positive feedback loop leading to OA. Targeting calcium-containing crystal formation and/or IL-6 are promising therapeutic strategies in OA.

  • Osteoarthritis
  • Cytokines
  • Chondrocytes

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.