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Published Online First: 2 September 2004. doi:10.1136/ard.2004.023135
Annals of the Rheumatic Diseases 2005;64:419-424
Copyright © 2005 BMJ Publishing Group Ltd & European League Against Rheumatism.
Annals of the Rheumatic Diseases 2005;64:419-424
© 2005 by BMJ Publishing Group Ltd & European League Against Rheumatism

EXTENDED REPORT

Galectin-3 is induced in rheumatoid arthritis synovial fibroblasts after adhesion to cartilage oligomeric matrix protein

M Neidhart1, F Zaucke2, R von Knoch1, A Jüngel1, B A Michel1, R E Gay1, S Gay1

1 Centre for Experimental Rheumatology, University Hospital, CH-8091 Zurich, Switzerland
2 Centre for Biochemistry, Medical Faculty, University of Cologne, D-50931 Cologne, Germany

Correspondence to:
Dr M Neidhart
Centre for Experimental Rheumatology, University Hospital, Gloriastrasse 25, CH-8091 Zurich, Switzerland; michel.neidhart{at}usz.ch

Background: Galectin-3 is expressed in the synovial tissue of patients with rheumatoid arthritis (RA), particularly at sites of joint destruction.

Objective: To explore the possibilities that galectin-3 is induced either by proinflammatory cytokines or by adhesion to cartilage components.

Methods: Cell culture plates were coated with fibronectin, collagens I–VI, or cartilage oligomeric matrix protein (COMP), and the suspended cells were then added. The medium was changed after 1 hour at 37°C. Adherent cells were further incubated for 18 hours in the presence or absence of tumour necrosis factor {alpha} (TNF{alpha}) or interleukin 1ß. Cells were pretreated with murine IgG1, anti-CD29, -CD51, -CD61 (integrins), or -CD3 monoclonal antibodies and transferred to culture plates coated with COMP. Adherent cells were counted by light microscopy. The expression of intracellular galectin-3, or cell surface CD29, CD51, and CD61 was determined by flow cytometry before and after adhesion.

Results: Four times more RA synovial fibroblasts (SF) than osteoarthritis SF adhered to COMP. RA SF presented more cell surface integrins, and monoclonal antibodies against CD51 inhibited the adhesion to COMP by 80%. TNF{alpha} reduced the expression of CD61 and the adhesion to COMP, but did not reverse the adhesion once it had taken place. The adhesion of RA SF to COMP was found to increase the intracellular level of galectin-3. In contrast, intracellular galectin-3 decreased after exposure to TNF{alpha}.

Conclusion: The increase of galectin-3 occurs after adhesion to COMP, and the {alpha}Vß3 receptor (CD51/CD61) has a pivotal role in this process.

Abbreviations: BSA, bovine serum albumin; CD29, integrin ß1; CD51, integrin {alpha}V; CD61, integrin ß3; COMP, cartilage oligomeric matrix protein; DMEM, Dulbecco’s modified Eagle’s medium; ECM, extracellular matrix; ELISA, enzyme linked immunosorbent assay; FACS, fluorescence activated cell sorting; FCS, fetal calf serum; FLI, fluorescence index; IL1ß, interleukin 1ß; OA, osteoarthritis; PBS, phosphate buffered saline; PE, phycoerythrin; RA, rheumatoid arthritis; SF, synovial fibroblasts; TNF{alpha}, tumour necrosis factor {alpha}; TSP-1, thrombospondin-1

Keywords: cartilage oligomeric matrix protein; galectin-3; integrins; rheumatoid arthritis


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