Volume 54, Issue 7 pp. 2084-2095
Research Article

Regulation of pre–B cell colony-enhancing factor by STAT-3–dependent interleukin-6 trans-signaling: Implications in the pathogenesis of rheumatoid arthritis

Mari A. Nowell

Corresponding Author

Mari A. Nowell

Cardiff University School of Medicine, Cardiff, UK

Medical Biochemistry and Immunology, Tenovus Building, School of Medicine, Heath Park Campus, Cardiff University, Cardiff CF14 4XN, UKSearch for more papers by this author
Peter J. Richards

Peter J. Richards

Cardiff University School of Medicine, Cardiff, UK

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Ceri A. Fielding

Ceri A. Fielding

Cardiff University School of Medicine, Cardiff, UK

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Simona Ognjanovic

Simona Ognjanovic

Tissue Genesis, Honolulu, Hawaii

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Nick Topley

Nick Topley

Cardiff University School of Medicine, Cardiff, UK

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Anwen S. Williams

Anwen S. Williams

Cardiff University School of Medicine, Cardiff, UK

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Gillian Bryant-Greenwood

Gillian Bryant-Greenwood

John A. Burns School of Medicine, University of Hawaii, Honolulu

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Simon A. Jones

Simon A. Jones

Cardiff University School of Medicine, Cardiff, UK

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First published: 27 June 2006
Citations: 140

Abstract

Objective

To determine whether interleukin-6 (IL-6) trans-signaling directs the expression of pre–B cell colony-enhancing factor (PBEF) in vitro and in vivo.

Methods

Complementary DNA from rheumatoid arthritis (RA) synovial fibroblasts treated with IL-6 and soluble IL-6 receptor (sIL-6R) was used to probe a cytokine microarray. PBEF regulation by the IL-6–related cytokines, IL-6, sIL-6R, oncostatin M (OSM), IL-11, and leukemia inhibitory factor (LIF) was determined by reverse transcription–polymerase chain reaction analysis. IL-6–mediated STAT-3 regulation of PBEF was determined using a cell-permeable STAT-3 inhibitor peptide. Antigen-induced arthritis (AIA) was induced in wild-type (IL-6+/+) and IL-6–deficient (IL-6−/−) mice. PBEF and STAT were detected by immunohistochemistry, immunoblotting, and electrophoretic mobility shift assay. Synovial levels of PBEF were quantified by enzyme immunoassay.

Results

IL-6 trans-signaling regulated PBEF in a STAT-3–dependent manner. In addition, PBEF was regulated by the IL-6–related cytokine OSM, but not IL-11 or LIF. Flow cytometric analysis of the IL-6–related cognate receptors suggested that OSM regulates PBEF via its OSM receptor β and not its LIF receptor. The involvement of PBEF in arthritis progression was confirmed in vivo, where induction of AIA resulted in a 4-fold increase in the synovial expression of PBEF. In contrast, little or no change was observed in IL-6−/− mice, in which the inflammatory infiltrate was markedly reduced and synovial STAT-1/3 activity was also impaired. Analysis of human RA synovial tissue confirmed that PBEF immunolocalized in apical synovial membrane cells, endothelial cells, adipocytes, and lymphoid aggregates. Synovial fluid levels of PBEF were significantly higher in RA patients than in osteoarthritis patients.

Conclusion

Experiments presented herein demonstrate that PBEF is regulated via IL-6 trans-signaling and the IL-6–related cytokine OSM. PBEF is also actively expressed during arthritis. Although these data confirm an involvement of PBEF in disease progression, the consequence of its action remains to be determined.

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