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Rheumatology Advance Access originally published online on July 6, 2004
Rheumatology 2004 43(10):1226-1231; doi:10.1093/rheumatology/keh296
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Rheumatology Vol. 43 No. 10 © British Society for Rheumatology 2004; all rights reserved

Paper

Effects of methotrexate on human bone cell responses to mechanical stimulation

K. J. Elliot, S. J. Millward-Sadler, M. O. Wright, J. E. Robb1, W. H. B. Wallace2 and D. M. Salter

Division of Pathology, University of Edinburgh Medical School, 1 Department of Orthopaedics and 2 Department of Oncology, Royal Hospital for Sick Children, Edinburgh, UK.

Correspondence to: D. M. Salter, Division of Pathology, Edinburgh University Medical School, Teviot Place, Edinburgh EH8 9AG, UK. E-mail: Donald.Salter{at}ed.ac.uk

Objectives. Methotrexate (MTX), which is prescribed in the treatment of malignancy and autoimmune disease, has detrimental effects on a number of organ systems, including bone. At present, the exact mechanism of action of MTX on bone at the cellular level is unclear. Mechanical stimuli imparted by stretch, pressure, fluid flow and shear stress result in a variety of biochemical responses that are important in bone metabolism. Cyclical mechanical stimulation at 0.33 Hz induces rapid cell membrane hyperpolarization of human bone cells (HBC) via an integrin-mediated pathway which includes an IL-1ß autocrine/paracrine loop. This study was undertaken to investigate the effect of MTX on responses of HBC to 0.33 Hz mechanical stimulation.

Methods. Electrophysiological responses of HBC were measured before and after mechanical stimulation at 0.33 Hz in the presence or absence of MTX. Semiquantitative RT–PCR was used to investigate effects of MTX on relative levels of type-1 collagen and bone morphogenetic protein-4 (BMP-4) following 0.33 Hz mechanical stimulation.

Results. MTX dose-dependently inhibited HBC hyperpolarization in response to 0.33 Hz mechanical stimulation. Production/release of IL-1ß was inhibited by MTX, whereas its effects on target cells were not. Mechanical stimulation of HBC at 0.33 Hz caused a significant decrease in relative levels of BMP-4 mRNA, whereas relative levels of type-1 collagen mRNA were consistently increased, although these increases did not reach statistical significance. These trends were unaffected by MTX.

Conclusions. These studies show that MTX affects HBC mechanotransduction by interfering with integrin-mediated signalling. The data also suggest that the mechanotransduction pathway responsible for the regulation of type-1 collagen and BMP-4 gene expression may be distinct from the IL-1ß-mediated signalling pathway.

KEY WORDS: Methotrexate, Integrin, Interleukin-1ß, Mechanical stimulation, Mechanotransduction, Gene expression


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