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The effect of cyclic pressure on human monocyte-derived macrophages in vitro

G. M. Ferrier, FRCS, Clinical Lecturer in Orthopaedic Surgery; A. McEvoy, FRCS, Clinical Lecturer in Orthopaedic Surgery; C. E. Evans, PhD, Non-Clinical Lecturer in Orthopaedic Surgery; and J. G. Andrew, FRCS, Senior Lecturer in Orthopaedic Surgery

University of Manchester Musculoskeletal Research Group, Clinical Sciences Building, Hope Hospital, Stott Lane, Salford M6 8HD, UK.

Correspondence should be sent to Mr J. G. Andrew.

Aseptic loosening and osteolysis around prosthetic joints are the principal causes of failure and consequent revision. During this process activated macrophages produce cytokines which are thought to promote osteolysis by osteoclasts. Changes in pressure within the space around implants have been proposed as a cause of loosening and osteolysis. We therefore studied the effect of two different regimes of cyclic pressure on the production of interleukin-1ß (IL-1ß), IL-6 and tumour necrosis factor-{alpha} (TNF-{alpha}) by cultured human monocyte-derived (M-D) macrophages. There was a wide variation in the expression of cytokines in non-stimulated M-D macrophages from different donors and therefore cells from the same donor were compared under control and pressurised conditions.

Both regimes of cyclic pressure were found to increase expression of IL-6 and TNF-{alpha}. Expression of IL-1ß was increased by a higher-frequency regime only. Our findings suggest that M-D macrophages are activated by cyclic pressure. Further work will be required to understand the relative roles of frequency, amplitude and duration of applied pressure in the cellular effects of cyclic pressure in this system.




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Hip, Knee, Trauma, Upper limb, Foot & Ankle, Paediatrics, Oncology, Spine, Arthroplasty, General