Objective: While ultra-high molecular weight polyethylene (UHMWPE) wear particles are known to cause periprosthetic osteolysis, its interaction with other intra-articular tissues in the case of partial joint arthroplasties is not well understood. We hypothesized that UHMWPE particles per se would interact with intra-articular tissue, which by acting as inflammatory reservoirs, would subsequently induce osteoarthritic (OA) changes. Our goal was to assess the inflammatory response, phagocytic activity, as well as apoptosis of intra-articular cells in the presence of UHMWPE particles in vitro, and the in vivo response of those tissues after intra-articular injection of particles in a murine model. Design: Three cell types were used for the in vitro study; chondrocytes, meniscal fibrochondrocytes, and synoviocytes. Each cell type was cultured with two different concentrations of UHMWPE particles. Proinflammatory cytokine production, phagocytosis, and apoptosis were analyzed. In vivo experiments were done by injecting two concentrations of UHMWPE particles into normal and murine OA model knee joints. Results: In vitro experiments showed that UHMWPE particles increase pro-inflammatory cytokine and mediator (IL-1 beta, IL-6, TNF-alpha, Nitric Oxide, and Prostaglandin E2) production, phagocytosis of particles, and apoptosis in all cell types. In vivo experiment showed degeneration of cartilage and meniscus, as well as synovitis after particle injection. Conclusions: UHMWPE wear particles per se exert detrimental effects in cartilage, synovium, and meniscus of the knee joint resulting in pro-inflammatory cytokine release, phagocytosis of particles and apoptosis. Particles induced and exacerbated OA changes in a murine model. (C) 2013 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
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Orthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
El Bagdadi, K.
Muschter, D.
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Univ Regensburg, Dept Orthopaed Surg, Expt Orthopaed, Ctr Med Biotechnol, Regensburg, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Muschter, D.
Taheri, S.
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Univ Med Gottingen, Clin Trauma Surg Orthopaed Surg & Plast Surg, Gottingen, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Taheri, S.
Dorn, C.
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Univ Regensburg, Inst Pharm, Regensburg, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Dorn, C.
Schilling, A. F.
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Univ Med Gottingen, Clin Trauma Surg Orthopaed Surg & Plast Surg, Gottingen, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Schilling, A. F.
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Graessel, S.
Meurer, A.
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Orthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Meurer, A.
Zaucke, F.
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Orthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Zaucke, F.
Straub, R. H.
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Univ Hosp Regensburg, Dept Internal Med 1, Lab Expt Rheumatol & Neuroendocrine Immunol, Regensburg, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany
Straub, R. H.
Jenei-Lanzl, Z.
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Orthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, GermanyOrthoped Univ Hosp Friedrichsheim gGmbH, Dr Rolf M Schwiete Res Unit Osteoarthritis, Frankfurt, Germany