Objective During osteoarthritis progression, cartilage degrades in a manner that influences its biomechanical and biotribological properties, while chondrocytes reduce the synthesis of extracellular matrix components and become apoptotic. This study investigates the effects of inflammation on cartilage under biomechanical stress using biotribological tests. Methods Bovine osteochondral grafts from five animals were punched out from the medial condyle and treated with or without pro-inflammatory cytokines (interleukin-1 beta [IL-1 beta], tumor necrosis factor-alpha [TNF-alpha], IL-6) for 2 weeks. After incubation, biotribological tests were performed for 2 hours (alternating 10 minutes test and pause respectively at 39 degrees C, 180 N, 1 Hz, and 2 mm stroke). Before and after testing, the cartilage surface was imaged with a 3-dimensional microscope. During testing, the coefficient of friction (COF) was measured, while gene expression analysis and investigation of metabolic activity of chondrocytes were carried out after testing. Histological sections of the tissue and wear debris from the test fluid were also analyzed. Results After biotribological tests, surface cracks were found in both treated and untreated osteochondral grafts. In treated grafts, the COF increased, and the proteoglycan content in the cartilage tissue decreased, leading to structural changes. Chondrocytes from treated grafts showed increased expression of genes encoding for degradative enzymes, while cartilage-specific gene expression and metabolic activity exhibited no significant differences between treated and untreated groups. No measurable difference in the wear debris in the test fluid was found. Conclusions Treatment of osteochondral grafts with cytokines results in a significantly increased COF, while also leading to significant changes in cartilage proteoglycan content and cartilage matrix compression during biotribological tests.
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Univ Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
MS Ctr ErasMS, Erasmus MC, Univ Med Ctr, Dept Immunol, Rotterdam, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
van Onkelen, R. S.
Gosselink, M. P.
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Maasstad Hosp, Dept Surg, Rotterdam, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
Gosselink, M. P.
van Meurs, M.
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MS Ctr ErasMS, Erasmus MC, Univ Med Ctr, Dept Immunol, Rotterdam, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
van Meurs, M.
Melief, M. J.
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MS Ctr ErasMS, Erasmus MC, Univ Med Ctr, Dept Immunol, Rotterdam, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
Melief, M. J.
Schouten, W. R.
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Univ Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
Schouten, W. R.
Laman, J. D.
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MS Ctr ErasMS, Erasmus MC, Univ Med Ctr, Dept Immunol, Rotterdam, Netherlands
Univ Groningen, Univ Med Ctr Groningen, Dept Neurosci, Groningen, NetherlandsUniv Med Ctr, Erasmus Med Ctr Rotterdam, Dept Surg, Room H 181s Gravendijkwal 230, NL-3015 CE Rotterdam, Netherlands
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Univ Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 2S2, CanadaUniv Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 2S2, Canada
Ho, Emmanuel A.
Piquette-Miller, Micheline
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Univ Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 2S2, CanadaUniv Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, Toronto, ON M5S 2S2, Canada