Expression of type X collagen in young and old C57BI/6 and Balb/c mice. Relation with articular cartilage degeneration

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Abstract

Objective. To investigate whether the development of osteoarthritic lesions in the knee joints of mice is associated with increased immunostaining of type X collagen. Methods. Sections of total knee joints in combination with immunohistochemistry were used to study the distribution of type X collagen in the cartilage of young and old mice of two mouse strains Balb/c and C57Bl/6 known to develop osteoarthritic lesions at different locations. Expression of type X collagen and PTH/PTHrP-receptor mRNA were studied by RT-PCR. Results. Young adult Balb/c and C57Bl/6 mice both expressed type X collagen in the non-calcified cartilage of the tibia-femoral joint. Old mice of both strains had a strongly increased deposition of type X collagen in the patella-femoral but not in the tibia-femoral joint. The locations in the murine knee joints prone to develop osteoarthritis (OA) did not preferentially express increased amounts of type X collagen. Thus whereas increased type X was observed in both strains in the patella-femoral joints only Balb/c mice preferentially developed osteoarthritic lesions in these joints. Also cartilage degeneration was usually seen only in the lateral compartment of the knee joints of C57Bl/6 mice but this was not accompanied by increased type X collagen immunostaining. Increased deposition of type X collagen was not associated with elevated levels of type X collagen mRNA or with decreased levels of PTH/PTHrP-receptor mRNA. Conclusion. Type X collagen expression and spontaneous OA in mice are not necessarily related since OA prone locations in the murine knee joint do not preferentially express type X collagen. © 2001 OsteoArthritis Research Society International.

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van der Kraan, P. M., Stoop, R., Meijers, T. H. M., Poole, A. R., & van den Berg, W. B. (2001). Expression of type X collagen in young and old C57BI/6 and Balb/c mice. Relation with articular cartilage degeneration. Osteoarthritis and Cartilage, 9(2), 92–100. https://doi.org/10.1053/joca.2000.0364

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