Abstract

Background:Chondrocytes have been traditionally thought to be responsible for calcium crystal deposits within osteoarthritic knees. Increasing recent experimental evidence suggests that menisci may also play a role. However, the calcifying potential of chondrocytes and meniscal cells derived from same OA patients, and the genes associated with meniscal calcification have never been fully examined.Objective:Examine and compare the calcifying potential of articular chondrocytes and meniscal cells derived from same OA patients and identify the calcium crystal type(s) and selected gene expression in OA menisci.Methods:Chondrocytes and meniscal cells were isolated from articular cartilage and menisci of OA patients undergoing total knee arthroplasty. Chondrocyte- and meniscal cell-mediated calcification was examined using both monolayer and micromass culture-based assays. Crustal types were examined with histological staining. Levels of Type X Collagen, MMP-13, and ANKH in OA menisci were examined using immunohistochemistry.Results:Primary human OA meniscal cells produced calcified deposits at a similar rate compared to OA chondrocytes in-vitro. Histological examinations indicate that both BCP crystals and CPPD crystals are present in the meniscal tissue. Type X collagen, MMP-13, and ANKH were found in human OA menisci and their levels increased with OA severity. In addition, type X collagen was co-localized with calcium crystals.Conclusion:These findings suggest that OA meniscal cells have a similar calcifying potential as OA chondrocytes, supporting a pathogenic role of OA menisci in OA.

Highlights

  • Osteoarthritis (OA) is a degenerative joint disease that is characterized by cartilage degeneration, osteophyte formation, and synovial inflammation [1, 2]

  • Histological examinations indicate that both basic calcium phosphate (BCP) crystals and calcium pyrophosphate dehydrate (CPPD) crystals are present in the meniscal tissue

  • Type X collagen, matrix metalloproteinase (MMP)-13, and ankylosis protein homolog (ANKH) were found in human OA menisci and their levels increased with OA severity

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Summary

Introduction

Osteoarthritis (OA) is a degenerative joint disease that is characterized by cartilage degeneration, osteophyte formation, and synovial inflammation [1, 2]. There is increasing evidence suggesting that the knee meniscus may not be a passive bystander in OA, but may play a much larger part in conjunction with articular cartilage degradation [5, 6]. The formation of calcified articular crystals is a hallmark characteristic commonly associated with advanced OA [7]. These calcified deposits are found throughout the synovial fluid of approximately 65% of OA patients and in all of the cartilage samples obtained from OA patients undergoing knee replacement surgeries [8 - 10]. The calcifying potential of chondrocytes and meniscal cells derived from same OA patients, and the genes associated with meniscal calcification have never been fully examined

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