Studying the formation of the zone of calcified cartilage in bovine cartilage explants ex vivo

Journal Article (2026)
Author(s)

Jietao Xu (Erasmus MC, Hangzhou Medical College People’s Hospital)

Andrea Schwab (Erasmus MC, Otto von Guericke University Magdeburg)

Elias Salzer (Erasmus MC)

Nicole Kops (Erasmus MC)

Pieter A.J. Brama (University College Dublin)

Eric Farrell (Erasmus MC)

Gerjo J.V.M. van Osch (Erasmus MC, TU Delft - Mechanical Engineering)

Research Group
Biomaterials & Tissue Biomechanics
DOI related publication
https://doi.org/10.1016/j.ocarto.2026.100743 Final published version
More Info
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Publication Year
2026
Language
English
Research Group
Biomaterials & Tissue Biomechanics
Journal title
Osteoarthritis and Cartilage Open
Issue number
1
Volume number
8
Article number
100743
Downloads counter
76
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Abstract

Objective: The zone of calcified cartilage (ZCC) connects non-calcified articular cartilage to the subchondral bone, acting as transitional layer. Regeneration of this layer is key for cartilage repair but remains a challenge. Knowledge on the formation of this layer during development is limited. This study describes the use of an ex vivo explant culture model to investigate the formation of the ZCC. Design: Explants were harvested from immature bovine metacarpophalangeal joints and cultured in the presence of β-glycerophosphate for 3 weeks as osteochondral explants, full-thickness cartilage or divided in top and bottom cartilage layers. To investigate cell-driven vs matrix-dependent calcification, explants were devitalized. Calcification was analysed using calcium uptake, micro-computed tomography, gene expression analysis, and histological stainings. Results: A distinct area of calcified cartilage formed in the explants ex vivo. This layer showed similar characteristics to the ZCC in mature bovine tissue. Viable chondrocytes in bottom layers actively contributed to cartilage calcification, while calcification in top layers was only present in devitalized top layer explants. Top layers inhibited cartilage calcification in bottom layers and expressed higher levels of FGF18, PTHLH and MGP, while the bottom layers expressed more ALPL, COL10A1 and IHH. Conclusion: We present the first ex vivo model allowing to study and modulate cartilage calcification and the formation of the ZCC. We demonstrated an inherent zone-specific calcification pattern within the cartilage explants. This model allows future studies investigating mechanisms of ZCC formation in cartilage repair procedures, and the role of the top layer in pathological cartilage calcifications and potential interventions.