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Updated: Dec 23, 2025

Culture of Murine Embryonic Metatarsals: A Physiological Model of Endochondral Ossification
Published on: December 3, 2016
Maturity-dependent cartilage cell plasticity and sensitivity to external perturbation
Shannon K Walsh1, Stephanie E Schneider2, Laura A Amundson3
1Comparative Biomedical Sciences Program, University of Wisconsin-Madison, Madison, WI, USA.
Articular cartilage shows changing cell markers and gene expression with age. Younger cartilage is more adaptable, while mature cartilage loses plasticity, impacting regeneration and osteoarthritis risk.
Area of Science:
- Biochemistry
- Cell Biology
- Orthopedics
Background:
- Articular cartilage changes biologically and morphologically during maturation.
- Osteoarthritis prevalence in aging populations suggests maturation impacts cartilage degradation and regeneration.
- The precise mechanisms of age-related cartilage changes are not fully understood.
Purpose of the Study:
- To characterize the cellular and genetic profile of articular cartilage.
- To assess cartilage biological plasticity in response to mechanical and culture stimuli.
- To investigate these changes as a function of animal maturity.
Main Methods:
- Porcine articular cartilage explants from immature, adolescent, and mature animals were used.
- Explants were subjected to mechanical loading or served as controls.
- Flow cytometry, qPCR, and histology were employed to analyze progenitor cell markers, matrix synthesis genes, and tissue morphology.
Main Results:
- Chondroprogenitor marker expression (CD105, CD29) decreased with maturity, while CD44 increased.
- Matrix synthesis genes were generally upregulated in mature cartilage; adolescent cartilage showed lowest expression.
- Younger cartilage exhibited greater plasticity to mechanical loading and culture time, with distinct profiles across maturity.
Conclusions:
- Cartilage exhibits differential, nonlinear expression of chondroprogenitor markers and matrix genes with maturity.
- Aging leads to a loss of biological plasticity in articular cartilage.
- These findings suggest implications for age-related regenerative capacity decline and osteoarthritis progression.
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