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Standardized Histomorphometric Evaluation of Osteoarthritis in a Surgical Mouse Model
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Relations between Structure/Composition and Mechanics in Osteoarthritic Regenerated Articular Tissue: A Machine
Matteo Berni1, Francesca Veronesi2, Milena Fini3
1Medical Technology Laboratory, IRCCS Istituto Ortopedico Rizzoli, Via Di Barbiano 1/10, 40136 Bologna, Italy.
International Journal of Molecular Sciences
|September 9, 2023
Summary
Mesenchymal stem cell treatments for osteoarthritis (OA) show potential in improving cartilage viscoelasticity. Stromal vascular fraction (SVF) was the only treatment to limit OA
Area of Science:
- Orthopedics
- Regenerative Medicine
- Biomaterials Science
Background:
- Osteoarthritis (OA) is a degenerative joint disease characterized by cartilage breakdown and loss of viscoelastic properties.
- Orthobiologics, including mesenchymal stem cells (MSCs), are being investigated for OA treatment.
- Understanding the relationship between tissue structure, composition, and cartilage function is crucial for developing effective OA therapies.
Purpose of the Study:
- To investigate the relationship between articular tissue structure/composition and cartilage viscoelasticity in a large animal model of early osteoarthritis (OA).
- To evaluate the efficacy of different mesenchymal stem cell preparations (adipose-derived mesenchymal stem cells (ADSCs), stromal vascular fraction (SVF), and amniotic endothelial cells (AECs)) in treating OA.
- To identify key biomarkers and structural parameters influencing cartilage viscoelasticity in OA.
Main Methods:
- A large animal model of induced knee OA in 24 sheep was used.
- Sheep were treated with ADSCs, SVF, or AECs and euthanized at 3 or 6 months post-treatment.
- Analyses included synovial fluid biochemistry, cartilage histology/immunohistochemistry/histomorphometry, and cartilage viscoelasticity measurements.
- Machine learning models (VSURF and XGB) were employed for variable selection and interpretation.
Main Results:
- A correlation was found between cartilage elastic modulus and cartilage thickness (CT), synovial fluid interleukin 6 (IL6), and prostaglandin E2 (PGE2).
- Cartilage relaxation time was associated with CT and PGE2.
- Stromal vascular fraction (SVF) treatment demonstrated a protective effect against the detrimental impact of OA on cartilage viscoelastic properties.
Conclusions:
- This study highlights potential relationships between specific biochemical markers (IL6, PGE2), structural parameters (CT), and cartilage viscoelasticity in OA.
- SVF emerged as a promising orthobiologic treatment, mitigating OA-induced viscoelastic deterioration.
- Findings provide a basis for future research into advanced regenerative targets for OA treatment.
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