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Published on: July 6, 2022
Rethinking meniscal ossicles as imaging biomarkers for meniscal turnover, overload, and pathology in pre-clinical
Aurea Mohana-Borges1, Laxshmi Veda Avula2, Sanique M South3
1University of California San Diego, CA, USA; Veterans Affairs Medical Center, San Diego, CA, USA.
Objective:
Despite widespread use of mouse osteoarthritis models, meniscal ossicles (MOs), a distinct feature of murine meniscus, remain incompletely characterized. This study aimed to detail MO morphology and bone features in adult mice with and without obesity and post-traumatic osteoarthritis using MRI and micro-CT with histological correlation.
Method:
At 16 weeks, male C57BL/6 mice were assigned to a control-fat diet (CFD) or high-fat diet (HFD). At 36 weeks, right knees underwent sham (CFD) or compression-induced injury (HFD with post-traumatic osteoarthritis; HFD-PTOA) with contralateral knees as internal controls. After the endpoint (40 weeks), MRI and micro-CT assessed MOs for bone marrow (BM) cavities, fragmentation, and bone parameters. Histology evaluated OARSI scores and meniscal surface irregularity.
Results:
Native BM cavities were commonly observed in inner anterior horns, particularly in the lateral meniscus, across groups. Injury was associated with de novo outer-region BM cavities, mainly in the anterior horn of the medial meniscus (AHMM) (CFD vs HFD-PTOA knees; p = 0.018; paired proportion difference = 0.74, 95% CI [-0.27, 0.98]). AHMM fragmentation increased following injury (0% in CFD vs 83% in HFD-PTOA knees; p = 0.015), while posterior horn medial meniscus fragmentation was observed across groups. MO imaging features showed compartment-specific associations with histologic cartilage degeneration and meniscal surface irregularity, mainly in the medial compartment.
Conclusion:
Mineralization and ossification of MOs with marrow formation differ by anatomical region and phenotype. These characteristics are promising imaging biomarkers for assessment of mineral turnover, joint overload and pathology, and the chondro-osteogenic potential of resident meniscal cells.
Insights
Meniscal ossicles (MOs) in mice show distinct bone features and marrow cavities that change with injury and obesity. These imaging characteristics may serve as biomarkers for joint pathology and healing.
Area of Science:
- Orthopedics
- Biomedical Imaging
- Osteoarthritis Research
Background:
- Meniscal ossicles (MOs) are a unique feature of the murine meniscus, but their morphology and bone characteristics are not fully understood.
- Characterizing MOs is crucial for accurately interpreting osteoarthritis (OA) models in mice.
Purpose of the Study:
- To detail the morphology and bone features of meniscal ossicles (MOs) in adult mice.
- To investigate MO changes in mice with obesity and post-traumatic osteoarthritis (PTOA).
- To correlate imaging findings with histological assessments of joint damage.
Main Methods:
- Adult male C57BL/6 mice were fed either a control-fat diet (CFD) or high-fat diet (HFD).
- Post-traumatic osteoarthritis (PTOA) was induced via knee compression in HFD mice; sham surgery in CFD mice.
- MRI and micro-CT were used to assess MOs for bone marrow (BM) cavities and fragmentation; histology evaluated OARSI scores.
Main Results:
- Native bone marrow (BM) cavities were common in inner anterior horns of the meniscus.
- Injury induced new BM cavities in the anterior horn of the medial meniscus (AHMM) and increased AHMM fragmentation.
- MO imaging features correlated with cartilage degeneration and meniscal surface irregularity, particularly in the medial compartment.
Conclusions:
- Meniscal ossicle (MO) mineralization and ossification vary by anatomical region and diet/injury phenotype.
- MO imaging features show potential as biomarkers for assessing joint overload, pathology, and the chondro-osteogenic capacity of meniscal cells.
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