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.

Abstract

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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