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ABSTRACT: Background
Efficient clearance of necrotic marrow is essential for repair after epiphyseal ischemia, yet the tissue-level spatiotemporal evolution of this process and its immunoregulatory mechanisms remain incompletely defined.Methods
Using a refined juvenile ischemic osteonecrosis (JIO) model of the murine distal femoral epiphysis-with medial plus lateral approaches guided by mapped vascular entry points-we fully interrupted epiphyseal perfusion and harvested tissue at postoperative days 1-28. Coronal sections along the vascular entry axis underwent H&E/TUNEL and zonal IHC/IF (Ly6G, myeloperoxidase (MPO), F4/80, EMCN, iNOS, CD206). An in-vitro assay tested whether recombinant MPO (1 μg/mL) modulates LPS + IFN-γ-induced M1 polarization in RAW264.7 cells.Results
We c
SUBMITTER: Zhao M
PROVIDER: S-EPMC12750857 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature