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Updated: Feb 18, 2026

Analysis and Imaging of Osteocytes
Published on: November 29, 2024
Imaging mass cytometry unveils functional and spatial remodeling of peri-lesional cells in jaw osteonecrosis
Jiazheng Cai1, Ying Xue2, Stian Tornaas3
1Department of Medical Biology, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway.
Abstract:
Medication-related osteonecrosis of the jaw (MRONJ) is a severe complication associated with antiresorptive therapy, characterized by compromised bone and soft tissue integrity. However, the underlying tissue-level mechanisms remain poorly understood. To uncover cell functions and spatial organization surrounding ONJ lesions, imaging mass cytometry is used to profile lesions at single-cell resolution across epithelial, stromal, and vascular regions. Widespread immune infiltration is observed, with regulatory T cells, M2-like macrophages, exhausted T cells, and natural killer cells shifting from dispersed to clustered spatial patterns, indicating altered immune organization. Epithelial regions show reduced epithelial marker expression and disrupted architecture despite elevated proliferation-related markers, while fibroblasts and endothelial cells display signs of activation. Functional profiling reveals concurrent proliferative, apoptotic, and stress-associated signatures across multiple cell populations. This comprehensive spatial and functional atlas provides insights into the pathophysiology of MRONJ and may inform future therapeutic strategies aimed at restoring tissue homeostasis and promoting effective healing.
Insights
Medication-related osteonecrosis of the jaw (MRONJ) involves altered immune cell organization and tissue dysfunction. This study reveals key cellular changes in MRONJ lesions, offering insights for new therapeutic approaches.
Area of Science:
- Biomedical Science
- Pathophysiology
- Immunology
Background:
- Medication-related osteonecrosis of the jaw (MRONJ) is a serious complication of antiresorptive therapy.
- The precise tissue-level mechanisms driving MRONJ remain unclear.
Purpose of the Study:
- To investigate the cellular functions and spatial organization within MRONJ lesions.
- To provide a detailed spatial and functional atlas of the affected tissues.
Main Methods:
- Utilized imaging mass cytometry to profile MRONJ lesions at single-cell resolution.
- Analyzed epithelial, stromal, and vascular regions within the lesions.
Main Results:
- Observed significant immune cell infiltration, including regulatory T cells, M2-like macrophages, exhausted T cells, and natural killer cells.
- Identified shifts in immune cell spatial patterns from dispersed to clustered arrangements.
- Detected disrupted epithelial architecture, activated fibroblasts and endothelial cells, and concurrent proliferative, apoptotic, and stress signatures across cell types.
Conclusions:
- The study provides a comprehensive spatial and functional understanding of MRONJ pathophysiology.
- Findings suggest potential therapeutic targets for restoring tissue homeostasis and promoting healing in MRONJ patients.
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