# Defining subcellular synovial responses in TMJ osteoarthritis onset via mechanical stress and articular disk derangement models

**Authors:** Kazuhiro Shibusaka, Soichiro Negishi, Asuka Terashima, Miki Maemura, Hiroshi Yoshida, Masahiro Hosonuma, Nobuhiro Sakai, Young Kwan Kim, Yutaka Suzuki, Hiroyuki Okada, Fumiko Yano

PMC · DOI: 10.1038/s41368-025-00411-6 · International Journal of Oral Science · 2026-03-12

## TL;DR

This study explores how mechanical stress and joint issues in mice lead to changes in the synovium, offering insights into the early stages of temporomandibular joint osteoarthritis.

## Contribution

The study introduces a novel integrated transcriptomic approach combining subcellular spatial transcriptomics and single-cell RNA sequencing to investigate TMJ-OA onset.

## Key findings

- Molecular alterations in the synovium of the articular disk were identified in response to mechanical and inflammatory stimuli.
- Cell type– and cluster–specific catabolic changes were observed, suggesting roles in TMJ-OA onset.
- The study provides a methodology-oriented resource for understanding TMJ disorders at the molecular level.

## Abstract

Temporomandibular joint osteoarthritis (TMJ-OA), the most common degenerative disease of the TMJ, is influenced by various adaptive, inflammatory, and mechanical stressors. In this study, we describe molecular alterations of the synovium of the articular disk in response to mechanical and inflammatory stimuli. Using an integrated transcriptomic approach combining subcellular spatial transcriptomics and single-cell RNA sequencing in murine models of mechanical stress and articular disk derangement, we characterized synovial changes associated with adipogenesis, fibrosis, and macrophage activation. In addition, cell type–and cluster–specific catabolic changes were observed under these stress conditions, suggesting potential contributions to TMJ-OA onset. These results provide a methodology-oriented resource for investigating the molecular pathology of TMJ disorders and may help guide future studies toward the development of targeted therapeutic strategies.

## Full-text entities

- **Diseases:** TMJ disorders (MESH:D013705), fibrosis (MESH:D005355), degenerative disease (MESH:D019636), inflammatory (MESH:D007249), TMJ (MESH:D013706), articular disk derangement (MESH:D057072)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979832/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979832/full.md

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Source: https://tomesphere.com/paper/PMC12979832