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Mapping cell diversity and dynamics in inflammatory temporomandibular joint osteoarthritis with pain at single-cell resolution
Supawadee Jariyasakulroj, Yang Shu, Ziying Lin, Jingyi Chen, Qing Chang, Pao-Fen Ko, Jian-Fu Chen
Supawadee Jariyasakulroj, Yang Shu, Ziying Lin, Jingyi Chen, Qing Chang, Pao-Fen Ko, Jian-Fu Chen
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Research Article Cell biology Inflammation

Mapping cell diversity and dynamics in inflammatory temporomandibular joint osteoarthritis with pain at single-cell resolution

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Abstract

Temporomandibular joint (TMJ) osteoarthritis with pain is a highly prevalent disorder affecting patients’ quality of life. A comprehensive understanding of cell type diversity and its dynamics in painful TMJ osteoarthritis (TMJOA) is lacking. Here, we utilized an inflammatory TMJOA mouse model via intra-articular injection of CFA. TMJOA mice exhibited cartilage remodeling, bone loss, synovitis, increased osteoarthritis (OA) score, and orofacial pain, recapitulating hallmark symptoms in patients. Single-cell transcriptomic profiling of the TMJ was performed in conjunction with mouse genetic labeling, tissue clearing, light sheet and confocal 3D imaging, multiplex RNAscope, and immunodetection. We visualized, reconstructed, and analyzed the distribution and density of nociceptive innervation of TMJ at single-axon levels. We systematically mapped the heterogeneity and anatomical position of blood endothelial cells, synovial fibroblasts, and immune cells, including Cx3cr1-positive barrier macrophages. Importantly, TMJOA mice exhibited enhanced neurovascular coupling, sublining fibroblast hyperplasia, inflammatory immune cell expansion, disrupted signaling-dependent cell-cell interaction, and a breakdown of the sandwich-like organization consisting of synovial barrier macrophages and fibroblasts. By utilizing a mouse model with combined TMJ pain history and OA, we reveal the cellular diversity, anatomical structure, and cell dynamics of the TMJ at single-cell resolution, which facilitate our understanding and potential targeting of TMJOA.

Authors

Supawadee Jariyasakulroj, Yang Shu, Ziying Lin, Jingyi Chen, Qing Chang, Pao-Fen Ko, Jian-Fu Chen

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Figure 6

Synovial fibroblast heterogeneity and anatomical locations in control and CFA TMJ.

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Synovial fibroblast heterogeneity and anatomical locations in control an...
(A) UMAP plot of fibroblast cell clusters in adult mouse TMJ. (B and C) Dot plot and heatmap of signature genes in different fibroblast cell clusters including lining, perivascular, and sublining fibroblasts. (D and E) Confocal imaging of TMJ sagittal sections after RNAscope staining of Thy1 (green) and Prg4 (red). DAPI stains nuclei (blue). Images in E (20× objective) are enlargements of boxed TMJ regions in D (4× objective). Scale bars: 100 μm. (F–H) Quantification of the area fraction of Thy1+ sublining fibroblast and Prg4+ lining fibroblast area fraction in the TMJ area. N ≥ 3 mice. (I) Feature plots showing the expression of indicated genes that are overlaid on the UMAP plot. (J) Schematic overview of expanded Thy1+ sublining fibroblasts and reduced Prg4+ expression in synovial lining fibroblasts in CFA-induced TMJOA with pain. All data are represented as mean ± SEM. Student’s t test, N ≥ 3 mice. *P < 0.05, **P < 0.01, ***P < 0.001. Prg4, proteoglycan 4.

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