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Mapping cell diversity and dynamics in inflammatory temporomandibular joint osteoarthritis with pain at single-cell resolution
Supawadee Jariyasakulroj, … , Pao-Fen Ko, Jian-Fu Chen
Supawadee Jariyasakulroj, … , Pao-Fen Ko, Jian-Fu Chen
Published February 10, 2025
Citation Information: JCI Insight. 2025;10(3):e184379. https://doi.org/10.1172/jci.insight.184379.
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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 7

Immune cell heterogeneity and increased inflammatory response in CFA TMJ.

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Immune cell heterogeneity and increased inflammatory response in CFA TMJ...
(A) UMAP plot of immune cell clusters in adult mouse CFA TMJ. (B and D) Dot plot and heatmap of signature genes in different immune cell clusters including monocyte, osteoclast, and macrophage. (C) Feature plots showing the expression of indicated cell type marker genes that are overlaid on the UMAP plot. (E) UMAP plot for both control and CFA with the major cell types. Black arrowheads indicate the most upregulated cell types, including neutrophils and macrophages, in CFA TMJ. (F) Confocal imaging of sagittal TMJ sections stained with antibodies against Iba1 (white). DAPI stains nuclei (blue). Scale bar: 100 μm. (G and H) Quantification of the area fraction of Iba1+ macrophages (surrounding TMJ) and Ly6b+ neutrophils (anterior part of surrounding TMJ). N = 3–4 mice. (I) Schematic diagram of expanded Iba1+ macrophages (black) and Ly6b+ neutrophils (red) in CFA TMJ compared with control. (J and K) RNAscope of IL-1β (red) and immunofluorescence staining of Ly6b (white) and Iba1 (green) in different regions surrounding TMJ. DAPI stains nuclei (blue). Images in K (20× objective) are enlargements of boxed regions in J (4× objective). Scale bars: 100 μm. (L–N) Quantification of the area fraction of IL-1β+Ly6b+ and IL-1β+Iba1+ cells in the anterior, posterior, and superior regions of TMJ. N = 3–5 mice. All data are represented as mean ± SEM. Student’s t test. N = 3–5 mice, *P < 0.05, **P < 0.01, ***P < 0.001.

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