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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 2

Painful behaviors and neuroimmune response in CFA intra-articular injection mice.

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Painful behaviors and neuroimmune response in CFA intra-articular inject...
(A) Diagram of von Frey filament test. (B) Diagram of bite force measurement. (C) Quantification of head withdrawal threshold measurement at different time points after CFA injection. N = 7 mice (control), n = 10 mice (CFA). (D) Quantification of relative bite force values at different time points. N = 7 mice (control), n = 10 mice (CFA). (E) Confocal imaging of tdTomato TG section after retrograde tracer Fast Blue in the TMJ. V1, V2, V3 represent ophthalmic nerve (V1), maxillary nerve (V2), and mandibular nerve (V3). Original magnification, 4× for original image; 20× for zoomed-in image. (F) Immunofluorescence staining of CGRP (green) and Iba1 (red) in V3 section of TG. Scale bar 100 μm. (G and H) Quantification of the percentage of CGRP+ neurons and the percentage of Iba1+ area fraction in the V3 of TG. N = 3 mice. (I) Immunofluorescence staining of spinal trigeminal nucleus caudalis (SpVC) using antibodies against microglia marker Iba1 (red) and microglial activation marker CD68 (green). Scale bars: 100 μm. (J) Quantification of the total length of processes per microglia. N ≥ 3 mice. (K) Quantification of Iba1+ cells in SpVC area. N = 3. (L) Quantification of the number of primary processes per microglia. N ≥ 3 mice. All data are represented as mean ± SEM calculated by Student’s t test. n ≥ 3 mice, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001. TG, trigeminal ganglion; CGRP, calcitonin gene-related peptide; Iba1, ionized calcium-binding adapter molecule 1.

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