Patients with rheumatoid arthritis (RA) have lymphatic defects characterized by loss of collecting lymphatic vessel (cLV) contractions of unknown etiology. To elucidate underlying mechanisms, we generated transgenic mice with lymphatic-specific inducible genetics and studied joint-draining lymphatics in zymosan-induced arthritis (ZIA). We crossed novel Efhd1-CreERT2 and Myoc-CreERT2 mice to Ai9 tdTomato (tdT) reporter mice to assess tamoxifen-induced transgene expression via single-cell RNA sequencing, whole-mount immunofluorescent microscopy (WMIFM), and immunohistochemistry. We applied electron and confocal microscopy of popliteal lymphatic vessels (PLVs) to examine α smooth muscle actin positive lymphatic muscle cells, mast cell tryptase-positive mast cells, and CD31-/CD34+ cells. We crossed Efhd1-CreERT2 and Myoc-CreERT2 mice to diphtheria toxin-alphafloxed mice to examine: (1) tamoxifen-induced targeted cell deletion; (2) lymphatic function via near-infrared imaging of injected indocyanine green; and (3) effects on ZIA in the knee via longitudinal ultrasound, micro-computed tomography, and histology. Multimodal microscopy discovered the presence of peri-PLV spindle-shaped cells with elongated cytoplasmic extensions physically integrated into mast cells. Gene expression studies confirmed these cells are consistent with telocytes, and WMIFM demonstrated peri-PLV tdT+ telocyte networks extending from capillaries in the ankle synovium to cLV near the knee. In vivo telocyte depletion decreased lymphatic drainage and exacerbated synovitis and focal erosions in ZIA. Telocyte networks extend from the synovium into mast cells proximal to joint-draining cLVs, and telocyte loss is associated with synovial lymphatic system (SLS) defects and exacerbated joint pathology from inflammatory-erosive arthritis. Thus, SLS telocytes are a novel drug target for RA, and interventions that maintain telocytes (eg, exercise) may improve lymphatic function.
山东省济南市章丘区文博路2号
齐鲁师范学院 genelibs生信实验室
山东省济南市高新区舜华路750号
大学科技园北区F座4单元2楼
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