巨噬细胞极化
关节炎
滑膜炎
医学
炎性关节炎
压电1
滑膜
炎症
免疫学
软骨细胞
免疫系统
巨噬细胞
软骨
病理
癌症研究
内科学
化学
体外
解剖
受体
生物化学
离子通道
机械敏感通道
作者
Lihang Shen,Ruiliu Li,Yifei Wang,Shuo Chen,Yang He
出处
期刊:Oral Diseases
[Wiley]
日期:2025-08-16
卷期号:31 (11): 3126-3139
被引量:2
摘要
OBJECTIVES: Synovial macrophages are pivotal regulators of the immune response in temporomandibular joint (TMJ) arthritis. This study investigates Piezo's regulatory effects on macrophage polarization and function in TMJ arthritis progression. METHODS: A complete Freund's adjuvant (CFA) induced TMJ arthritis model was established in C57BL/6JNifdc mice, with saline as control. The treated group received Piezo1 inhibitor GsMTx4. Synovitis severity, cartilage degradation, and bone resorption were evaluated by morphological and radiological analyses. Macrophage infiltration, Piezo1, and inflammatory cytokines were analyzed via immunohistochemistry and immunofluorescence. WB and qPCR were used to study signaling pathways in bone marrow-derived macrophages (BMDMs) treated with Piezo1 siRNA, GsMTx4, and Yoda1. RESULTS: macrophages. In vitro studies demonstrated that Piezo1 activates pro-inflammatory macrophages through the NF-κB pathway, whereas it suppresses anti-inflammatory macrophage polarization by inhibiting the STAT6 pathway. GsMTx4 treatment notably alleviated arthritis symptoms. CONCLUSIONS: The disturbed balance between pro-inflammatory and anti-inflammatory macrophages in synovitis may contribute to TMJ arthritis progression. Piezo1 modulates macrophage transcriptional regulation and polarization, influencing immune responses within the synovial environment and offering a potential therapeutic target for TMJ arthritis.
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