牙周炎
线粒体生物发生
免疫系统
炎症
粒体自噬
线粒体
免疫学
炎症体
线粒体ROS
巨噬细胞
巨噬细胞极化
生物
活性氧
医学
癌症研究
细胞生物学
细胞凋亡
内科学
遗传学
自噬
体外
作者
Yibing Jia,Zili Li,Pengjie Huang,Yan Wang,Bo Yang
标识
DOI:10.3389/fcimb.2025.1634909
摘要
Periodontitis is a global inflammatory oral disease, and plaque-induced host excessive immune response is recognized as a major cause of its pathogenesis. In recent years, the relevance of mitochondrial dysfunction to periodontitis has been increasingly investigated, particularly with respect to macrophages, the key immune cells in the periodontal immune microenvironment. Mitochondrial dysfunction drives macrophage M1 polarization and osteoclast differentiation through mechanisms such as metabolic reprogramming, reactive oxygen species release, abnormal mitophagy, abnormal mitochondrial biogenesis and damaged mitochondrial dynamic. In addition, mitochondrial transfer in the periodontitis setting has been reported in several researches. In this review, we highlight the impact of mitochondrial dysfunction on macrophages in the periodontitis setting and summarize emerging therapeutic strategies for targeting mitochondria in periodontitis, including antioxidants, modulators of metabolic reprogramming, nanomaterials and photodynamic therapy.
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