Zhu Ye, Meng Xuehuan, Zhai Qiming, Xin Liangjing, Tan Hao, He Xinyi, Li Xiang, Yang Guoyin, Song Jinlin, Zheng Leilei
College of Stomatology, Chongqing Medical University, Chongqing Key Laboratory of Oral Diseases, Chongqing Municipal Key Laboratory of Oral Biomedical Engineering of Higher Education, Chongqing 401147, China.
Genes Dis. 2024 Sep 15;12(2):101434. doi: 10.1016/j.gendis.2024.101434. eCollection 2025 Mar.
Orthodontic tooth movement (OTM) depends on periodontal ligament cells (PDLCs), which sense biomechanical stimuli and initiate alveolar bone remodeling. Light (optimal) forces accelerate OTM, whereas heavy forces decelerate it. However, the mechanisms by which PDLCs sense biomechanical stimuli and affect osteoclastic activities under different mechanical forces (MFs) remain unclear. This study demonstrates that mechanosensitive ion channel Piezo1-mediated Ca signal conversion is crucial for sensing and delivering biomechanical signals in PDLCs under heavy-force conditions. Heavy MF up-regulated Piezo1 in PDLCs, reducing mitochondrial Ca influx by inhibiting ITPR3 expression in mitochondria-associated membranes. Decreased mitochondrial calcium uptake led to reduced cytoplasmic release of mitochondrial DNA and inhibited the activation of the cGAS‒STING signaling cascade, subsequently inhibiting monocyte-to-osteoclast differentiation. Inhibition of Piezo1 or up-regulation of STING expression under heavy MF conditions significantly increased osteoclast activity and accelerated OTM. These findings suggest that heavy MF-induced Piezo1 expression in PDLCs is closely related to the control of osteoclast activity during OTM and plays an essential role in alveolar bone remodeling. This mechanism may be a potential therapeutic target for accelerating OTM.
正畸牙齿移动(OTM)依赖于牙周膜细胞(PDLCs),这些细胞感知生物力学刺激并启动牙槽骨重塑。轻(最佳)力可加速OTM,而重力则使其减速。然而,PDLCs在不同机械力(MFs)作用下感知生物力学刺激并影响破骨细胞活性的机制仍不清楚。本研究表明,机械敏感离子通道Piezo1介导的Ca信号转换对于在重力条件下PDLCs中感知和传递生物力学信号至关重要。重力MF上调了PDLCs中的Piezo1,通过抑制线粒体相关膜中ITPR3的表达减少线粒体Ca内流。线粒体钙摄取减少导致线粒体DNA的细胞质释放减少,并抑制cGAS-STING信号级联的激活,随后抑制单核细胞向破骨细胞的分化。在重力MF条件下抑制Piezo1或上调STING表达可显著增加破骨细胞活性并加速OTM。这些发现表明,重力MF诱导的PDLCs中Piezo1表达与OTM过程中破骨细胞活性的控制密切相关,并在牙槽骨重塑中起重要作用。这一机制可能是加速OTM的潜在治疗靶点。