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强大的机械力通过Piezo1诱导的线粒体钙下调来减缓正畸牙齿移动。

Heavy mechanical force decelerates orthodontic tooth movement via Piezo1-induced mitochondrial calcium down-regulation.

作者信息

Zhu Ye, Meng Xuehuan, Zhai Qiming, Xin Liangjing, Tan Hao, He Xinyi, Li Xiang, Yang Guoyin, Song Jinlin, Zheng Leilei

机构信息

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.

出版信息

Genes Dis. 2024 Sep 15;12(2):101434. doi: 10.1016/j.gendis.2024.101434. eCollection 2025 Mar.

DOI:10.1016/j.gendis.2024.101434
PMID:39759122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11697055/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/34a985c20a18/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/cb72b97e91a2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/e3236db80fc3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/34a985c20a18/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/cb72b97e91a2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/e3236db80fc3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e1d/11697055/34a985c20a18/gr3.jpg

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本文引用的文献

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Force-Loaded Cementocytes Regulate Osteoclastogenesis via S1P/S1PR1/Rac1 Axis.力加载骨细胞通过 S1P/S1PR1/Rac1 轴调节破骨细胞形成。
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Cyclic Stretching Triggers Cell Orientation and Extracellular Matrix Remodeling in a Periodontal Ligament 3D In Vitro Model.
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Role of mechanosensitive ion channel Piezo1 in tension-side orthodontic alveolar bone remodeling in rats.机械敏感离子通道Piezo1在大鼠张力侧正畸牙槽骨重塑中的作用
Arch Oral Biol. 2023 Nov;155:105798. doi: 10.1016/j.archoralbio.2023.105798. Epub 2023 Aug 26.
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Lepr-Expressing PDLSCs Contribute to Periodontal Homeostasis and Respond to Mechanical Force by Piezo1.表达瘦素受体的牙周干细胞有助于牙周组织的稳态平衡,并通过 Piezo1 对机械力产生反应。
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