Unraveling The Mechanism Behind Orthodontic Tooth Movement

Heavy mechanical force (MF)-activated Piezo1 decelerates orthodontic tooth movement (OTM) in vivo.

Heavy mechanical force (MF) conditions activate Piezo1-inhibited ITPR3 in periodontal ligament stem cells.

Heavy mechanical force (MF)-activated Piezo1 down-regulates [Ca2+]m levels by inhibiting ITPR3 in mitochondria-associated membranes.

SHANNON, CLARE, IRELAND, March 1, 2025 /EINPresswire / -- A new study in Genes & Diseases has revealed that heavy mechanical force can decelerate orthodontic tooth movement (OTM) by altering the way periodontal ligament cells (PDLCs) respond to stress. The authors of this article have identified the key role of Piezo1, a mechanosensitive ion channel, in controlling this process by regulating mitochondrial calcium levels, ultimately affecting bone remodeling.

Orthodontic tooth movement is driven by the body's response to mechanical forces applied during treatment. While light mechanical forces are known to optimize movement by promoting bone remodeling, excessive force has been observed to slow down the process. This study explains the cellular mechanisms behind this phenomenon and provides potential therapeutic targets to improve treatment efficiency.

It was discovered that heavy force upregulates Piezo1 expression in periodontal ligament cells, disrupting mitochondrial calcium homeostasis. This occurs through the inhibition of ITPR3, a key calcium transporter in mitochondria-associated membranes (MAMs). The resulting reduction in mitochondrial calcium uptake leads to lower cytoplasmic mitochondrial DNA release, ultimately suppressing the cGAS–STING signaling pathway-a crucial regulator of osteoclast activity. Since osteoclasts are responsible for breaking down bone tissue to allow tooth movement, their suppression under heavy mechanical force leads to slower tooth repositioning.

In experiments involving both animal models and in vitro studies, the authors found that blocking Piezo1 activity or enhancing STING signaling could restore osteoclast function and accelerate tooth movement under heavy force conditions. These findings suggest that targeting Piezo1 or its downstream pathways could help optimize orthodontic treatment strategies, allowing for more predictable and efficient tooth realignment.

This research not only enhances understanding of biomechanical force transduction in orthodontics but also opens new avenues for developing pharmacological interventions that could improve treatment outcomes. By fine-tuning the balance of mechanical force and cellular signaling, clinicians may be able to personalize orthodontic treatments for faster and safer results.

The findings mark a significant step forward in orthodontic science, shedding light on how force application impacts cellular behavior and offering a roadmap for future innovations in tooth movement acceleration strategies.

Funding Information:
Natural Science Foundation of China 82471016
Natural Science Foundation of China 81470772
Chongqing Talent Program: Innovative Leading Talents CQYC20210303384
Chongqing Medical Scientific Research Project (China) cstc2020jcyj-msxmX0307
Youth Innovation in Future Medicine (Chongqing Medical University) W0033

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Genes & Diseases publishes rigorously peer-reviewed and high quality original articles and authoritative reviews that focus on the molecular bases of human diseases. Emphasis is placed on hypothesis-driven, mechanistic studies relevant to pathogenesis and/or experimental therapeutics of human diseases. The journal has worldwide authorship, and a broad scope in basic and translational biomedical research of molecular biology, molecular genetics, and cell biology, including but not limited to cell proliferation and apoptosis, signal transduction, stem cell biology, developmental biology, gene regulation and epigenetics, cancer biology, immunity and infection, neuroscience, disease-specific animal models, gene and cell-based therapies, and regenerative medicine.

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Reference
Ye Zhu, Xuehuan Meng, Qiming Zhai, Liangjing Xin, Hao Tan, Xinyi He, Xiang Li, Guoyin Yang, Jinlin Song, Leilei Zheng, Heavy mechanical force decelerates orthodontic tooth movement via Piezo1-induced mitochondrial calcium down-regulation, Genes & Diseases, Volume 12, Issue 2, 2025, 101434,

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