Low-intensity pulsed ultrasound promotes the osteogenesis of mechanical force-treated periodontal ligament cells via Piezo1

Low-intensity pulsed ultrasound (LIPUS) can accelerate tooth movement and preserve tooth and bone integrity during orthodontic treatment. However, the mechanisms by which LIPUS affects tissue remodeling during orthodontic tooth movement (OTM) remain unclear. Periodontal ligament cells (PDLCs) are pi...

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Published inFrontiers in bioengineering and biotechnology Vol. 12; p. 1347406
Main Authors Zheng, Fu, Wu, Tong, Wang, Feifei, Li, Huazhi, Tang, Hongyi, Cui, Xinyu, Li, Cuiying, Wang, Yixiang, Jiang, Jiuhui
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 17.04.2024
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Summary:Low-intensity pulsed ultrasound (LIPUS) can accelerate tooth movement and preserve tooth and bone integrity during orthodontic treatment. However, the mechanisms by which LIPUS affects tissue remodeling during orthodontic tooth movement (OTM) remain unclear. Periodontal ligament cells (PDLCs) are pivotal in maintaining periodontal tissue equilibrium when subjected to mechanical stimuli. One notable mechano-sensitive ion channel, Piezo1, can modulate cellular function in response to mechanical cues. This study aimed to elucidate the involvement of Piezo1 in the osteogenic response of force-treated PDLCs when stimulated by LIPUS. After establishing rat OTM models, LIPUS was used to stimulate rats locally. OTM distance and alveolar bone density were assessed using micro-computed tomography, and histological analyses included hematoxylin and eosin staining, tartrate-resistant acid phosphatase staining and immunohistochemical staining. GsMTx4 and Yoda1 were respectively utilized for Piezo1 functional inhibition and activation experiments in rats. We isolated human PDLCs (hPDLCs) and evaluated the effects of LIPUS on the osteogenic differentiation of force-treated hPDLCs using real-time quantitative PCR, Western blot, alkaline phosphatase and alizarin red staining. Small interfering RNA and Yoda1 were employed to validate the role of Piezo1 in this process. LIPUS promoted osteoclast differentiation and accelerated OTM in rats. Furthermore, LIPUS alleviated alveolar bone resorption under pressure and enhanced osteogenesis of force-treated PDLCs both and by downregulating Piezo1 expression. Subsequent administration of GsMTx4 in rats and siPIEZO1 transfection in hPDLCs attenuated the inhibitory effect on osteogenic differentiation under pressure, whereas LIPUS efficacy was partially mitigated. Yoda1 treatment inhibited osteogenic differentiation of hPDLCs, resulting in reduced expression of Collagen Ⅰα1 and osteocalcin in the periodontal ligament. However, LIPUS administration was able to counteract these effects. This research unveils that LIPUS promotes the osteogenesis of force-treated PDLCs via downregulating Piezo1.
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Reviewed by: Fang Hua, Wuhan University, China
Agnes Schröder, University Hospital Regensburg, Germany
These authors have contributed equally to this work and share senior authorship
Jose Mauro Granjeiro, Quality and Technology, Brazil
Edited by: Caroline Curtin, Royal College of Surgeons in Ireland, Ireland
ORCID: Yixiang Wang, orcid.org/0000-0001-5291-9826; Jiuhui Jiang, orcid.org/0000-0003-4881-5949
ISSN:2296-4185
2296-4185
DOI:10.3389/fbioe.2024.1347406