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低强度脉冲超声通过Piezo1促进机械力处理的牙周膜细胞的成骨作用。

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

作者信息

Zheng Fu, Wu Tong, Wang Feifei, Li Huazhi, Tang Hongyi, Cui Xinyu, Li Cuiying, Wang Yixiang, Jiang Jiuhui

机构信息

Department of Orthodontics, Peking University School and Hospital of Stomatology, Haidian, Beijing, China.

National Clinical Research Center for Oral Diseases and National Engineering Laboratory for Digital and Material Technology of Stomatology, Haidian, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2024 Apr 17;12:1347406. doi: 10.3389/fbioe.2024.1347406. eCollection 2024.

Abstract

BACKGROUND

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.

METHOD

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.

RESULTS

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.

CONCLUSION

This research unveils that LIPUS promotes the osteogenesis of force-treated PDLCs via downregulating Piezo1.

摘要

背景

低强度脉冲超声(LIPUS)可在正畸治疗期间加速牙齿移动并保持牙齿和骨骼完整性。然而,LIPUS在正畸牙齿移动(OTM)过程中影响组织重塑的机制仍不清楚。牙周膜细胞(PDLCs)在受到机械刺激时对维持牙周组织平衡至关重要。一种著名的机械敏感离子通道Piezo1,可响应机械信号调节细胞功能。本研究旨在阐明Piezo1在LIPUS刺激下力作用的PDLCs成骨反应中的作用。

方法

建立大鼠OTM模型后,使用LIPUS对大鼠进行局部刺激。使用微型计算机断层扫描评估OTM距离和牙槽骨密度,组织学分析包括苏木精和伊红染色、抗酒石酸酸性磷酸酶染色和免疫组织化学染色。GsMTx4和Yoda1分别用于大鼠Piezo1功能抑制和激活实验。我们分离了人PDLCs(hPDLCs),并使用实时定量PCR、蛋白质印迹、碱性磷酸酶和茜素红染色评估LIPUS对力作用的hPDLCs成骨分化的影响。小干扰RNA和Yoda1用于验证Piezo1在此过程中的作用。

结果

LIPUS促进大鼠破骨细胞分化并加速OTM。此外,LIPUS通过下调Piezo1表达减轻压力下的牙槽骨吸收,并增强力作用的PDLCs的成骨作用。随后在大鼠中给予GsMTx4和在hPDLCs中转染siPIEZO1减弱了对压力下成骨分化的抑制作用,而LIPUS的效果部分减轻。Yoda1处理抑制hPDLCs的成骨分化,导致牙周膜中Ⅰ型胶原α1和骨钙素表达降低。然而,给予LIPUS能够抵消这些影响。

结论

本研究揭示LIPUS通过下调Piezo1促进力作用的PDLCs的成骨作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bba/11061374/d786bea03a5c/fbioe-12-1347406-g001.jpg

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