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Piezo1参与牙周膜干细胞的张力驱动成骨分化。

Piezo1 participates in the tension-driven osteogenic differentiation of periodontal ligament stem cells.

作者信息

Du Yugui, Zheng Junyi, Xu Bowen, Peng Chuhan, Yang Kai

机构信息

Department of Orthodontics, School of Stomatology, Capital Medical University, No.9 Fanjiacun Road, Fengtai District, Beijing, 100070, China.

出版信息

BMC Oral Health. 2025 Jul 13;25(1):1155. doi: 10.1186/s12903-025-06427-y.

Abstract

BACKGROUND

Orthodontic tooth movement involves osteogenesis of periodontal ligament stem cells (PDLSCs) in response to tension force. Piezo1 was recognized as a mechanically sensitive channel in 2010, capable of activation by tension force. However, its specific role in tension-induced osteogenic differentiation of PDLSCs remains unclear. This study aims to investigate the involvement Piezo1 in this process.

METHODS

Human PDLSCs were cultured and characterized. Following exposure to half-sine periodic tensile stress (0.1 Hz, 12% elongation) for durations of 0, 1, 3, 6, 9, and 12 h using a Flexcell tension system, phalloidin staining and CCK-8 assays were used to assess the actin cytoskeleton and cell viability, respectively, of PDLSCs. The expression levels of Piezo1 and Ca/calmodulin -dependent protein kinase (CaMKII), as well as CaMKII phosphorylation and calcium influx were evaluated in PDLSCs. The osteogenic factors expression levels (Runt-related transcription factor 2 [Runx2] and alkaline phosphatase [ALP]), together with ALP staining and measurement of ALP activity, were evaluated to characterize osteogenic potential of PDLSCs. Besides, the levels of Yes-associated protein (YAP), and β-catenin as mechanosensitive signaling molecules were also assessed.

RESULTS

After application of the tension force, the PDLSCs exhibited a more extensive spreading morphology, while there were no significant differences in cell viability among the 0, 1, 3, 6, 9, and 12 h groups. PDLSCs exhibited increased osteogenic potential, shown by upregulation of Runx2 and ALP and increased ALP activity after tension force application. Increased expression of Piezo1, accompanied by elevated calcium influx and enhanced CaMKII expression and phosphorylation, was observed in the stretched PDLSCs. The levels of the mechanosensitive signaling molecules YAP and β-catenin also increased in response to the tension force.

CONCLUSIONS

Tension force promotes Piezo1 expression and osteogenic differentiation in PDLSCs. It also enhances calcium influx, CaMKII expression and phosphorylation, and the expression of YAP and β-catenin. Piezo1 participate in the osteogenic differentiation of hPDLSCs under tension force, providing new insights into the molecular mechanisms of osteogenic differentiation in PDLSCs and suggest potential therapeutic targets for modulating bone remodeling during orthodontic tooth movement.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1186/s12903-025-06427-y.

摘要

背景

正畸牙齿移动涉及牙周膜干细胞(PDLSCs)响应张力而发生的成骨作用。Piezo1在2010年被确认为一种机械敏感通道,能够被张力激活。然而,其在PDLSCs张力诱导的成骨分化中的具体作用仍不清楚。本研究旨在探讨Piezo1在这一过程中的作用。

方法

培养并鉴定人PDLSCs。使用Flexcell张力系统,将PDLSCs暴露于半正弦周期性拉伸应力(0.1Hz,12%伸长率)下0、1、3、6、9和12小时,分别用鬼笔环肽染色和CCK-8测定法评估PDLSCs的肌动蛋白细胞骨架和细胞活力。评估PDLSCs中Piezo1和钙/钙调蛋白依赖性蛋白激酶(CaMKII)的表达水平,以及CaMKII磷酸化和钙内流情况。评估成骨因子表达水平( runt相关转录因子2 [Runx2]和碱性磷酸酶[ALP]),以及ALP染色和ALP活性测量,以表征PDLSCs的成骨潜能。此外,还评估了Yes相关蛋白(YAP)和β-连环蛋白作为机械敏感信号分子的水平。

结果

施加张力后,PDLSCs呈现出更广泛的铺展形态,而0、1、3、6、9和12小时组之间的细胞活力没有显著差异。施加张力后,PDLSCs的成骨潜能增加,表现为Runx2和ALP上调以及ALP活性增加。在拉伸的PDLSCs中观察到Piezo1表达增加,同时钙内流增加,CaMKII表达和磷酸化增强。机械敏感信号分子YAP和β-连环蛋白的水平也因张力而增加。

结论

张力促进PDLSCs中Piezo1的表达和成骨分化。它还增强钙内流、CaMKII表达和磷酸化,以及YAP和β-连环蛋白的表达。Piezo1参与了张力作用下hPDLSCs的成骨分化,为PDLSCs成骨分化的分子机制提供了新的见解,并为正畸牙齿移动过程中调节骨重塑提供了潜在的治疗靶点。

补充信息

在线版本包含可在10.1186/s12903-025-06427-y获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd31/12257747/55a1e614a6d2/12903_2025_6427_Fig1_HTML.jpg

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