Jiang Yukun, Guan Yuzhe, Lan Yuanchen, Chen Shuo, Li Tiancheng, Zou Shujuan, Hu Zhiai, Ye Qingsong
State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Center of Regenerative Medicine, Renmin Hospital of Wuhan University, Wuhan, China.
Front Physiol. 2021 Nov 22;12:767136. doi: 10.3389/fphys.2021.767136. eCollection 2021.
Orthodontic tooth movement (OTM) is a process depending on the remodeling of periodontal tissues surrounding the roots. Orthodontic forces trigger the conversion of mechanical stimuli into intercellular chemical signals within periodontal ligament (PDL) cells, activating alveolar bone remodeling, and thereby, initiating OTM. Recently, the mechanosensitive ion channel Piezo1 has been found to play pivotal roles in the different types of human cells by transforming external physical stimuli into intercellular chemical signals. However, the function of Piezo1 during the mechanotransduction process of PDL cells has rarely been reported. Herein, we established a rat OTM model to study the potential role of Piezo1 during the mechanotransduction process of PDL cells and investigate its effects on the tension side of alveolar bone remodeling. A total of 60 male Sprague-Dawley rats were randomly assigned into three groups: the OTM + inhibitor (INH) group, the OTM group, and the control (CON) group. Nickel-titanium orthodontic springs were applied to trigger tooth movement. Mice were sacrificed on days 0, 3, 7, and 14 after orthodontic movement for the radiographic, histological, immunohistochemical, and molecular biological analyses. Our results revealed that the Piezo1 channel was activated by orthodontic force and mainly expressed in the PDL cells during the whole tooth movement period. The activation of the Piezo1 channel was essential for maintaining the rate of orthodontic tooth movement and facilitation of new alveolar bone formation on the tension side. Reduced osteogenesis-associated transcription factors such as Runt-related transcription factor 2 (RUNX2), Osterix (OSX), and receptor activator of nuclear factor-kappa B ligand (RANKL)/osteoprotegerin (OPG) ratio were examined when the function of Piezo1 was inhibited. In summary, Piezo1 plays a critical role in mediating both the osteogenesis and osteoclastic activities on the tension side during OTM.
正畸牙齿移动(OTM)是一个依赖于牙根周围牙周组织重塑的过程。正畸力促使牙周膜(PDL)细胞内机械刺激转化为细胞间化学信号,激活牙槽骨重塑,从而启动OTM。最近,发现机械敏感离子通道Piezo1通过将外部物理刺激转化为细胞间化学信号,在不同类型的人类细胞中发挥关键作用。然而,Piezo1在PDL细胞机械转导过程中的功能鲜有报道。在此,我们建立了大鼠OTM模型,以研究Piezo1在PDL细胞机械转导过程中的潜在作用,并研究其对牙槽骨重塑张力侧的影响。总共60只雄性Sprague-Dawley大鼠被随机分为三组:OTM + 抑制剂(INH)组、OTM组和对照组(CON)。应用镍钛正畸弹簧引发牙齿移动。在正畸移动后的第0、3、7和14天处死小鼠,进行影像学、组织学、免疫组织化学和分子生物学分析。我们的结果显示,Piezo1通道在正畸力作用下被激活,并且在整个牙齿移动期间主要在PDL细胞中表达。Piezo1通道的激活对于维持正畸牙齿移动速率和促进张力侧新牙槽骨形成至关重要。当Piezo1功能受到抑制时,检测到成骨相关转录因子如Runx相关转录因子2(RUNX2)、osterix(OSX)以及核因子-κB受体激活剂配体(RANKL)/骨保护素(OPG)比值降低。总之,Piezo1在OTM期间张力侧的成骨和成破骨活动介导中起关键作用。