Piezo1 reduces inflammation regulatory ability of periodontal ligament cells to decelerate orthodontic tooth movement in response to heavy mechanical force

Author:

Zheng Leilei1,Zhu Ye1,Meng Xuehuan1,Zhai Qiming2,Xin Liangjing1,Tan Hao1,He Xinyi1,Li Xiang1,Yang Guoyin1,Song Jinlin1

Affiliation:

1. Chongqing Medical University

2. Stomatological Hospital of Chongqing Medical University, Chongqing, China

Abstract

Abstract

Periodontal ligament (PDL) cells exhibit immunoregulatory characteristics and are being explored as promising therapeutic candidates for accelerating orthodontic tooth movement (OTM). The impact of light or heavy orthodontic mechanical force (MF) on PDL cellular regulatory ability and the modulation of alveolar bone remodeling during OTM is not yet fully understood. Piezo1, a mechanosensitive ion channel, is essential for mediating the conversion in response to MF stimuli. This study aimed to investigate the influence of light and heavy MF on OTM and the consequent remodeling of alveolar bone by altering the immunoregulatory capabilities of PDL cells through Piezo1 modulation. This research represents the initial exploration of the role of Piezo1 activation by either light or heavy MF in the modulation of mitochondrial calcium concentrations through mitochondria-associated endoplasmic reticulum membranes in PDL cells. The study results have validated that heavy MF-induced deregulation of mitochondrial calcium by Piezo1 leads to a decrease in the release of mitochondrial DNA into the cytoplasm, thereby inhibiting the cGAS-STING pathway activation. Inhibition of the cGAS-STING pathway leads to a decrease in the immunoregulatory capacity of PDL cells during OTM, resulting in reduced osteoclast remodeling and deceleration of rat and sting−/− OTM model. The cumulative findings of this study indicate that manipulating the immunoregulatory ability of PDL cells via Piezo1 could potentially offer an effective strategy to shorten the duration of orthodontic treatment.

Publisher

Research Square Platform LLC

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3