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牙周膜干细胞产生的力诱导的高应变在牙齿移动过程中改变破骨细胞活性。

Force-Induced HS by PDLSCs Modifies Osteoclastic Activity during Tooth Movement.

作者信息

Liu F, Wen F, He D, Liu D, Yang R, Wang X, Yan Y, Liu Y, Kou X, Zhou Y

机构信息

1 Department of Orthodontics, Peking University School and Hospital of Stomatology, Haidian District, Beijing, P.R. China.

2 Center for Craniofacial Stem Cell Research and Regeneration, Peking University School and Hospital of Stomatology, Haidian District, Beijing, P.R. China.

出版信息

J Dent Res. 2017 Jun;96(6):694-702. doi: 10.1177/0022034517690388. Epub 2017 Feb 6.

Abstract

Hydrogen sulfide (HS), a gasotransmitter, has been recently linked to mesenchymal stem cell (MSC) function and bone homeostasis. Periodontal ligament stem cells (PDLSCs) are the main MSCs in PDL, which respond to mechanical force to induce physiological activities during orthodontic tooth movement (OTM). However, it is unknown whether mechanical force might induce endogenous HS production by PDLSCs to regulate alveolar bone homeostasis. Here, we used a mouse OTM model to demonstrate that orthodontic force-induced endogenous HS production in PDL tissue was associated with macrophage accumulation and osteoclastic activity in alveolar bone. Then, we showed that mechanical force application induced cystathionine β-synthase (CBS) expression and endogenous HS production by PDLSCs. Moreover, blocking endogenous HS or systemically increasing HS levels could decrease or enhance force-induced osteoclastic activities to control tooth movement. We further revealed how force-induced HS production by PDLSCs contributed to the secretion of monocyte chemoattractant protein-1 (MCP-1) and the expression of receptor activator of nuclear factor-κB ligand/osteoprotegerin (RANKL/OPG) system by PDLSCs. The secretion and expression of these factors controlled macrophage migration and osteoclast differentiation. This study demonstrated that PDLSCs produced HS to respond to and transduce force signals. Force-induced gasotransmitter HS production in PDLSCs therefore regulated osteoclastic activities in alveolar bone and controlled the OTM process through the MCP-1 secretion and RANKL/OPG system.

摘要

硫化氢(HS)作为一种气体信号分子,最近被认为与间充质干细胞(MSC)功能及骨稳态有关。牙周膜干细胞(PDLSCs)是牙周膜中的主要间充质干细胞,在正畸牙移动(OTM)过程中,它们对机械力作出反应以诱导生理活动。然而,机械力是否会诱导PDLSCs产生内源性HS以调节牙槽骨稳态尚不清楚。在此,我们使用小鼠OTM模型来证明正畸力诱导的PDL组织内源性HS产生与牙槽骨中的巨噬细胞积聚和破骨细胞活性有关。然后,我们表明施加机械力可诱导PDLSCs表达胱硫醚β-合酶(CBS)并产生内源性HS。此外,阻断内源性HS或全身性增加HS水平可降低或增强力诱导的破骨细胞活性以控制牙齿移动。我们进一步揭示了PDLSCs力诱导的HS产生如何促进单核细胞趋化蛋白-1(MCP-1)的分泌以及PDLSCs中核因子κB受体活化因子配体/骨保护素(RANKL/OPG)系统的表达。这些因子的分泌和表达控制巨噬细胞迁移和破骨细胞分化。本研究表明,PDLSCs产生HS以响应和转导力信号。因此,PDLSCs中力诱导的气体信号分子HS产生通过MCP-1分泌和RANKL/OPG系统调节牙槽骨中的破骨细胞活性并控制OTM过程。

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