Fu Hai-Di, Wang Bei-Ke, Wan Zi-Qiu, Lin Heng, Chang Mao-Lin, Han Guang-Li
State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory for Oral Biomedicine of Ministry of Education (KLOBM), School and Hospital of Stomatology, Wuhan University, 237 Luoyu Road, Wuhan, 430079, China.
Department of Orthodontics, School and Hospital of Stomatology, Wuhan University, Wuhan, China.
J Mol Histol. 2016 Oct;47(5):455-66. doi: 10.1007/s10735-016-9687-y. Epub 2016 Jul 25.
Orthodontic tooth movement (OTM) is associated with bone remodeling mediated by orthodontic mechanical loading. Increasing studies reported that Wnt signaling played crucial roles in mechanical stimuli induced bone remodeling. However, little is known about the involvement of Wnt signaling in orthodontic force-induced bone formation during OTM. In virtue of the OTM mice model as we previously reported, where new bone formation was determined by micro-CT and immunoreactivity of osteocalcin and osterix, we explored the activation of Wnt signaling pathway during OTM. Our results proved the nuclei translocation of β-catenin, suggesting the activation of canonical Wnt signaling pathway in the periodontal ligament cells (PDLCs) near the alveolar bone at the tension site (TS). Moreover, the immunoreactivity of Wnt5a, but not Wnt3a in PDLCs indicated the activation of canonical Wnt pathway might be mediated by Wnt5a, but not Wnt3a as in most cases. The co-location of Wnt5a and β-catenin that was evidenced by double labeling immunofluorescence staining further supported the hypothesis. In addition, the high expression of FZD4 and LRP5 in PDLCs at TS of periodontium suggested that the activation of Wnt signaling pathway was mediated by these receptors. The negligible expression of ROR2 also indicated that canonical but not non-canonical Wnt signaling pathway was activated by Wnt5a, since previous studies demonstrated that the activation of canonical/non-canonical Wnt signaling pathway was largely dependent on the receptors. In summary, we here reported that Wnt5a mediated activation of canonical Wnt signaling pathway might contribute to the orthodontic force induced bone remodeling.
正畸牙齿移动(OTM)与正畸机械负荷介导的骨重塑相关。越来越多的研究报道,Wnt信号在机械刺激诱导的骨重塑中起关键作用。然而,关于Wnt信号在OTM过程中正畸力诱导的骨形成中的作用知之甚少。借助我们之前报道的OTM小鼠模型,通过显微CT以及骨钙素和osterix的免疫反应性来确定新骨形成,我们探索了OTM过程中Wnt信号通路的激活情况。我们的结果证实了β-连环蛋白的核转位,表明在张力部位(TS)牙槽骨附近的牙周膜细胞(PDLCs)中经典Wnt信号通路被激活。此外,PDLCs中Wnt5a而非Wnt3a的免疫反应性表明,经典Wnt通路的激活可能由Wnt5a介导,而非如大多数情况那样由Wnt3a介导。双重免疫荧光染色证明的Wnt5a与β-连环蛋白的共定位进一步支持了这一假设。此外,牙周膜TS处PDLCs中FZD4和LRP5的高表达表明Wnt信号通路的激活是由这些受体介导的。ROR2的表达可忽略不计也表明Wnt5a激活的是经典而非非经典Wnt信号通路,因为先前的研究表明经典/非经典Wnt信号通路的激活很大程度上取决于受体。总之,我们在此报道Wnt5a介导的经典Wnt信号通路激活可能有助于正畸力诱导的骨重塑。