Department of Orthodontics, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Germany.
Institute of Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Clin Oral Investig. 2021 Feb;25(2):593-601. doi: 10.1007/s00784-020-03503-1. Epub 2020 Aug 15.
The transcription factor c-Fos controls the differentiation of osteoclasts and is expressed in periodontal ligament cells after mechanical stimulation in vitro. However, it is unclear how c-Fos regulates orthodontic tooth movement (OTM) in vivo. The aim of this study was therefore to analyse OTM in transgenic mice with overexpression of c-Fos.
We employed c-Fos transgenic mice (c-Fos tg) and wild-type littermates (WT) in a model of OTM induced by Nitinol tension springs that were bonded between the left first maxillary molars and the upper incisors. The unstimulated contralateral side served as an internal control. Mice were analysed by contact radiography, micro-computed tomography, decalcified histology and histochemistry.
Our analysis of the unstimulated side revealed that alveolar bone and root morphology were similar between c-Fos tg and control mice. However, we observed more osteoclasts in the alveolar bone of c-Fos tg mice as tartrate-resistant acid phosphatase (TRAP)-positive cells were increased by 40%. After 12 days of OTM, c-Fos tg mice exhibited 62% increased tooth movement as compared with WT mice. Despite the faster tooth movement, c-Fos tg and WT mice displayed the same amount of root resorption. Importantly, we did not observe orthodontically induced tissue necrosis (i.e. hyalinization) in c-Fos tg mice, while this was a common finding in WT mice.
Overexpression of c-Fos accelerates tooth movement without causing more root resorption.
Accelerated tooth movement must not result in more root resorption as higher tissue turnover may decrease the amount of mechanically induced tissue necrosis.
转录因子 c-Fos 控制破骨细胞的分化,并在体外机械刺激后牙周膜细胞中表达。然而,c-Fos 如何调节体内正畸牙齿移动(OTM)尚不清楚。因此,本研究旨在分析过表达 c-Fos 的转基因小鼠的 OTM。
我们在由 Nitinol 张力弹簧诱导的 OTM 模型中使用 c-Fos 转基因小鼠(c-Fos tg)和野生型同窝仔(WT),左侧第一上颌磨牙和上切牙之间的弹力丝作为对照。未受刺激的对侧作为内部对照。通过接触放射摄影术、微计算机断层扫描、脱钙组织学和组织化学分析对小鼠进行分析。
我们对未受刺激侧的分析表明,牙槽骨和根形态在 c-Fos tg 和对照小鼠之间相似。然而,我们观察到 c-Fos tg 小鼠的牙槽骨中有更多的破骨细胞,因为抗酒石酸酸性磷酸酶(TRAP)阳性细胞增加了 40%。在 OTM 12 天后,c-Fos tg 小鼠的牙齿移动量比 WT 小鼠增加了 62%。尽管牙齿移动更快,但 c-Fos tg 和 WT 小鼠的根吸收量相同。重要的是,我们没有观察到 c-Fos tg 小鼠的正畸诱导组织坏死(即玻璃样变),而 WT 小鼠中这种情况很常见。
c-Fos 的过表达加速了牙齿移动,而不会导致更多的根吸收。
加速牙齿移动不应导致更多的根吸收,因为更高的组织周转率可能会减少机械诱导的组织坏死量。