Jeon Hyeran Helen, Teixeira Hellen, Tsai Andrew
Department of Orthodontics, School of Dental Medicine, University of Pennsylvania, 240 South 40th Street, Philadelphia, PA 19104-6030, USA.
J Clin Med. 2021 Apr 16;10(8):1733. doi: 10.3390/jcm10081733.
Alveolar bone remodeling in orthodontic tooth movement (OTM) is a highly regulated process that coordinates bone resorption by osteoclasts and new bone formation by osteoblasts. Mechanisms involved in OTM include mechano-sensing, sterile inflammation-mediated osteoclastogenesis on the compression side and tensile force-induced osteogenesis on the tension side. Several intracellular signaling pathways and mechanosensors including the cilia and ion channels transduce mechanical force into biochemical signals that stimulate formation of osteoclasts or osteoblasts. To date, many studies were performed in vitro or using human gingival crevicular fluid samples. Thus, the use of transgenic animals is very helpful in examining a cause and effect relationship. Key cell types that participate in mediating the response to OTM include periodontal ligament fibroblasts, mesenchymal stem cells, osteoblasts, osteocytes, and osteoclasts. Intercellular signals that stimulate cellular processes needed for orthodontic tooth movement include receptor activator of nuclear factor-κB ligand (RANKL), tumor necrosis factor-α (TNF-α), dickkopf Wnt signaling pathway inhibitor 1 (DKK1), sclerostin, beta (), and bone morphogenetic proteins (BMPs). In this review, we critically summarize the current OTM studies using transgenic animal models in order to provide mechanistic insight into the cellular events and the molecular regulation of OTM.
正畸牙齿移动(OTM)过程中的牙槽骨重塑是一个高度受调控的过程,它协调破骨细胞介导的骨吸收和成骨细胞介导的新骨形成。OTM涉及的机制包括机械感知、压缩侧无菌性炎症介导的破骨细胞生成以及张力侧拉力诱导的成骨作用。包括纤毛和离子通道在内的几种细胞内信号通路和机械传感器将机械力转化为生化信号,刺激破骨细胞或成骨细胞的形成。迄今为止,许多研究是在体外或使用人类龈沟液样本进行的。因此,转基因动物的使用对于研究因果关系非常有帮助。参与介导对OTM反应的关键细胞类型包括牙周膜成纤维细胞、间充质干细胞、成骨细胞、骨细胞和破骨细胞。刺激正畸牙齿移动所需细胞过程的细胞间信号包括核因子κB受体激活剂配体(RANKL)、肿瘤坏死因子-α(TNF-α)、Dickkopf Wnt信号通路抑制剂1(DKK1)、硬化蛋白、β()和骨形态发生蛋白(BMP)。在这篇综述中,我们批判性地总结了目前使用转基因动物模型进行的OTM研究,以便深入了解OTM的细胞事件和分子调控机制。