Department of Orthodontics, Affliated Hospital of Stomatology, Anhui Medical University Hefei, 69 Meishan Road, Hefei, Anhui, China; School of Dentistry, College of Medicine and Health Sciences, University of Rwanda, Rwanda.
Department of Orthodontics, Affliated Hospital of Stomatology, Anhui Medical University Hefei, 69 Meishan Road, Hefei, Anhui, China.
Ann Anat. 2024 Aug;255:152286. doi: 10.1016/j.aanat.2024.152286. Epub 2024 May 27.
The molecular mechanisms behind orthodontic tooth movements (OTM) were investigated by clarifying the role of chemical messengers released by cells.
Using the Cochrane library, Google scholar, and PubMed databases, a literature search was conducted, and studies published from 1984 to 2024 were considered.
Both bone growth and remodeling may occur when a tooth is subjected to mechanical stress. These chemicals have a significant effect on the stimulation and regulation of osteoblasts, osteoclasts, and osteocytes during alveolar bone remodeling. This regulation can take place in pathological conditions, such as periodontal diseases, or during OTM alone. This comprehensive review outlines key molecular mechanisms underlying OTM and explores various clinical assumptions associated with specific molecules and their functional domains during this process. Furthermore, clinical applications of certain molecules such as relaxin, prostaglandin E (PGE), and interleukin-1β (IL-1β) in accelerating OTM have been reported. Our findings underscore the existing gap between OTM clinical applications and basic research investigations.
A comprehensive understanding of orthodontic treatment is enriched by insights into biological systems. We reported the activation of osteoblasts, osteoclast precursor cells, osteoclasts, and osteocytes in response to mechanical stress, leading to targeted cellular and molecular interventions and facilitating rapid and regulated alveolar bone remodeling during tooth movement. Despite the shortcomings of clinical studies in accelerating OTM, this review highlights the crucial role of biological agents in this process and advocates for prioritizing high-quality human studies in future research to gain further insights from clinical trials.
通过阐明细胞释放的化学信使在正畸牙齿移动(OTM)中的作用,研究其背后的分子机制。
使用 Cochrane 图书馆、Google Scholar 和 PubMed 数据库进行文献检索,纳入 1984 年至 2024 年发表的研究。
牙齿受到机械应力时,可能会发生骨生长和重塑。这些化学物质对成骨细胞、破骨细胞和骨细胞在牙槽骨重塑过程中的刺激和调节有显著影响。这种调节可以在牙周病等病理条件下或单独的 OTM 中发生。本综述概述了 OTM 的关键分子机制,并探讨了在这个过程中与特定分子及其功能域相关的各种临床假设。此外,已经有报道称某些分子,如松弛素、前列腺素 E(PGE)和白细胞介素-1β(IL-1β),在加速 OTM 方面具有临床应用。我们的研究结果强调了 OTM 临床应用和基础研究之间存在的差距。
通过深入了解生物系统,可以丰富对正畸治疗的理解。我们报告了成骨细胞、破骨细胞前体细胞、破骨细胞和骨细胞对机械应力的激活,导致针对细胞和分子的干预,并促进牙齿移动过程中快速和受调控的牙槽骨重塑。尽管在加速 OTM 的临床研究中存在缺陷,但本综述强调了生物制剂在这一过程中的关键作用,并主张在未来的研究中优先进行高质量的人类研究,以从临床试验中获得更深入的见解。