Department of Orthodontics, University Hospital Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, Germany.
Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, Germany; Institute for Medical Microbiology, Immunology and Hygiene, University Cologne, Goldenfelsstraße 19-21, 50935 Cologne, Germany.
Ann Anat. 2022 Oct;244:151979. doi: 10.1016/j.aanat.2022.151979. Epub 2022 Jul 3.
The aim of the study was to investigate the impact of dietary salt and the osmoprotective transcription factor nuclear factor of activated T cells 5 (NFAT5) in myeloid cells on bone remodelling cells as osteocytes, osteoblasts and osteoclasts and on force-induced dental root resorptions in a mouse model.
Control mice and mice lacking myeloid NFAT5 (nuclear factor of activated T cells 5) were either kept on low, normal or high salt diets. After one week on the specified diet an elastic band was inserted between the first and second molar to induce orthodontic tooth movement. One week later the mice were euthanised and jaws were fixed for histological analysis. Osteocyte, osteoblast and osteoclast numbers as well as extent of root resorptions were assessed histologically.
Osteocyte number was diminished with high salt diet in wildtype mice. Osteoblast numbers increased with low salt diet in control mice and reduced with high salt diet in mice without NFAT5 in myeloid cells. High salt diet tended to increase osteoclast number in control mice. In mice without myeloid NFAT5, numbers of osteoclasts were reduced under high salt diet. Frequency of force-induced root resorptions tended to be dependent on dietary salt content in control mice.
During orthodontic tooth movement dietary salt impacts on the frequency of root resorptions and the number of osteoclasts and osteoblasts in alveolar bone of mice. This can affect bone remodelling during orthodontic treatment. Myeloid NFAT5 impacts on this salt-dependent reaction.
本研究旨在探讨膳食盐和髓系细胞中核因子活化 T 细胞 5(NFAT5)的渗透保护转录因子对成骨细胞、成骨细胞和破骨细胞等骨重塑细胞以及在小鼠模型中力诱导的牙根吸收的影响。
对照组和缺乏髓系 NFAT5(核因子活化 T 细胞 5)的小鼠分别给予低、正常或高盐饮食。在特定饮食 1 周后,将弹性带插入第一和第二磨牙之间以诱导正畸牙齿移动。1 周后,处死小鼠并固定颌骨进行组织学分析。通过组织学评估骨细胞、成骨细胞和破骨细胞的数量以及牙根吸收的程度。
野生型小鼠高盐饮食导致骨细胞数量减少。对照组小鼠低盐饮食导致成骨细胞数量增加,而髓系细胞中缺乏 NFAT5 的小鼠高盐饮食导致成骨细胞数量减少。高盐饮食可能会增加对照组小鼠破骨细胞的数量。在缺乏髓系 NFAT5 的小鼠中,高盐饮食下破骨细胞数量减少。力诱导的牙根吸收频率似乎依赖于对照组小鼠的饮食盐含量。
在正畸牙齿移动过程中,饮食盐会影响小鼠牙槽骨中牙根吸收的频率以及破骨细胞和成骨细胞的数量。这可能会影响正畸治疗中的骨重塑。髓系 NFAT5 会影响这种盐依赖性反应。