Department of Bone Metabolism, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, China; Center of Osteoporosis and Bone Mineral Research, Shandong University, China.
Department of Oral and Maxillofacial Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 324 Jingwu Road, 250021 Jinan, China.
Cell Signal. 2023 Aug;108:110724. doi: 10.1016/j.cellsig.2023.110724. Epub 2023 May 19.
Orthodontic treatment in older adults is more difficult than in younger adults, partially due to delayed osteogenesis caused by senescence of human periodontal ligament stem cells (hPDLSCs). The production of brain-derived neurotrophic factor (BDNF) which regulates the differentiation and survival of stem cells decreases with age. We aimed to investigate the relationship between BDNF and hPDLSC senescence and its effects on orthodontic tooth movement (OTM). We constructed mouse OTM models using orthodontic nickel‑titanium springs and compared the responses of wild-type (WT) and BDNF mice with or without addition of exogenous BDNF. In vitro, hPDLSCs subjected to the mechanical stretch were used to simulate the cell stretch environment during OTM. We extracted periodontal ligament cells from WT and BDNF mice to evaluate their senescence-related indicators. The application of orthodontic force increased BDNF expression in the periodontium of WT mice, while the mechanical stretch increased BDNF expression in hPDLSCs. Osteogenesis-related indicators, including RUNX2 and ALP decreased and cellular senescence-related indicators such as p16, p53 and β-galactosidase increased in BDNF mice periodontium. Furthermore, periodontal ligament cells extracted from BDNF mice exhibited more senescent compared with cells from WT mice. Application of exogenous BDNF decreased the expression of senescence-related indicators in hPDLSCs by inhibiting Notch3, thereby promoting osteogenic differentiation. Periodontal injection of BDNF decreased the expression of senescence-related indicators in periodontium of aged WT mice. In conclusion, our study showed that BDNF promotes osteogenesis during OTM by alleviating hPDLSCs senescence, paving a new path for future research and clinical applications.
正畸治疗在老年人中比在年轻人中更困难,部分原因是人类牙周韧带干细胞(hPDLSCs)衰老导致成骨延迟。调节干细胞分化和存活的脑源性神经营养因子(BDNF)的产生随着年龄的增长而减少。我们旨在研究 BDNF 与 hPDLSC 衰老之间的关系及其对正畸牙齿移动(OTM)的影响。我们使用正畸镍钛弹簧构建了小鼠 OTM 模型,并比较了野生型(WT)和 BDNF 小鼠在有无外源性 BDNF 加入时的反应。在体外,我们使用机械拉伸来模拟 OTM 期间细胞拉伸环境,从而对 hPDLSCs 进行处理。我们从 WT 和 BDNF 小鼠中提取牙周韧带细胞,以评估其与衰老相关的指标。正畸力的应用增加了 WT 小鼠牙周组织中的 BDNF 表达,而机械拉伸增加了 hPDLSCs 中的 BDNF 表达。骨形成相关指标,包括 RUNX2 和 ALP 降低,而 BDNF 小鼠牙周组织中的细胞衰老相关指标,如 p16、p53 和β-半乳糖苷酶增加。此外,与 WT 小鼠的细胞相比,BDNF 小鼠的牙周韧带细胞表现出更多的衰老。应用外源性 BDNF 通过抑制 Notch3 降低了 hPDLSCs 中衰老相关指标的表达,从而促进成骨分化。BDNF 牙周注射降低了老年 WT 小鼠牙周组织中衰老相关指标的表达。总之,我们的研究表明,BDNF 通过减轻 hPDLSCs 衰老来促进 OTM 中的骨形成,为未来的研究和临床应用开辟了新的途径。