Mechanosensor YAP mediates bone remodeling via NF-κB p65 induced osteoclastogenesis during orthodontic tooth movement.

IF 4.8 2区 医学 Q1 Dentistry Progress in Orthodontics Pub Date : 2025-01-02 DOI:10.1186/s40510-024-00548-w
Jie Deng, Yu-Ning Zhang, Ru-Shui Bai, Ting-Ting Yu, Yi Zhao, Hao Liu, Yun-Fan Zhang, Tian-Min Xu, Bing Han
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Abstract

Background: Yes-associated protein (YAP) is a crucial mechanosensor involved in mechanotransduction, but its role in regulating mechanical force-induced bone remodeling during orthodontic tooth movement (OTM) is unclear. This study aims to elucidate the relationship between mechanotransduction and mechanical force-induced alveolar bone remodeling during OTM.

Results: Our study confirms an asynchronous (temporal and spatial sequence) remodeling pattern of the alveolar bone under mechanical force during OTM. Both compression and tension activate osteoclasts recruiting to the alveolar bone, whereas no significant presence of osteoblasts in the alveolar bone at the early stages of bone remodeling. Specifically, applying different force magnitudes (10, 25, 50, 100 g) to rats' 1st molars affected OTM distance. Force-induced alveolar bone remodeling was characterized by osteoclastogenesis and YAP activation at compressive/tensile sites on day 1 of OTM. Notably, 25 g force triggered peak YAP expression and osteoclastic activity early on. Time-course analysis revealed two YAP activity peaks on day1 and 14, contrasting with one peak of type I collagen expression on day14. In addition, RNA-sequencing highlighted increased nuclear factor kappa B (NF-κB) signaling, mineral absorption, and osteoclast differentiation at day-1 and 3. Moreover, gene expression analysis showed similar trends for NF-κB p65, YAP1, and TEA domain 1 (TEAD1) during this time. Furthermore, experiments on osteoclast cultures indicated YAP activation via large tumor suppressor (LATS) and TEAD under mechanical stimuli (compression/tension), promoting osteoclastogenesis by regulating NF-κB p65 and receptor activator of NF-κB (RANK). Inhibiting YAP with verteporfin delayed OTM by impairing force-induced osteoclastic activities in vivo and ex-vivo.

Conclusions: We propose that YAP mediates alveolar bone remodeling through NF-κB p65-induced osteoclastogenesis in an asynchronous remodeling pattern during OTM. Both compression and tension activate osteoclasts recruiting to the alveolar bone at early stages of bone remodeling, offering evidence for orthodontists as a reference.

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在正畸牙齿移动过程中,机械传感器YAP通过NF-κB p65诱导的破骨细胞生成介导骨重塑。
背景:Yes-associated protein (YAP)是参与机械转导的重要机械传感器,但其在正畸牙齿运动(OTM)过程中调节机械力诱导的骨重塑中的作用尚不清楚。本研究旨在阐明骨外伤性骨移植过程中机械力传导与机械力诱导的牙槽骨重塑之间的关系。结果:我们的研究证实了机械力作用下牙槽骨的非同步(时间和空间顺序)重塑模式。挤压和张力均能激活破骨细胞向牙槽骨募集,而在骨重塑的早期阶段,牙槽骨中没有明显的成骨细胞存在。具体而言,施加不同大小的力(10、25、50、100 g)对大鼠第一磨牙的OTM距离有影响。力诱导的牙槽骨重塑的特征是在OTM第1天破骨细胞生成和YAP在压缩/拉伸部位的激活。值得注意的是,25g力在早期触发了YAP表达和破骨细胞活性的峰值。时间过程分析显示,YAP活性在第1天和第14天出现两个高峰,而I型胶原表达在第14天出现一个高峰。此外,rna测序显示,在第1天和第3天,核因子κB (NF-κB)信号传导、矿物质吸收和破骨细胞分化增加。此外,在这段时间内,基因表达分析显示NF-κB p65、YAP1和TEA结构域1 (TEAD1)的表达趋势相似。此外,破骨细胞培养实验表明,在机械刺激(压迫/张力)下,YAP通过大肿瘤抑制因子(large tumor suppressor, LATS)和TEAD激活,通过调节NF-κB p65和NF-κB受体激活因子(receptor activator of NF-κB, RANK)促进破骨细胞生成。通过在体内和离体损伤力诱导的破骨细胞活性来抑制YAP延迟OTM。结论:我们认为YAP通过NF-κB p65诱导的破骨细胞在OTM过程中以非同步重塑模式介导牙槽骨重塑。在骨重塑的早期阶段,挤压和张力均可激活破骨细胞向牙槽骨募集,为正畸医生提供参考依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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索莱宝
goat anti-rabbit IgG-HRP
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goat anti-mouse IgG-HRP
索莱宝
HRP-conjugated goat anti-mouse IgG
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DAPI
来源期刊
Progress in Orthodontics
Progress in Orthodontics Dentistry-Orthodontics
CiteScore
7.30
自引率
4.20%
发文量
45
审稿时长
13 weeks
期刊介绍: Progress in Orthodontics is a fully open access, international journal owned by the Italian Society of Orthodontics and published under the brand SpringerOpen. The Society is currently covering all publication costs so there are no article processing charges for authors. It is a premier journal of international scope that fosters orthodontic research, including both basic research and development of innovative clinical techniques, with an emphasis on the following areas: • Mechanisms to improve orthodontics • Clinical studies and control animal studies • Orthodontics and genetics, genomics • Temporomandibular joint (TMJ) control clinical trials • Efficacy of orthodontic appliances and animal models • Systematic reviews and meta analyses • Mechanisms to speed orthodontic treatment Progress in Orthodontics will consider for publication only meritorious and original contributions. These may be: • Original articles reporting the findings of clinical trials, clinically relevant basic scientific investigations, or novel therapeutic or diagnostic systems • Review articles on current topics • Articles on novel techniques and clinical tools • Articles of contemporary interest
期刊最新文献
Patient experiences and discomfort associated with mid-palatal temporary skeletal anchorage devices. Three-dimensional quantitative temporomandibular joint changes in skeletal class I malocclusion treated with extraction and non-extraction protocols: a comparative study of fixed orthodontic appliances and clear aligners. Tooth wear and tertiary crowding: a 13-year cohort study in Amazon Indigenous populations. Correction to: Effect of anti-sclerostin antibody on orthodontic tooth movement in ovariectomized rats. Mechanosensor YAP mediates bone remodeling via NF-κB p65 induced osteoclastogenesis during orthodontic tooth movement.
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