拉伸力通过ephrinB2-EphB4信号通路促进正畸牙齿运动中的成骨分化。

IF 3.8 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE BMC Oral Health Pub Date : 2025-01-22 DOI:10.1186/s12903-025-05491-8
Hang Yu, Xiaoxi Wei, Huan Jiang, Huichuan Qi, Yi Zhang, Min Hu
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引用次数: 0

摘要

目的:探讨张力(TF)促进成骨细胞成骨分化是否受ephrinB2-EphB4信号通路介导。方法:将TF作用于MC3T3-E1细胞,采用CCK-8和活/死染色检测细胞增殖情况。采用ALP染色、ARS染色、qPCR和western blot检测成骨分化相关因子水平。NVP-BHG712阻断EphB4受体。采用ephrinB2-Fc和NVP-BHG712治疗大鼠,建立大鼠正畸牙齿运动模型。Micro-CT及H&E染色检测牙槽骨。通过检测MAPK通路的变化,探讨其是否在ephrinB2-EphB4信号通路的下游,介导TF促进成骨分化。结果:我们探索了TF对MC3T3-E1细胞的影响,发现TF明显促进成骨分化,但当EphB4受体被阻断时,这种促进作用被抑制。在体内,我们发现TF通过ephrinB2-EphB4信号通路促进牙槽骨形成。对信号通路的进一步研究发现,TF显著增加了MAPK通路的水平,而当EphB4受体被阻断时,只有p-ERK1/2的促进水平下降。结论:TF通过ephrinB2-EphB4信号通路促进成骨分化,ERK1/2通路是ephrinB2-EphB4信号通路的下游,部分介导TF诱导的促进成骨分化。
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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Tensile force promotes osteogenic differentiation via ephrinB2-EphB4 signaling pathway in orthodontic tooth movement.

Objective: To investigating whether osteogenic differentiation of osteoblasts promoted by tension force (TF) is mediated by ephrinB2-EphB4 signaling.

Methods: TF was applied to MC3T3-E1 cells, then CCK-8 and live/dead staining were used to detect cell proliferation. Levels of osteogenic differentiation-related factors were detected by ALP staining, ARS staining, qPCR and western blot. NVP-BHG712 was used to block EphB4 receptor. Establishing a rat orthodontic tooth movement (OTM) model, ephrinB2-Fc and NVP-BHG712 were used to treat rats. Micro-CT and H&E staining were used to detect alveolar bone. Changes of MAPK pathways were detected to investigate whether they were downstream of ephrinB2-EphB4 signaling in mediating TF promote osteogenic differentiation.

Result: We explored the effect of TF on MC3T3-E1 cells, and found that TF significantly promoted osteogenic differentiation, but when EphB4 receptor was blocked, the promotion was inhibited. In vivo, we found that TF improved alveolar bone formation through ephrinB2-EphB4 signaling. Further investigation into the signaling pathways revealed that TF significantly increased levels of MAPK pathways, however, when EphB4 receptor was blocked, only the promotion of p-ERK1/2 was decreased.

Conclusion: TF promotes osteogenic differentiation through ephrinB2-EphB4 signaling and ERK1/2 pathway is a downstream of ephrinB2-EphB4 signaling partially mediate mediates TF-induced promotion of osteogenic differentiation.

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来源期刊
BMC Oral Health
BMC Oral Health DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.90
自引率
6.90%
发文量
481
审稿时长
6-12 weeks
期刊介绍: BMC Oral Health is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the mouth, teeth and gums, as well as related molecular genetics, pathophysiology, and epidemiology.
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