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EphB4/ephrinB2 信号在正畸诱导的牙根吸收后根修复中的作用。

The role of EphB4/ephrinB2 signaling in root repair after orthodontically-induced root resorption.

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Orthodontics, West China School and Hospital of Stomatology, Sichuan University, Chengdu, China.

Oral Diagnosis and Treatment Center, Aviation General Hospital, China Medical University, Beijing, China.

出版信息

Am J Orthod Dentofacial Orthop. 2021 Mar;159(3):e217-e232. doi: 10.1016/j.ajodo.2020.07.035. Epub 2021 Jan 22.

Abstract

INTRODUCTION

This study aimed to investigate the effect of EphB4/ephrinB2 signaling on orthodontically-induced root resorption repair and the possible molecular mechanism behind it.

METHODS

Seventy-two 6-week-old male Wistar rats were randomly divided into 3 groups: blank control group, physiological regeneration group (PHY), and EphB4 inhibitor local injection group (INH). A root repair model was built on experimental rats of the PHY and INH groups. The animals in the INH groups received a daily periodontal local injection of EphB4 inhibitor NVP-BHG712, whereas the blank control group and PHY groups received only the vehicle.

RESULTS

Histologic staining and microcomputed tomography analysis showed that root regeneration was inhibited in the INH group compared with the PHY group with a greater number of osteoclasts. Immunohistochemical staining showed active EphB4/ephrinB2 signaling activities during root regeneration. The cementogenesis-related factors cementum attachment protein, alkaline phosphatase, osteopontin, and runt-related transcription factor 2, and osteoclastic-related factors RANKL and osteoprotegerin were affected by regulated EphB4/ephrinB2 signaling.

CONCLUSIONS

These findings demonstrated that the EphB4/ephrinB2 signaling might be a promising therapeutic target for novel therapeutic approaches to reduce orthodontically-induced root resorption through enhancement of cementogenesis.

摘要

简介

本研究旨在探讨 EphB4/ephrinB2 信号对正畸诱导的牙根吸收修复的影响及其可能的分子机制。

方法

将 72 只 6 周龄雄性 Wistar 大鼠随机分为 3 组:空白对照组、生理再生组(PHY)和 EphB4 抑制剂局部注射组(INH)。在 PHY 组和 INH 组的实验大鼠中建立牙根修复模型。INH 组每天接受牙周局部注射 EphB4 抑制剂 NVP-BHG712,而空白对照组和 PHY 组仅接受载体。

结果

组织学染色和微计算机断层扫描分析表明,与 PHY 组相比,INH 组的牙根再生受到抑制,破骨细胞数量更多。免疫组织化学染色显示,在牙根再生过程中 EphB4/ephrinB2 信号具有活跃的活性。牙骨质附着蛋白、碱性磷酸酶、骨桥蛋白和 runt 相关转录因子 2 等成牙骨质相关因子,以及 RANKL 和骨保护素等破骨细胞相关因子受调节的 EphB4/ephrinB2 信号的影响。

结论

这些发现表明,EphB4/ephrinB2 信号可能是一种有前途的治疗靶点,可通过增强成牙骨质作用来减少正畸诱导的牙根吸收。

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