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基质细胞衍生因子-1 在外源性正畸牙移动中的作用。

SDF-1 involvement in orthodontic tooth movement after tooth extraction.

机构信息

Department of Orthodontic Science, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Yushima 1-5-45, Bunkyo-ku, Tokyo, 113-8510, Japan.

Department of Orthodontics, Faculty of Dentistry, Chulalongkorn University, Bangkok, 10330, Thailand.

出版信息

Sci Rep. 2024 Feb 29;14(1):5048. doi: 10.1038/s41598-024-55632-2.

Abstract

The stromal cell-derived factor 1 (SDF-1)/chemokine receptor type 4 (CXCR4) axis plays a key role in alveolar bone metabolism during orthodontic tooth movement (OTM). Herein, the effects of the SDF-1/CXCR4 axis on the regional acceleratory phenomenon (RAP) in OTM velocity and on changes in the surrounding periodontium after adjacent tooth extraction in rats were investigated. Six-week-old male Wistar/ST rats underwent left maxillary first molar (M1) extraction and mesial OTM of the left maxillary second molar (M2) with a 10-g force closed-coil spring. Phosphate-buffered saline, immunoglobulin G (IgG) isotype control antibody, or anti-SDF-1 neutralizing monoclonal antibody were injected at the M1 and M2 interproximal areas (10 μg/0.1 mL) for the first three days. Analyses were performed after 1, 3, and 7 days (n = 7). The results demonstrated a significant increase in SDF-1 expression from day 1, which was effectively blocked via anti-SDF-1 neutralizing monoclonal antibody injection. On day 3, the M2 OTM distance and the number of positively stained osteoclasts significantly reduced alongside a reduction in inflammatory markers in the experimental group. Our results demonstrated that serial local injection of the anti-SDF-1 neutralizing monoclonal antibody reduces M2 OTM, osteoclast accumulation, and localized inflammatory responses in an OTM model with tooth extraction-induced RAP.

摘要

基质细胞衍生因子 1(SDF-1)/趋化因子受体 4(CXCR4)轴在正畸牙齿移动(OTM)期间的牙槽骨代谢中起着关键作用。在此,研究了 SDF-1/CXCR4 轴对 OTM 速度的局部加速现象(RAP)以及大鼠相邻牙齿拔除后周围牙周组织变化的影响。6 周龄雄性 Wistar/ST 大鼠接受左侧上颌第一磨牙(M1)拔除和左侧上颌第二磨牙(M2)近中 OTM,使用 10-g 力的闭圈弹簧。在 M1 和 M2 近中区域(10μg/0.1mL)注射磷酸盐缓冲盐水、免疫球蛋白 G(IgG)同种型对照抗体或抗 SDF-1 中和单克隆抗体,前三天每天注射一次。在第 1、3 和 7 天(n=7)进行分析。结果表明,从第 1 天开始 SDF-1 表达显著增加,通过注射抗 SDF-1 中和单克隆抗体可有效阻断。第 3 天,实验组 M2 OTM 距离和阳性染色破骨细胞数量明显减少,炎症标志物减少。我们的结果表明,在拔牙诱导 RAP 的 OTM 模型中,连续局部注射抗 SDF-1 中和单克隆抗体可减少 M2 OTM、破骨细胞积累和局部炎症反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1077/10904391/fcebe70601cc/41598_2024_55632_Fig1_HTML.jpg

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