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正畸力作用下大鼠磨牙牙根吸收陷窝中 RANKL/RANK 和 M-CSF/c-fms 的表达

Expressions of RANKL/RANK and M-CSF/c-fms in root resorption lacunae in rat molar by heavy orthodontic force.

机构信息

Department of Orthodontics, Nihon University School of Dentistry at Matsudo, Matsudo, Chiba, Japan.

出版信息

Eur J Orthod. 2011 Aug;33(4):335-43. doi: 10.1093/ejo/cjq068. Epub 2010 Sep 10.

Abstract

The differentiation and functions of osteoclasts are regulated by receptor activator of nuclear factor-κB (RANK)/receptor activator of nuclear factor-κB ligand (RANKL) system that stimulates osteoclasts formation. Macrophage colony-stimulating factor (M-CSF) is also essential for osteoclastogenesis. A recent immunocytochemical study reported that RANKL/RANK and M-CSF/c-fms were localized in the periodontal ligament of rat molars during experimental orthodontic tooth movement. The present study focused on the expressions of RANKL/RANK and M-CSF/c-fms in root resorption area during experimental tooth movement in rats. Forty 6-week-old male Wistar rats were subjected to an orthodontic force of 10 or 50 g with a closed coil spring (wire size: 0.005 inch, diameter: 1/12 inch) ligated to the maxillary first molar cleat by a 0.008 inch stainless steel ligature wire to induce a mesial tipping movement of the upper first molars. Experimental tooth movement was undertaken for 10 days. Each sample was sliced into 6 μm continuous sections in a horizontal direction and prepared for haematoxylin and eosin (H and E) and immunohistochemistry staining for tartrate-resistant acid phosphatase (TRAP), RANK, RANKL M-CSF, and c-fms in root resorption area. Statistical analysis was carried out using a Mann-Whitney U-test with a significance level of P<0.01. On days 7 and 10, immunoreactivity for RANKL/RANK and M-CSF/c-fms was detected in odontoclasts with an orthodontic force of 50 g, but not 10 g. Therefore, RANKL/RANK and M-CSF/c-fms systems may be involved in the process of root resorption by heavy orthodontic force.

摘要

破骨细胞的分化和功能受核因子-κB 受体激活剂(RANK)/核因子-κB 受体激活剂配体(RANKL)系统的调节,该系统刺激破骨细胞的形成。巨噬细胞集落刺激因子(M-CSF)对于破骨细胞的形成也是必不可少的。最近的一项免疫细胞化学研究报告称,在实验性正畸牙齿移动期间,RANKL/RANK 和 M-CSF/c-fms 定位于大鼠磨牙的牙周韧带中。本研究重点研究了在大鼠实验性牙齿移动过程中,RANKL/RANK 和 M-CSF/c-fms 在根吸收区域的表达。40 只 6 周龄雄性 Wistar 大鼠用闭合线圈弹簧(线径:0.005 英寸,直径:1/12 英寸)施加 10 或 50g 的正畸力,通过 0.008 英寸不锈钢结扎丝结扎在上颌第一磨牙的 cleat 上,以诱导上颌第一磨牙的近中倾斜运动。进行了 10 天的实验性牙齿移动。每个样本在水平方向上切成 6μm 连续切片,并准备用于根吸收区的苏木精和伊红(H 和 E)以及抗酒石酸酸性磷酸酶(TRAP)、RANK、RANKL M-CSF 和 c-fms 的免疫组织化学染色。使用 Mann-Whitney U 检验进行统计分析,显著性水平为 P<0.01。在第 7 天和第 10 天,在施加 50g 正畸力的情况下,破骨细胞中检测到 RANKL/RANK 和 M-CSF/c-fms 的免疫反应性,但施加 10g 正畸力时则没有。因此,RANKL/RANK 和 M-CSF/c-fms 系统可能参与了重正畸力导致的牙根吸收过程。

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