Nakano Yoko, Yamaguchi Masaru, Shimizu Mami, Kikuta Jun, Yoshino Tomokazu, Tanimoto Yasuhiro, Kasai Kazutaka
Assistant professor, Department of Orthodontics, School of Dentistry, Nihon University, Matsudo, Chiba, Japan.
Associate professor, Department of Orthodontics, School of Dentistry, Nihon University, Matsudo, Chiba, Japan.
Am J Orthod Dentofacial Orthop. 2015 Aug;148(2):302-9. doi: 10.1016/j.ajodo.2015.03.023.
The objectives of this study were (1) to investigate the expressions of interleukin (IL)-17, RANKL (the receptor activator of NF-kappaB ligand), and osteoprotegerin (OPG) in root resorption areas during experimental tooth movement in rats, and (2) to determine the effect of IL-17 on the expressions of RANKL and OPG mRNA from human dental pulp cells.
Twelve male 6-week-old Wistar rats were subjected to an orthodontic force of 50 g to induce a mesially tipping movement of the maxillary first molars for 7 days. The expression levels of tartrate resistant acid phosphatase (TRAP), interleukin (IL)-17, IL-17 receptor (IL-17R), receptor activator of nuclear factor-kappa B ligand (RANKL), and OPG proteins were determined in dental pulp by immunohistochemical analysis. Furthermore, the effects of IL-17 on the expressions of RANKL and OPG mRNA were investigated using human dental pulp cells in vitro.
In the experimental tooth movements in vivo, resorption lacunae with multinucleated cells were observed in the 50-g group. The immunoreactivities for IL-17, IL-17R, and RANKL were detected in dental pulp tissues subjected to the orthodontic force on day 7. Moreover, IL-17 increased the mRNA expression of RANKL from human dental pulp cells in vitro.
The results of this study suggest that IL-17 and RANKL may be involved in the process of orthodontically induced inflammatory root resorption in dental pulp cells.
本研究的目的是:(1)研究白细胞介素(IL)-17、核因子κB受体活化因子配体(RANKL)和骨保护素(OPG)在大鼠实验性牙齿移动过程中牙根吸收区域的表达;(2)确定IL-17对人牙髓细胞中RANKL和OPG mRNA表达的影响。
12只6周龄雄性Wistar大鼠接受50 g正畸力,诱导上颌第一磨牙近中倾斜移动7天。通过免疫组织化学分析确定牙髓中抗酒石酸酸性磷酸酶(TRAP)、白细胞介素(IL)-17、IL-17受体(IL-17R)、核因子κB受体活化因子配体(RANKL)和OPG蛋白的表达水平。此外,在体外使用人牙髓细胞研究IL-17对RANKL和OPG mRNA表达的影响。
在体内实验性牙齿移动中,50-g组观察到有含多核细胞的吸收陷窝。在第7天接受正畸力的牙髓组织中检测到IL-17、IL-17R和RANKL的免疫反应性。此外,IL-17在体外增加了人牙髓细胞中RANKL的mRNA表达。
本研究结果表明,IL-17和RANKL可能参与牙髓细胞正畸诱导的炎性牙根吸收过程。