Zhou Jianping, Feng Gang, Zhou Wenwen, Ren Aishu, Wu Yang, Zhang Dingming, Dai Hongwei
Department of Orthodontics, The Affiliated Hospital of Stomatology, Chongqing Medical University, NO.7 Shangqingsi Road, Yuzhong District, 400015, Chongqing, China.
J Orofac Orthop. 2011 Nov;72(6):457-68. doi: 10.1007/s00056-011-0050-3. Epub 2011 Nov 30.
The aim of this study was to investigate the expression patterns of osteoprotegerin (OPG) and the receptor activator of nuclear factor κB ligand (RANKL) in root resorption during orthodontic tooth movement.
Forty 12-week-old male SD rats were used with the right maxillary side as the experimental group and the left maxillary side as the control group. After 1 N (100g) force was loaded on the right maxillary first molar, the rats were sacrificed on days 0, 1, 4, 8, and 12. Mesial root resorption of the first molar, the number of odontoclasts and osteoclasts, and OPG and RANKL mRNA expression were determined by hematoxylin-eosin and scanning electron microscopy, tartrate-resistant acid phosphate staining, and in situ hybridization, respectively.
Serious root resorption was apparent on the pressure side of the mesial root of the right maxillary first molar on days 8 and 12. The number of odontoclasts in the cementum lacuna was elevated on days 8 and 12. OPG expression rose significantly on the tensile side, while RANKL expression increased on the pressure side. The mRNA level of RANKL was significantly elevated on days 4, 8, and 12. Moreover, the RANKL/OPG mRNA ratio was increased on the pressure side, but decreased on the tensile side.
Changes in the expression of RANKL mRNA and the RANKL/OPG mRNA ratio are accompanied by a parallel alteration in the number of odontoclasts and tooth resorption, suggesting crucial involvement of RANKL and OPG in tooth resorption.
本研究旨在探讨正畸牙移动过程中牙根吸收时骨保护素(OPG)和核因子κB受体活化因子配体(RANKL)的表达模式。
选用40只12周龄雄性SD大鼠,右侧上颌作为实验组,左侧上颌作为对照组。在右侧上颌第一磨牙施加1N(100g)力后,于第0、1、4、8和12天处死大鼠。分别通过苏木精-伊红染色和扫描电子显微镜、抗酒石酸酸性磷酸酶染色及原位杂交检测第一磨牙近中牙根吸收情况、破牙细胞和成骨细胞数量以及OPG和RANKL mRNA表达。
在第8天和第12天,右侧上颌第一磨牙近中牙根的压力侧出现明显的严重牙根吸收。在第8天和第12天,牙骨质陷窝内破牙细胞数量增加。拉伸侧OPG表达显著升高,而压力侧RANKL表达增加。在第4、8和12天,RANKL的mRNA水平显著升高。此外,压力侧RANKL/OPG mRNA比值升高,而拉伸侧降低。
RANKL mRNA表达及RANKL/OPG mRNA比值的变化与破牙细胞数量及牙齿吸收的平行改变相伴,提示RANKL和OPG在牙齿吸收中起关键作用。