Alves José B, Ferreira Cynthia L, Martins Aline F, Silva Gerluza A B, Alves Guilherme D, Paulino Tony P, Ciancaglini Pietro, Thedei Geraldo, Napimoga Marcelo H
Laboratory of Molecular Biology, University of Uberaba, Uberaba, MG, Brazil.
Life Sci. 2009 Nov 4;85(19-20):693-9. doi: 10.1016/j.lfs.2009.09.010. Epub 2009 Sep 29.
It has long been demonstrated that epidermal growth factor (EGF) has catabolic effects on bone. Thus, we examined the role of EGF in regulating mechanically induced bone modeling in a rat model of orthodontic tooth movement.
The maxillary first molars of rats were moved mesially using an orthodontic appliance attached to the maxillary incisor teeth. Rats were randomly divided into 4 groups: (G1) administration of PBS (phosphate buffer saline) solution (n=24); (G2) administration of empty liposomes (n=24); (G3) administration 20ng of EGF solution (n=24); and (G4) 20ng of EGF-liposomes solution (n=24). Each solution was injected in the mucosa of the left first molar adjacent to the appliance. At days 5, 10, 14 and 21 after drug administration, 6 animals of each group were sacrificed. Histomorphometric analysis was used to quantify osteoclasts (Tartrate-resistant acid phosphatase (TRAP)+cells) and tooth movement. Using immunohistochemistry assay we evaluated the RANKL (receptor activator of nuclear factor kappaB ligand) and epidermal growth factor receptor (EGFR) expression.
The EGF-liposome administration showed an increased tooth movement and osteoclast numbers compared to controls (p<0.05). This was correlated with intense RANKL expression. Both osteoblasts and osteoclasts expressed EGFR.
Local delivery of EGF-liposome stimulates osteoclastogenesis and tooth movement.
长期以来已有研究表明,表皮生长因子(EGF)对骨骼具有分解代谢作用。因此,我们在正畸牙齿移动的大鼠模型中研究了EGF在调节机械诱导的骨塑形中的作用。
使用连接到上颌切牙的正畸矫治器将大鼠的上颌第一磨牙向近中移动。大鼠被随机分为4组:(G1)给予磷酸盐缓冲盐水(PBS)溶液(n = 24);(G2)给予空脂质体(n = 24);(G3)给予20 ng EGF溶液(n = 24);以及(G4)给予20 ng EGF-脂质体溶液(n = 24)。每种溶液均注射到矫治器附近左侧第一磨牙的黏膜中。给药后第5、10、14和21天,每组处死6只动物。采用组织形态计量学分析来量化破骨细胞(抗酒石酸酸性磷酸酶(TRAP)阳性细胞)和牙齿移动情况。使用免疫组织化学分析评估核因子κB受体活化因子配体(RANKL)和表皮生长因子受体(EGFR)的表达。
与对照组相比,给予EGF-脂质体后牙齿移动增加且破骨细胞数量增多(p<0.05)。这与强烈的RANKL表达相关。成骨细胞和破骨细胞均表达EGFR。
局部递送EGF-脂质体可刺激破骨细胞生成和牙齿移动。