Kitaura H, Yoshimatsu M, Fujimura Y, Eguchi T, Kohara H, Yamaguchi A, Yoshida N
Divisions of Orthodontic and Dentofacial Orthopedics, Department of Translational Medicine, Course of Medical and Dental Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8588, Japan.
J Dent Res. 2008 Apr;87(4):396-400. doi: 10.1177/154405910808700405.
Orthodontic force induces osteoclastogenesis in vivo. It has recently been reported that administration of an antibody against the macrophage-colony-stimulating factor (M-CSF) receptor c-Fms blocks osteoclastogenesis and bone erosion induced by tumor necrosis factor-alpha (TNF-alpha) administration. This study aimed to examine the effect of an anti-c-Fms antibody on mechanical loading-induced osteoclastogenesis and osteolysis in an orthodontic tooth movement model in mice. Using TNF receptor 1- and 2-deficient mice, we showed that orthodontic tooth movement was mediated by TNF-alpha. We injected anti-c-Fms antibody daily into a local site, for 12 days, during mechanical loading. The anti-c-Fms antibody significantly inhibited orthodontic tooth movement, markedly reduced the number of osteoclasts in vivo, and inhibited TNF-alpha-induced osteoclastogenesis in vitro. These findings suggest that M-CSF plays an important role in mechanical loading-induced osteoclastogenesis and bone resorption during orthodontic tooth movement mediated by TNF-alpha.
正畸力可在体内诱导破骨细胞生成。最近有报道称,给予抗巨噬细胞集落刺激因子(M-CSF)受体c-Fms抗体可阻断由肿瘤坏死因子-α(TNF-α)给药诱导的破骨细胞生成和骨侵蚀。本研究旨在探讨抗c-Fms抗体对小鼠正畸牙移动模型中机械负荷诱导的破骨细胞生成和骨溶解的影响。利用肿瘤坏死因子受体1和2缺陷型小鼠,我们发现正畸牙移动是由TNF-α介导的。在机械负荷期间,我们每天向局部部位注射抗c-Fms抗体,持续12天。抗c-Fms抗体显著抑制正畸牙移动,显著减少体内破骨细胞数量,并在体外抑制TNF-α诱导的破骨细胞生成。这些发现表明,M-CSF在由TNF-α介导的正畸牙移动过程中机械负荷诱导的破骨细胞生成和骨吸收中起重要作用。