Wise G E, Lumpkin S J, Huang H, Zhang Q
Department of Veterinary Anatomy and Cell Biology, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803-8408, USA.
J Dent Res. 2000 Dec;79(12):1937-42. doi: 10.1177/00220345000790120301.
A critical cellular event in tooth eruption is the formation of osteoclasts that are needed for bone resorption to form an eruption pathway. To analyze molecular regulation of osteoclast formation and activation, we examined the expression of osteoprotegerin (OPG), an inhibitor of osteoclast formation. In vivo, the gene expression of OPG is reduced in the dental follicle of the first mandibular molar of the rat at day 3 post-natally and in the mouse at day 5. This correlates with the days of maximal mononuclear cell influx and osteoclast numbers in the rat and mouse. Thus, inhibition of OPG gene expression on these days might allow osteoclasts to be formed and/or activated. In vitro studies demonstrated that both colony-stimulating factor-1 and parathyroid hormone-related protein reduced OPG gene expression in follicle cells, suggesting that these are candidate molecules for the in vivo inhibition of OPG expression. Osteoclast differentiation factor (ODF) immunolocalizes to the alveolar bone stromal cells adjacent to the follicle, whereby it might act to stimulate fusion of the mononuclear cells in the follicle.
牙齿萌出过程中的一个关键细胞事件是破骨细胞的形成,而骨吸收形成萌出通道需要破骨细胞。为了分析破骨细胞形成和激活的分子调控机制,我们检测了骨保护素(OPG)的表达,它是一种破骨细胞形成的抑制剂。在体内,出生后第3天的大鼠以及出生后第5天的小鼠下颌第一磨牙牙囊内,OPG的基因表达降低。这与大鼠和小鼠中单核细胞大量涌入和破骨细胞数量最多的时间相吻合。因此,在这些时间抑制OPG基因表达可能会使破骨细胞得以形成和/或激活。体外研究表明,集落刺激因子-1和甲状旁腺激素相关蛋白均可降低牙囊细胞中OPG的基因表达,这表明它们可能是体内抑制OPG表达的候选分子。破骨细胞分化因子(ODF)免疫定位在与牙囊相邻的牙槽骨基质细胞上,可能起到刺激牙囊中单核细胞融合的作用。