Department of Oral Biology, University of Illinois at Chicago, Chicago, IL, USA.
Bone. 2010 Dec;47(6):1020-9. doi: 10.1016/j.bone.2010.08.025. Epub 2010 Sep 7.
Unloading of teeth results in extensive alveolar bone remodeling, causing teeth to move in both vertical ("super-eruption") and horizontal direction ("drift"). In order to decipher the molecular mechanisms of unloading-induced bone remodeling during tooth movement, we focused on the role of osteopontin (OPN) in the un-opposed molar model, comparing wild-type (WT) and OPN-null mice. Our data indicated that OPN was not required for the continuous eruption of un-opposed teeth while OPN was necessary for the drift of teeth. OPN expression and osteoclast counts were greatly increased on alveolar bone surfaces facing the direction of the drift in WT mice, while osteoclast counts were diminished in OPN-/- mice. RANKL expression in the distal periodontal ligament of WT molars increased significantly by day 6 following unloading, while overall levels of RANKL expression were decreased in both WT and OPN-null mice. In vitro treatment of MC3T3 cells, WT BMCs and OPN-/- BMCs with recombinant OPN resulted in significantly increased RANKL expression in all three cell types. The PI3K and MEK/ERK pathway inhibitors Ly294002 and U0126 reduced RANKL expression levels in vitro. Treatment of BMCs and MC3T3 with OPN also resulted in increased ERK phosphorylation and reduced OPG levels. Together, our studies suggest that increased OPN expression during unloading-induced drifting of teeth enhances localized RANKL expression and osteoclast activity on drift-direction alveolar bone surfaces via extracellular matrix signaling pathways.
牙齿的卸载会导致广泛的牙槽骨重塑,导致牙齿在垂直(“超萌出”)和水平方向(“漂移”)上移动。为了解读牙齿运动过程中卸载诱导的骨重塑的分子机制,我们专注于骨桥蛋白(OPN)在非对抗磨牙模型中的作用,比较了野生型(WT)和 OPN 敲除(OPN-/-)小鼠。我们的数据表明,OPN 对于非对抗牙齿的持续萌出不是必需的,而 OPN 对于牙齿的漂移是必需的。在 WT 小鼠中,面向漂移方向的牙槽骨表面上的 OPN 表达和破骨细胞计数大大增加,而 OPN-/- 小鼠中的破骨细胞计数减少。WT 磨牙远侧牙周韧带中 RANKL 的表达在卸载后第 6 天显著增加,而 WT 和 OPN-/- 小鼠中的 RANKL 表达总体水平降低。用重组 OPN 体外处理 MC3T3 细胞、WT BMCs 和 OPN-/- BMCs,导致所有三种细胞类型中的 RANKL 表达显著增加。PI3K 和 MEK/ERK 通路抑制剂 Ly294002 和 U0126 降低了体外 RANKL 的表达水平。用 OPN 处理 BMCs 和 MC3T3 还导致 ERK 磷酸化增加和 OPG 水平降低。总之,我们的研究表明,在卸载诱导的牙齿漂移过程中 OPN 表达的增加通过细胞外基质信号通路增强了局部 RANKL 表达和漂移方向牙槽骨表面上的破骨细胞活性。