Olive M, Bacon W, Hildwein M
Orthod Fr. 1989;60 Pt 2:895-904.
The osteoclast is the major cellular agent of bone resorption. Hormonal stimulation of bone resorption is indirect and depends on the osteoblastic function. Protease production is the final common pathway through which osteoblastic cells initiate osteoclastic resorption. Exposition of the mineralised matrix and contact with the osteoclasts always comes before resorption, regardless of the stimulating agent involved in the resorption process. In orthodontic conditions, production and activation of osteoclasts may be attained through different ways. Inflammation subsequent to tissue damage and bioelectric perturbations associated to alveolar bending can be considered as two major events which may lead to increase bone resorption and orthodontic tooth displacement. The precise transduction mechanism of an orthodontic force into cellular resorbing activity is still obscure.
破骨细胞是骨吸收的主要细胞介质。激素对骨吸收的刺激是间接的,且依赖于成骨细胞的功能。蛋白酶的产生是成骨细胞启动破骨细胞吸收的最终共同途径。无论参与吸收过程的刺激因子是什么,矿化基质的暴露以及与破骨细胞的接触总是先于吸收发生。在正畸情况下,破骨细胞的产生和激活可以通过不同方式实现。组织损伤后的炎症以及与牙槽弯曲相关的生物电扰动可被视为可能导致骨吸收增加和正畸牙齿移动的两个主要事件。正畸力转化为细胞吸收活性的确切转导机制仍不清楚。