Väänänen H K
Department of Anatomy, University of Oulu, Finland.
Ann Med. 1993 Aug;25(4):353-9. doi: 10.3109/07853899309147297.
Bone remodelling is a cellular mechanism behind the bone turnover. It renews the old bone piece by piece and thus ensures the correction of possible microdamage and enables the regulation of mineral homeostasis. The basic mechanism of bone remodelling is similar in all types of bone and includes the resorption of old bone and the formation of equal amount of new bone at the same place. Histomorphometric studies have revealed the cellular details of remodelling and have shown that it is composed by the temporally and spatially regulated action of different bone cells and their precursors. Recent in vitro studies with osteoclasts and osteoblasts have increased our knowledge of the molecular mechanisms of bone remodelling. Molecular characterization of bone matrix proteins have suggested new functions to many of them and thereby increased our possibilities of understanding the local regulation mechanisms of remodelling. Bone matrix has been shown to contain several biologically active compounds which have effects on bone forming and resorbing cells and their precursors. Details of the functional mechanism of osteoclasts are also in the process of being discovered. However, several questions concerning bone remodelling still remain open: the molecular explanation for selection of the remodelling site; the coupling of bone resorption to formation, and the interactions between different cell types during the remodelling cycle.
骨重塑是骨转换背后的细胞机制。它逐块更新旧骨,从而确保纠正可能的微损伤,并实现矿物质稳态的调节。骨重塑的基本机制在所有类型的骨中都是相似的,包括旧骨的吸收以及在同一位置形成等量的新骨。组织形态计量学研究揭示了重塑的细胞细节,并表明它是由不同骨细胞及其前体在时间和空间上的调节作用所组成。最近对破骨细胞和成骨细胞的体外研究增加了我们对骨重塑分子机制的了解。骨基质蛋白的分子特征揭示了其中许多蛋白的新功能,从而增加了我们理解重塑局部调节机制的可能性。已表明骨基质含有几种对骨形成和吸收细胞及其前体有影响的生物活性化合物。破骨细胞功能机制的细节也正在被发现。然而,关于骨重塑的几个问题仍然悬而未决:重塑部位选择的分子解释;骨吸收与形成的耦合,以及重塑周期中不同细胞类型之间的相互作用。