Department of Oral Biology, School of Dentistry, University of Missouri, Kansas City, Missouri, USA.
Ann N Y Acad Sci. 2010 Mar;1192:437-43. doi: 10.1111/j.1749-6632.2009.05246.x.
Osteocytes are derived from osteoblasts and make up over 90% of the cells in bone. However, the mechanisms that control the differentiation of osteoblasts into osteocytes embedded in bone matrix are not well understood. With the recent developments of transgenic models for manipulating gene expression in osteocytes and of transgenic mice carrying lineage reporters for osteoblasts and osteocytes, unprecedented new insights are becoming possible. In this article we review recent advances, such as comparative gene and protein expression studies, that are delineating the changes in gene and protein expression that accompany osteocyte differentiation. We also review recent studies in which time-lapse dynamic imaging approaches have been used to visualize osteoblast and osteocyte populations within bone. These approaches reveal the key role of cell motility in bone cell function and highlight the dynamic nature of mineralized tissues. Changes in motile properties of the cell may be key in the transition from osteoblast to osteocyte, as reflected in the altered expression of many molecules involved in cytoskeletal function.
成骨细胞来源于成骨细胞,占骨细胞的 90%以上。然而,控制成骨细胞分化为嵌入骨基质中的成骨细胞的机制尚不清楚。随着近年来在成骨细胞中操纵基因表达的转基因模型和携带成骨细胞和成骨细胞谱系报告基因的转基因小鼠的发展,以前所未有的新视角成为可能。在本文中,我们回顾了最近的进展,如比较基因和蛋白质表达研究,这些研究描绘了伴随成骨细胞分化的基因和蛋白质表达的变化。我们还回顾了最近的研究,其中使用延时动态成像方法来可视化骨内的成骨细胞和破骨细胞群体。这些方法揭示了细胞迁移在骨细胞功能中的关键作用,并强调了矿化组织的动态性质。细胞迁移特性的变化可能是成骨细胞向成骨细胞转化的关键,这反映在许多参与细胞骨架功能的分子的表达改变上。