Collin-Osdoby P
Department of Biology, Washington University, St. Louis, Missouri 63130.
J Cell Biochem. 1994 Jul;55(3):304-9. doi: 10.1002/jcb.240550306.
Bone development and remodeling depend on complex interactions between bone-forming osteoblasts, bone-degrading osteoclasts, and other cells present within the bone microenvironment. Balanced control of bone formative and degradative processes is normally carefully maintained in the adult skeleton but becomes uncoupled in the course of aging or in various pathological disease states. Systemic regulators of bone metabolism and local mediators, including matrix molecules, cytokines, prostaglandins, leukotrienes, and other autocrine or paracrine factors, regulate the recruitment, differentiation, and function of cells participating in bone formation and turnover. Although some of these interactions are now understood, many yet remain to be elucidated. Recent studies have begun exploring in detail how vascular endothelial cells and their products function in bone physiology. The findings are revealing that bone vascular endothelial cells may be members of a complex communication network in bone which operates between endothelial cells, osteoblasts, osteoclasts, macrophages, stromal cells, and perhaps other cell types found in bone as well. Therefore, multiple systemic and locally produced signals may be received, transduced, and integrated by individual cells and then propagated by the release from these cells of further signals targeted to other members of the bone cell network. In this manner, bone cell activities may be continuously coordinated to afford concerted actions and rapid responses to physiological changes. The bone microvasculature may play a pivotal role in these processes, both in linking circulatory and local signals with cells of the bone microenvironment and in actively contributing itself to the regulation of bone cell physiology.(ABSTRACT TRUNCATED AT 250 WORDS)
骨发育和重塑取决于成骨细胞、破骨细胞以及骨微环境中其他细胞之间复杂的相互作用。在成年骨骼中,通常会仔细维持骨形成和降解过程的平衡控制,但在衰老过程或各种病理疾病状态下会失衡。骨代谢的全身调节因子和局部介质,包括基质分子、细胞因子、前列腺素、白三烯和其他自分泌或旁分泌因子,调节参与骨形成和更新的细胞的募集、分化和功能。虽然现在已经了解了其中一些相互作用,但仍有许多有待阐明。最近的研究开始详细探索血管内皮细胞及其产物在骨生理学中的作用。研究结果表明,骨血管内皮细胞可能是骨中一个复杂通讯网络的成员,该网络在内皮细胞、成骨细胞、破骨细胞、巨噬细胞、基质细胞以及骨中可能存在的其他细胞类型之间运作。因此,单个细胞可能接收、转导和整合多种全身和局部产生的信号,然后通过这些细胞释放针对骨细胞网络其他成员的进一步信号来传播。通过这种方式,骨细胞活动可能会持续协调,以实现协同作用并对生理变化做出快速反应。骨微血管系统可能在这些过程中起关键作用,既将循环和局部信号与骨微环境中的细胞联系起来,又积极参与骨细胞生理学的调节。(摘要截选至250词)