Choi In Ho, Chung Chin Youb, Cho Tae-Joon, Yoo Won Joon
Department of Orthopedic Surgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
J Korean Med Sci. 2002 Aug;17(4):435-47. doi: 10.3346/jkms.2002.17.4.435.
Distraction osteogenesis is currently a standard method of bone lengthening. It is a viable method for the treatment of short extremities as well as extensive bone defects, because large amounts of bone can be regenerated in the distraction gap. Mechanical stimulation by distraction induces biological responses of skeletal regeneration that is accomplished by a cascade of biologic processes that may include differentiation of pluripotential tissue, angiogenesis, mineralization, and remodeling. There are complex interactions between bone-forming osteoblasts and other cells present within the bone microenvironment, particularly vascular endothelial cells that may be pivotal members of a complex interactive communication network in bone. Regenerate bone forms by three modes of ossification, which include intramembranous, enchondral, and transchondroid ossifications, although intramembraneous bone formation is the predominant mechanism of ossification. In this review we discussed the coupling between angiogenesis and mineralization, the biological and mechanical factors affecting them, the cellular and molecular events occurring during distraction osteogenesis, and the emerging modalities to accelerate regenerate bone healing and remodeling.
牵张成骨目前是一种标准的骨延长方法。它是治疗四肢短小以及广泛骨缺损的一种可行方法,因为在牵张间隙中可以再生大量的骨。牵张引起的机械刺激诱导骨骼再生的生物学反应,这是通过一系列生物学过程完成的,这些过程可能包括多能组织的分化、血管生成、矿化和重塑。成骨的成骨细胞与骨微环境中存在的其他细胞之间存在复杂的相互作用,特别是血管内皮细胞,它们可能是骨中复杂交互通讯网络的关键成员。再生骨通过三种骨化模式形成,包括膜内骨化、软骨内骨化和经软骨骨化,尽管膜内骨形成是主要的骨化机制。在这篇综述中,我们讨论了血管生成与矿化之间的耦合、影响它们的生物学和力学因素、牵张成骨过程中发生的细胞和分子事件,以及加速再生骨愈合和重塑的新兴模式。