Yoshikawa H
Department of Orthopaedic Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases.
Nihon Rinsho. 1998 Jun;56(6):1400-5.
Bone tissues continuously renew themselves to maintain their bone volume and mechanical strength. Sequence of the cellular events at the site of bone remodeling is as follows: (1) Activation; osteoclast progenitors are activated and differentiated. (2) Resorption; osteoclasts resorb a certain volume of bone by removing bone matrix and mineral. (3) Formation; osteoblasts differentiate and form new bone. The cellular coupling in space and time between osteoclastic resorption and osteoblastic formation is regulated not only by systemic hormones (estrogen, PTH, calcitonin, or vitamin D etc.) and local factors (TGF-beta, BMPs, IGFs, prostaglandins, interleukins, or TNF-alpha, etc.), but also by mechanical stress. We review the various regulators for bone remodeling and comment on the regulatory mechanism of bone remodeling.
骨组织不断自我更新以维持其骨量和机械强度。骨重塑部位细胞事件的顺序如下:(1) 激活;破骨细胞前体细胞被激活并分化。(2) 吸收;破骨细胞通过去除骨基质和矿物质来吸收一定体积的骨。(3) 形成;成骨细胞分化并形成新骨。破骨细胞吸收和成骨细胞形成在空间和时间上的细胞偶联不仅受全身激素(雌激素、甲状旁腺激素、降钙素或维生素D等)和局部因子(转化生长因子-β、骨形态发生蛋白、胰岛素样生长因子、前列腺素、白细胞介素或肿瘤坏死因子-α等)的调节,还受机械应力的调节。我们综述了骨重塑的各种调节因子,并对骨重塑的调节机制进行了评论。