Takahashi Naoyuki
Matsumoto Dental University, Division of Hard Tissue Research, Institute for Oral Science.
Clin Calcium. 2006 Jun;16(6):940-47.
Osteoclast differentiation is tightly regulated by osteoblasts. Osteoblasts express two cytokines, macrophage colony-stimulating factor (M-CSF) and receptor activator of NF-kappaB ligand (RANKL), essential for osteoclast differentiation. Osteoclast precursors firstly differentiate into mononuclear osteoclasts in response to M-CSF and RANKL. Nuclear factor of activated T cells 1 (NFATc1) is a transcription factor, which is involved in the determination of osteoclast differentiation. The mononuclear osteoclast then fuses each other to form the multinucleated cell. Dendritic cell-specific transmembrane protein (DC-STAMP) plays an important role in the fusion of mononuclear osteoclasts. Osteoclasts recognize bone and form ruffled borders and clear zones on the bone surface (polarization). Polarizing osteoclasts construct active vascular transportation systems to resorb bone efficiently. RANK-TRAF6 (TNF receptor-associated factor 6) -mediated signals key roles in both osteoclast differentiation and function. In this article, I will review the recent findings on osteoclast differentiation and function.
破骨细胞的分化受到成骨细胞的严格调控。成骨细胞表达两种细胞因子,即巨噬细胞集落刺激因子(M-CSF)和核因子κB受体激活剂配体(RANKL),它们对破骨细胞的分化至关重要。破骨细胞前体细胞首先在M-CSF和RANKL的作用下分化为单核破骨细胞。活化T细胞核因子1(NFATc1)是一种转录因子,参与破骨细胞分化的决定过程。单核破骨细胞随后相互融合形成多核细胞。树突状细胞特异性跨膜蛋白(DC-STAMP)在单核破骨细胞的融合过程中起重要作用。破骨细胞识别骨组织,并在骨表面形成褶皱缘和清亮区(极化)。极化的破骨细胞构建活跃的血管运输系统以有效地吸收骨组织。RANK-TRAF6(肿瘤坏死因子受体相关因子6)介导的信号在破骨细胞的分化和功能中均起关键作用。在本文中,我将综述破骨细胞分化和功能方面的最新研究发现。