破骨细胞
兰克尔
成骨细胞
细胞生物学
化学
骨重建
细胞分化
信号转导
内分泌学
生物
受体
激活剂(遗传学)
体外
生物化学
基因
作者
Jung‐Min Kim,Chujiao Lin,Zheni Stavre,Matthew B. Greenblatt,Jae‐Hyuck Shim
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2020-09-10
卷期号:9 (9): 2073-2073
被引量:689
摘要
Bone remodeling is tightly regulated by a cross-talk between bone-forming osteoblasts and bone-resorbing osteoclasts. Osteoblasts and osteoclasts communicate with each other to regulate cellular behavior, survival and differentiation through direct cell-to-cell contact or through secretory proteins. A direct interaction between osteoblasts and osteoclasts allows bidirectional transduction of activation signals through EFNB2-EPHB4, FASL-FAS or SEMA3A-NRP1, regulating differentiation and survival of osteoblasts or osteoclasts. Alternatively, osteoblasts produce a range of different secretory molecules, including M-CSF, RANKL/OPG, WNT5A, and WNT16, that promote or suppress osteoclast differentiation and development. Osteoclasts also influence osteoblast formation and differentiation through secretion of soluble factors, including S1P, SEMA4D, CTHRC1 and C3. Here we review the current knowledge regarding membrane bound- and soluble factors governing cross-talk between osteoblasts and osteoclasts.
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