软骨内骨化
软骨细胞
运行x2
生物
细胞生物学
软骨
硫氧化物9
成骨细胞
膜内骨化
转录因子
软骨发生
成纤维细胞生长因子
解剖
受体
遗传学
体外
基因
作者
Fanxin Long,David M. Ornitz
标识
DOI:10.1101/cshperspect.a008334
摘要
Much of the mammalian skeleton is composed of bones that originate from cartilage templates through endochondral ossification. Elucidating the mechanisms that control endochondral bone development is critical for understanding human skeletal diseases, injury response, and aging. Mouse genetic studies in the past 15 years have provided unprecedented insights about molecules regulating chondrocyte formation, chondrocyte maturation, and osteoblast differentiation, all key processes of endochondral bone development. These include the roles of the secreted proteins IHH, PTHrP, BMPs, WNTs, and FGFs, their receptors, and transcription factors such as SOX9, RUNX2, and OSX, in regulating chondrocyte and osteoblast biology. This review aims to integrate the known functions of extracellular signals and transcription factors that regulate development of the endochondral skeleton.
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