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Development of the Endochondral Skeleton
Author(s) -
Fanxin Long,
David M. Ornitz
Publication year - 2013
Publication title -
cold spring harbor perspectives in biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.011
H-Index - 173
ISSN - 1943-0264
DOI - 10.1101/cshperspect.a008334
Subject(s) - endochondral ossification , chondrocyte , runx2 , biology , microbiology and biotechnology , cartilage , sox9 , osteoblast , intramembranous ossification , transcription factor , chondrogenesis , fibroblast growth factor , anatomy , receptor , genetics , gene , in vitro
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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