软骨内骨化
生物
细胞生物学
软骨
软骨细胞
骨化
胚胎干细胞
Wnt信号通路
解剖
连环素
连环蛋白
兰克尔
骨重建
内分泌学
内科学
信号转导
基因
激活剂(遗传学)
遗传学
医学
作者
Astrid Houben,Daniela Kostanova‐Poliakova,Martina Weißenböck,Julian Graf,Stefan Teufel,Klaus von der Mark,Christine Hartmann
出处
期刊:Development
[The Company of Biologists]
日期:2016-09-13
卷期号:143 (20): 3826-3838
被引量:76
摘要
Trabecular bone formation is the last step in endochondral ossification. This remodeling process of cartilage into bone involves blood vessel invasion and removal of hypertrophic chondrocytes (HTCs) by chondroclasts and osteoclasts. Periosteal- and chondrocyte-derived osteoprogenitors utilize the leftover mineralized HTC matrix as a scaffold for primary spongiosa formation. Here, we show genetically that β-catenin (encoded by Ctnnb1), a key component of the canonical Wnt pathway, orchestrates this remodeling process at multiple levels. Conditional inactivation or stabilization of β-catenin in HTCs by a Col10a1-Cre line locally modulated osteoclastogenesis by altering the Rankl:Opg ratio in HTCs. Lack of β-catenin resulted in a severe decrease of trabecular bone in the embryonic long bones. Gain of β-catenin activity interfered with removal of late HTCs and bone marrow formation, leading to a continuous mineralized hypertrophic core in the embryo and resulting in an osteopetrotic-like phenotype in adult mice. Furthermore, β-catenin activity in late HTCs is required for chondrocyte-derived osteoblastogenesis at the chondro-osseous junction. The latter contributes to the severe trabecular bone phenotype in mutants lacking β-catenin activity in HTCs.
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