Runx2 inhibits chondrocyte proliferation and hypertrophy through its expression in the perichondrium

被引:133
作者
Hinoi, Eiichi
Bialek, Peter
Chen, You-Tzung
Rached, Marie-Therese
Groner, Yoram
Behringer, Richard R.
Ornitz, David M.
Karsenty, Gerard [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
[4] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[5] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
关键词
Twist-1; Runx2; FGF18; perichondrium; chondrocyte maturation;
D O I
10.1101/gad.1482906
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The perichondrium, a structure made of undifferentiated mesenchymal cells surrounding growth plate cartilage, regulates chondrocyte maturation through poorly understood mechanisms. Analyses of loss- and gain-of-function models show that Twist-1, whose expression in cartilage is restricted to perichondrium, favors chondrocyte maturation in a Runx2-dependent manner. Runx2, in turn, enhances perichondrial expression of Fgf18, a regulator of chondrocyte maturation. Accordingly, compound heterozygous embryos for Runx2 and Fgf18 deletion display the same chondrocyte maturation phenotype as Fgf18-null embryos. This study identifies a transcriptional basis for the inhibition of chondrocyte maturation by perichondrium and reveals that Runx2 fulfills antagonistic functions during chondrogenesis.
引用
收藏
页码:2937 / 2942
页数:6
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