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

E Hinoi, P Bialek, YT Chen, MT Rached… - Genes & …, 2006 - genesdev.cshlp.org
E Hinoi, P Bialek, YT Chen, MT Rached, Y Groner, RR Behringer, DM Ornitz, G Karsenty
Genes & development, 2006genesdev.cshlp.org
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 …
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.
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