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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.
Twist-Related Protein 1, Gene Expression Regulation, Developmental, Nuclear Proteins, Cell Differentiation, Core Binding Factor Alpha 1 Subunit, Mice, Mutant Strains, Fibroblast Growth Factors, Mesoderm, Mice, Chondrocytes, Animals, Growth Plate, Chondrogenesis, Gene Deletion, Cell Proliferation
Twist-Related Protein 1, Gene Expression Regulation, Developmental, Nuclear Proteins, Cell Differentiation, Core Binding Factor Alpha 1 Subunit, Mice, Mutant Strains, Fibroblast Growth Factors, Mesoderm, Mice, Chondrocytes, Animals, Growth Plate, Chondrogenesis, Gene Deletion, Cell Proliferation
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 144 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |