Hung Irene H, Yu Kai, Lavine Kory J, Ornitz David M
Department of Molecular Biology and Pharmacology, Washington University School of Medicine, Campus Box 8103, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
Dev Biol. 2007 Jul 15;307(2):300-13. doi: 10.1016/j.ydbio.2007.04.048. Epub 2007 May 6.
Gain-of-function mutations in fibroblast growth factor (FGF) receptors result in chondrodysplasia and craniosynostosis syndromes, highlighting the critical role for FGF signaling in skeletal development. Although the FGFRs involved in skeletal development have been well characterized, only a single FGF ligand, FGF18, has been identified that regulates skeletal development during embryogenesis. Here we identify Fgf9 as a second FGF ligand that is critical for skeletal development. We show that Fgf9 is expressed in the proximity of developing skeletal elements and that Fgf9-deficient mice exhibit rhizomelia (a disproportionate shortening of proximal skeletal elements), which is a prominent feature of patients with FGFR3-induced chondrodysplasia syndromes. Although Fgf9 is expressed in the apical ectodermal ridge in the limb bud, we demonstrate that the Fgf9-/- limb phenotype results from loss of FGF9 functions after formation of the mesenchymal condensation. In developing stylopod elements, FGF9 promotes chondrocyte hypertrophy at early stages and regulates vascularization of the growth plate and osteogenesis at later stages of skeletal development.
成纤维细胞生长因子(FGF)受体的功能获得性突变会导致软骨发育不全和颅缝早闭综合征,这凸显了FGF信号在骨骼发育中的关键作用。尽管参与骨骼发育的FGFR已得到充分表征,但在胚胎发育过程中,仅鉴定出一种调节骨骼发育的FGF配体——FGF18。在此,我们确定Fgf9是对骨骼发育至关重要的第二种FGF配体。我们发现Fgf9在发育中的骨骼元件附近表达,且Fgf9基因敲除小鼠表现出肢根短小(近端骨骼元件不成比例地缩短),这是FGFR3诱导的软骨发育不全综合征患者的一个显著特征。尽管Fgf9在肢芽的顶端外胚层嵴中表达,但我们证明Fgf9基因敲除小鼠的肢体表型是由于间充质凝聚形成后FGF9功能丧失所致。在发育中的上肢骨元件中,FGF9在早期促进软骨细胞肥大,并在骨骼发育后期调节生长板的血管生成和成骨作用。