Yu Kai, Ornitz David M
Department of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110 USA.
Development. 2008 Feb;135(3):483-91. doi: 10.1242/dev.013268. Epub 2007 Dec 19.
Fibroblast growth factors (FGFs) are signals from the apical ectodermal ridge (AER) that are essential for limb pattern formation along the proximodistal (PD) axis. However, how patterning along the PD axis is regulated by AER-FGF signals remains controversial. To further explore the molecular mechanism of FGF functions during limb development, we conditionally inactivated fgf receptor 2 (Fgfr2) in the mouse AER to terminate all AER functions; for comparison, we inactivated both Fgfr1 and Fgfr2 in limb mesenchyme to block mesenchymal AER-FGF signaling. We also re-examined published data in which Fgf4 and Fgf8 were inactivated in the AER. We conclude that limb skeletal phenotypes resulting from loss of AER-FGF signals cannot simply be a consequence of excessive mesenchymal cell death, as suggested by previous studies, but also must be a consequence of reduced mesenchymal proliferation and a failure of mesenchymal differentiation, which occur following loss of both Fgf4 and Fgf8. We further conclude that chondrogenic primordia formation, marked by initial Sox9 expression in limb mesenchyme, is an essential component of the PD patterning process and that a key role for AER-FGF signaling is to facilitate SOX9 function and to ensure progressive establishment of chondrogenic primordia along the PD axis.
成纤维细胞生长因子(FGFs)是来自顶端外胚层嵴(AER)的信号,对于肢体沿近远轴(PD轴)的模式形成至关重要。然而,AER - FGF信号如何调节沿PD轴的模式形成仍存在争议。为了进一步探索FGF在肢体发育过程中的分子机制,我们有条件地使小鼠AER中的成纤维细胞生长因子受体2(Fgfr2)失活,以终止所有AER功能;作为比较,我们使肢体间充质中的Fgfr1和Fgfr2均失活,以阻断间充质AER - FGF信号传导。我们还重新审视了已发表的数据,其中Fgf4和Fgf8在AER中被失活。我们得出结论,AER - FGF信号缺失导致的肢体骨骼表型不能简单地像先前研究所表明的那样,仅仅是间充质细胞过度死亡的结果,还必定是间充质增殖减少和间充质分化失败的结果,这些发生在Fgf4和Fgf8均缺失之后。我们进一步得出结论,以肢体间充质中最初的Sox9表达为标志的软骨原基形成是PD模式形成过程的一个重要组成部分,并且AER - FGF信号传导的关键作用是促进SOX9功能,并确保软骨原基沿PD轴逐步建立。