Lu Pengfei, Yu Ying, Perdue Yasmine, Werb Zena
Department of Anatomy and Program in Developmental Biology, University of California at San Francisco, San Francisco, CA 94143-0452, USA.
Development. 2008 Apr;135(8):1395-405. doi: 10.1242/dev.018945.
The apical ectodermal ridge (AER) is a transient embryonic structure essential for the induction, patterning and outgrowth of the vertebrate limb. However, the mechanism of AER function in limb skeletal patterning has remained unclear. In this study, we genetically ablated the AER by conditionally removing FGFR2 function and found that distal limb development failed in mutant mice. We showed that FGFR2 promotes survival of AER cells and interacts with Wnt/beta-catenin signaling during AER maintenance. Interestingly, cell proliferation and survival were not significantly reduced in the distal mesenchyme of mutant limb buds. We established Hoxa13 expression as an early marker of distal limb progenitors and discovered a dynamic morphogenetic process of distal limb development. We found that premature AER loss in mutant limb buds delayed generation of autopod progenitors, which in turn failed to reach a threshold number required to form a normal autopod. Taken together, we have uncovered a novel mechanism, whereby the AER regulates the number of autopod progenitors by determining the onset of their generation.
顶端外胚层嵴(AER)是一种短暂的胚胎结构,对脊椎动物肢体的诱导、模式形成和生长至关重要。然而,AER在肢体骨骼模式形成中的功能机制仍不清楚。在本研究中,我们通过条件性去除FGFR2功能对AER进行基因消融,发现突变小鼠的远端肢体发育失败。我们表明,FGFR2促进AER细胞的存活,并在AER维持过程中与Wnt/β-连环蛋白信号相互作用。有趣的是,突变肢体芽远端间充质中的细胞增殖和存活并未显著降低。我们将Hoxa13表达确立为远端肢体祖细胞的早期标志物,并发现了远端肢体发育的动态形态发生过程。我们发现,突变肢体芽中AER的过早缺失延迟了 autopod 祖细胞的产生,而这些祖细胞又未能达到形成正常 autopod 所需的阈值数量。综上所述,我们揭示了一种新机制,即AER通过确定autopod祖细胞产生的起始来调节其数量。