Wilson Nicole H, Key Brian
Discipline of Anatomy and Developmental Biology, School of Biomedical Sciences, The University of Queensland, Brisbane, Queensland 4072, Australia.
Dev Biol. 2006 Aug 15;296(2):485-98. doi: 10.1016/j.ydbio.2006.06.018. Epub 2006 Jun 15.
In the embryonic forebrain, pioneer axons establish a simple topography of dorsoventral and longitudinal tracts. The cues used by these axons during the initial formation of the axon scaffold remain largely unknown. We have investigated the axon guidance role of Neogenin, a member of the immunoglobulin (Ig) superfamily that binds to the chemoattractive ligand Netrin-1, as well as to the chemorepulsive ligand repulsive guidance molecule (RGMa). Here, we show strong expression of Neogenin and both of its putative ligands in the developing Xenopus forebrain. Neogenin loss-of-function mutants revealed that this receptor was essential for axon guidance in an early forming dorsoventral brain pathway. Similar mutant phenotypes were also observed following loss of either RGMa or Netrin-1. Simultaneous partial knock downs of these molecules revealed dosage-sensitive interactions and confirmed that these receptors and ligands were acting in the same pathway. The results provide the first evidence that Neogenin acts as an axon guidance molecule in vivo and support a model whereby Neogenin-expressing axons respond to a combination of attractive and repulsive cues as they navigate their ventral trajectory.
在胚胎前脑中,先驱轴突建立起背腹侧和纵向束的简单拓扑结构。这些轴突在轴突支架最初形成过程中所使用的线索在很大程度上仍不为人知。我们研究了Neogenin的轴突导向作用,Neogenin是免疫球蛋白(Ig)超家族的成员,它既能与化学吸引配体Netrin-1结合,也能与化学排斥配体排斥导向分子(RGMa)结合。在此,我们展示了Neogenin及其两种假定配体在发育中的非洲爪蟾前脑中的强烈表达。Neogenin功能丧失突变体表明,该受体对于早期形成的背腹侧脑通路中的轴突导向至关重要。在RGMa或Netrin-1缺失后也观察到了类似的突变体表型。同时对这些分子进行部分敲低显示出剂量敏感的相互作用,并证实这些受体和配体在同一通路中起作用。这些结果提供了首个证据,表明Neogenin在体内作为轴突导向分子发挥作用,并支持这样一种模型,即表达Neogenin的轴突在沿着其腹侧轨迹导航时对吸引和排斥线索的组合做出反应。