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The cell adhesion molecule NrCAM is crucial for growth cone behaviour and pathfinding of retinal ganglion cell axons.

机译:细胞粘附分子NrCAM对于视网膜神经节细胞轴突的生长锥行为和寻路至关重要。

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We investigated the role of the cell adhesion molecule NrCAM for axonal growth and pathfinding in the developing retina. Analysis of the distribution pattern of NrCAM in chick embryo retina sections and flat-mounts shows its presence during extension of retinal ganglion cell (RGC) axons; NrCAM is selectively present on RGC axons and is absent from the soma. Single cell cultures show an enrichment of NrCAM in the distal axon and growth cone. When offered as a substrate in addition to Laminin, NrCAM promotes RGC axon extension and the formation of growth cone protrusions. In substrate stripe assays, mimicking the NrCAM-displaying optic fibre layer and the Laminin-rich basal lamina, RGC axons preferentially grow on NrCAM lanes. The three-dimensional analysis of RGC growth cones in retina flat-mounts reveals that they are enlarged and form more protrusions extending away from the correct pathway under conditions of NrCAM-inhibition. Time-lapse analyses show that these growth cones pause longer to explore their environment, proceed for shorter time spans, and retract more often than under control conditions; in addition, they often deviate from the correct pathway towards the optic fissure. Inhibition of NrCAM in organ-cultured intact eyes causes RGC axons to misroute at the optic fissure; instead of diving into the optic nerve head, these axons cross onto the opposite side of the retina. Our results demonstrate a crucial role for NrCAM in the navigation of RGC axons in the developing retina towards the optic fissure, and also for pathfinding into the optic nerve.
机译:我们调查了细胞黏附分子NrCAM在发展中的视网膜轴突生长和寻路中的作用。对NrCAM在雏鸡胚胎视网膜切片和平坦支架中的分布模式的分析表明,它在视网膜神经节细胞(RGC)轴突延伸过程中存在。 NrCAM选择性存在于RGC轴突上,而在体细胞中则不存在。单细胞培养显示远端轴突和生长锥中NrCAM的富集。当作为层粘连蛋白的底物提供时,NrCAM会促进RGC轴突延伸和生长锥突起的形成。在底物条纹测定中,模仿显示NrCAM的光纤层和富含层粘连蛋白的基底层,RGC轴突优先在NrCAM泳道上生长。视网膜平坦安装中RGC生长锥的三维分析显示,它们在NrCAM抑制条件下被放大并形成更多的突起,这些突起远离正确的途径延伸。延时分析表明,与在控制条件下相比,这些生长锥停下来探索环境的时间更长,进行的时间跨度更短,并且收缩的频率更高。此外,它们通常偏离正确的路径,朝着光学裂隙。在器官培养的完整眼中抑制NrCAM会导致RGC轴突在视神经裂隙处错线;这些轴突不是跨入视神经头部,而是跨入视网膜的另一侧。我们的结果证明了NrCAM在视网膜RGC轴突向视神经裂隙的导航中以及在寻路到视神经中的关键作用。

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