Chance Rebecca K, Bashaw Greg J
Department of Neuroscience, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
PLoS Genet. 2015 Sep 3;11(9):e1005402. doi: 10.1371/journal.pgen.1005402. eCollection 2015 Sep.
Understanding how axon guidance receptors are activated by their extracellular ligands to regulate growth cone motility is critical to learning how proper wiring is established during development. Roundabout (Robo) is one such guidance receptor that mediates repulsion from its ligand Slit in both invertebrates and vertebrates. Here we show that endocytic trafficking of the Robo receptor in response to Slit-binding is necessary for its repulsive signaling output. Dose-dependent genetic interactions and in vitro Robo activation assays support a role for Clathrin-dependent endocytosis, and entry into both the early and late endosomes as positive regulators of Slit-Robo signaling. We identify two conserved motifs in Robo's cytoplasmic domain that are required for its Clathrin-dependent endocytosis and activation in vitro; gain of function and genetic rescue experiments provide strong evidence that these trafficking events are required for Robo repulsive guidance activity in vivo. Our data support a model in which Robo's ligand-dependent internalization from the cell surface to the late endosome is essential for receptor activation and proper repulsive guidance at the midline by allowing recruitment of the downstream effector Son of Sevenless in a spatially constrained endocytic trafficking compartment.
了解轴突导向受体如何被其细胞外配体激活以调节生长锥运动,对于理解发育过程中如何建立正确的神经连接至关重要。Roundabout(Robo)就是这样一种导向受体,它在无脊椎动物和脊椎动物中均介导对其配体Slit的排斥反应。在此,我们表明Robo受体响应Slit结合的内吞运输对于其排斥信号输出是必要的。剂量依赖性遗传相互作用和体外Robo激活试验支持网格蛋白依赖性内吞作用以及进入早期和晚期内体作为Slit-Robo信号的正向调节因子发挥作用。我们在Robo的胞质结构域中鉴定出两个保守基序,它们是其网格蛋白依赖性内吞作用和体外激活所必需的;功能获得和基因拯救实验提供了强有力的证据,表明这些运输事件是Robo在体内排斥导向活性所必需的。我们的数据支持一种模型,其中Robo从细胞表面到晚期内体的配体依赖性内化对于受体激活以及通过在空间受限的内吞运输区室中招募下游效应器Sevenless之子在中线进行适当的排斥导向至关重要。