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A requirement for filopodia extension toward Slit during Robo-mediated axon repulsion

机译:在Robo介导的轴突排斥期间丝状伪足向slit延伸的要求

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摘要

Axons navigate long distances through complex 3D environments to interconnect the nervous system during development. Although the precise spatiotemporal effects of most axon guidance cues remain poorly characterized, a prevailing model posits that attractive guidance cues stimulate actin polymerization in neuronal growth cones whereas repulsive cues induce actin disassembly. Contrary to this model, we find that the repulsive guidance cue Slit stimulates the formation and elongation of actin-based filopodia from mouse dorsal root ganglion growth cones. Surprisingly, filopodia form and elongate toward sources of Slit, a response that we find is required for subsequent axonal repulsion away from Slit. Mechanistically, Slit evokes changes in filopodium dynamics by increasing direct binding of its receptor, Robo, to members of the actin-regulatory Ena/VASP family. Perturbing filopodium dynamics pharmacologically or genetically disrupts Slit-mediated repulsion and produces severe axon guidance defects in vivo. Thus, Slit locally stimulates directional filopodial extension, a process that is required for subsequent axonal repulsion downstream of the Robo receptor.
机译:轴突在复杂的3D环境中导航,以在开发过程中互连神经系统。尽管大多数轴突引导线索的精确时空效果仍然很差,但一种流行的模型认为有吸引力的引导线索会刺激神经元生长锥中的肌动蛋白聚合,而排斥性线索会导致肌动蛋白分解。与该模型相反,我们发现排斥指导线索Slit刺激了小鼠背根神经节生长锥的肌动蛋白丝状伪足的形成和伸长。出人意料的是,丝状伪足形成并向狭缝源延伸,我们发现,随后的轴突排斥力需要远离狭缝的反应。从机制上讲,Slit通过增加其受体Robo与肌动蛋白调节性Ena / VASP家族成员的直接结合,引发了拟po动力学的变化。药理或遗传上扰动假单胞菌动力学会破坏狭缝介导的排斥力,并在体内产生严重的轴突导向缺陷。因此,狭缝局部刺激定向的丝状伸展,这是随后在Robo受体下游轴突排斥所需的过程。

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