Department of Cell Biology, Physiology and Immunology, Faculty of Biology and Institute of Neurosciences, University of Barcelona, Barcelona, Spain.
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII, Madrid, Spain.
PLoS Genet. 2018 Jun 18;14(6):e1007432. doi: 10.1371/journal.pgen.1007432. eCollection 2018 Jun.
Axonal growth and guidance rely on correct growth cone responses to guidance cues. Unlike the signaling cascades that link axonal growth to cytoskeletal dynamics, little is known about the crosstalk mechanisms between guidance and membrane dynamics and turnover. Recent studies indicate that whereas axonal attraction requires exocytosis, chemorepulsion relies on endocytosis. Indeed, our own studies have shown that Netrin-1/Deleted in Colorectal Cancer (DCC) signaling triggers exocytosis through the SNARE Syntaxin-1 (STX1). However, limited in vivo evidence is available about the role of SNARE proteins in axonal guidance. To address this issue, here we systematically deleted SNARE genes in three species. We show that loss-of-function of STX1 results in pre- and post-commissural axonal guidance defects in the midline of fly, chick, and mouse embryos. Inactivation of VAMP2, Ti-VAMP, and SNAP25 led to additional abnormalities in axonal guidance. We also confirmed that STX1 loss-of-function results in reduced sensitivity of commissural axons to Slit-2 and Netrin-1. Finally, genetic interaction studies in Drosophila show that STX1 interacts with both the Netrin-1/DCC and Robo/Slit pathways. Our data provide evidence of an evolutionarily conserved role of STX1 and SNARE proteins in midline axonal guidance in vivo, by regulating both pre- and post-commissural guidance mechanisms.
轴突生长和导向依赖于正确的生长锥对导向线索的反应。与将轴突生长与细胞骨架动力学联系起来的信号级联不同,关于导向与膜动力学和周转率之间的串扰机制知之甚少。最近的研究表明,虽然轴突吸引需要胞吐作用,但趋化排斥依赖于胞吞作用。事实上,我们自己的研究表明,Netrin-1/结直肠癌缺失(DCC)信号通过 SNARE 突触融合蛋白 1(STX1)触发胞吐作用。然而,关于 SNARE 蛋白在轴突导向中的作用,体内证据有限。为了解决这个问题,我们在这里在三个物种中系统地删除了 SNARE 基因。我们表明,STX1 的功能丧失会导致果蝇、鸡和鼠胚胎中线的前和后连合轴突导向缺陷。VAMP2、Ti-VAMP 和 SNAP25 的失活导致轴突导向的额外异常。我们还证实 STX1 的功能丧失会导致连合轴突对 Slit-2 和 Netrin-1 的敏感性降低。最后,果蝇中的遗传相互作用研究表明,STX1 与 Netrin-1/DCC 和 Robo/Slit 途径相互作用。我们的数据提供了 STX1 和 SNARE 蛋白在体内中线轴突导向中具有保守作用的证据,通过调节前和后连合导向机制。