Department of Biological Sciences, University of Notre Dame, Notre Dame, IN, 46556, USA.
Center for Stem Cells and Regenerative Medicine, University of Notre Dame, Notre Dame, IN, 46556, USA.
Nat Commun. 2019 Feb 4;10(1):562. doi: 10.1038/s41467-019-08421-9.
Sensory axons must traverse a spinal cord glia limitans to connect the brain with the periphery. The fundamental mechanism of how these axons enter the spinal cord is still debatable; both Ramon y Cajal's battering ram hypothesis and a boundary cap model have been proposed. To distinguish between these hypotheses, we visualized the entry of pioneer axons into the dorsal root entry zone (DREZ) with time-lapse imaging in zebrafish. Here, we identify that DRG pioneer axons enter the DREZ before the arrival of neural crest cells at the DREZ. Instead, actin-rich invadopodia in the pioneer axon are necessary and sufficient for DREZ entry. Using photoactivable Rac1, we demonstrate cell-autonomous functioning of invasive structures in pioneer axon spinal entry. Together these data support the model that actin-rich invasion structures dynamically drive pioneer axon entry into the spinal cord, indicating that distinct pioneer and secondary events occur at the DREZ.
感觉轴突必须穿越脊髓神经胶质界,才能将大脑与外周连接起来。这些轴突如何进入脊髓的基本机制仍有争议;拉蒙·卡哈尔的冲击假说和边界帽模型都被提出了。为了区分这些假说,我们在斑马鱼中进行了延时成像,以观察先驱轴突进入背根入口区 (DREZ) 的情况。在这里,我们发现 DRG 先驱轴突在神经嵴细胞到达 DREZ 之前就进入了 DREZ。相反,先驱轴突中的富含肌动蛋白的入侵足是进入 DREZ 所必需和充分的。利用光活化 Rac1,我们证明了先驱轴突中侵入性结构的细胞自主功能。这些数据共同支持了这样一种模型,即富含肌动蛋白的入侵结构动态地驱动先驱轴突进入脊髓,表明在 DREZ 处发生了不同的先驱和次级事件。