Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Molecular and Cellular Biology Graduate Program and Medical Scientist Training Program, University of Washington, Seattle, WA 98195, USA.
Dev Cell. 2020 May 4;53(3):344-357.e5. doi: 10.1016/j.devcel.2020.03.017. Epub 2020 Apr 16.
Information flow through neural circuits often requires their organization into topographic maps in which the positions of cell bodies and synaptic targets correspond. To understand how topographic map development is controlled, we examine the mechanism underlying targeting of vagus motor axons to the pharyngeal arches in zebrafish. We reveal that retinoic acid organizes topography by specifying anterior-posterior identity in vagus motor neurons. We then show that chemoattractant signaling between Hgf and Met is required for vagus innervation of the pharyngeal arches. Finally, we find that retinoic acid controls the spatiotemporal dynamics of Hgf/Met signaling to coordinate axon targeting with the developmental progression of the pharyngeal arches and show that experimentally altering the timing of Hgf/Met signaling is sufficient to redirect axon targeting and disrupt the topographic map. These findings establish a mechanism of topographic map development in which the regulation of chemoattractant signaling in space and time guides axon targeting.
信息在神经回路中的流动通常需要它们组织成拓扑图,其中细胞体和突触靶位的位置相对应。为了了解拓扑图发展是如何被控制的,我们研究了控制迷走运动轴突投射到斑马鱼咽弓的机制。我们揭示了视黄酸通过在迷走运动神经元中指定前后身份来组织拓扑图。然后我们表明,HGF 和 Met 之间的趋化因子信号对于迷走神经支配咽弓是必需的。最后,我们发现视黄酸控制 Hgf/Met 信号的时空动力学,以协调与咽弓发育进程相关的轴突靶向,并表明实验改变 Hgf/Met 信号的时间足以重新引导轴突靶向并破坏拓扑图。这些发现建立了一种拓扑图发展的机制,其中趋化因子信号在空间和时间上的调节指导轴突靶向。