Ziak Jakub, Dorskind Joelle, Trigg Brian, Sudarsanam Sriram, Hand Randal, Kolodkin Alex L
The Solomon H. Snyder Department of Neuroscience, Johns Hopkins Kavli Neuroscience Discovery Institute, The Johns Hopkins School of Medicine, 725 North Wolfe St., Baltimore, MD 21205.
Novartis Institutes for BioMedical Research, Boston, MA.
bioRxiv. 2023 Oct 2:2023.10.02.560024. doi: 10.1101/2023.10.02.560024.
Regulation of directed axon guidance and branching during development is essential for the generation of neuronal networks. However, the molecular mechanisms that underlie interstitial axon branching in the mammalian brain remain unresolved. Here, we investigate interstitial axon branching using an approach for precise labeling of layer 2/3 callosal projection neurons (CPNs), allowing for quantitative analysis of axonal morphology at high acuity and also manipulation of gene expression in well-defined temporal windows. We find that the GSK3β serine/threonine kinase promotes interstitial axon branching in layer 2/3 CPNs by releasing MAP1B-mediated inhibition of axon branching. Further, we find that the tubulin tyrosination cycle is a key downstream component of GSK3β/MAP1B signaling. We propose that MAP1B functions as a brake on axon branching that can be released by GSK3β activation, regulating the tubulin code and thereby playing an integral role in sculpting cortical neuron axon morphology.
发育过程中定向轴突导向和分支的调控对于神经网络的形成至关重要。然而,哺乳动物大脑中轴突在间质内分支的分子机制仍未得到解决。在这里,我们使用一种精确标记第2/3层胼胝体投射神经元(CPN)的方法来研究轴突在间质内的分支,从而能够在高分辨率下对轴突形态进行定量分析,并在明确的时间窗口内操纵基因表达。我们发现,GSK3β丝氨酸/苏氨酸激酶通过解除MAP1B介导的对轴突分支的抑制作用,促进第2/3层CPN的轴突在间质内分支。此外,我们发现微管蛋白酪氨酸化循环是GSK3β/MAP1B信号传导的关键下游成分。我们提出,MAP1B作为轴突分支的制动器,可通过GSK3β激活而解除,调节微管蛋白编码,从而在塑造皮质神经元轴突形态中发挥不可或缺的作用。