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Live imaging of retinotectal mapping reveals topographic map dynamics and a previously undescribed role for Contactin 2 in map sharpening.视网膜-顶盖投射图的实时成像揭示了地形图动态以及 Contactin 2 在图锐化中以前未被描述的作用。
Development. 2021 Nov 15;148(22). doi: 10.1242/dev.199584.
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Retinotectal circuitry of larval zebrafish is adapted to detection and pursuit of prey.幼鱼的视网膜-顶盖电路适应于对猎物的检测和追逐。
Elife. 2020 Oct 12;9:e58596. doi: 10.7554/eLife.58596.
2
cAMP-Dependent Co-stabilization of Axonal Arbors from Adjacent Developing Neurons.cAMP 依赖性共稳定来自相邻发育神经元的轴突树突。
Cell Rep. 2020 Oct 6;33(1):108220. doi: 10.1016/j.celrep.2020.108220.
3
Cell Types of the Human Retina and Its Organoids at Single-Cell Resolution.人类视网膜及其类器官的细胞类型解析
Cell. 2020 Sep 17;182(6):1623-1640.e34. doi: 10.1016/j.cell.2020.08.013.
4
Trans-Axonal Signaling in Neural Circuit Wiring.轴突转导在神经回路连接中的作用
Int J Mol Sci. 2020 Jul 21;21(14):5170. doi: 10.3390/ijms21145170.
5
Stentian structural plasticity in the developing visual system.发育中的视觉系统中的支架式结构可塑性。
Proc Natl Acad Sci U S A. 2020 May 19;117(20):10636-10638. doi: 10.1073/pnas.2001107117. Epub 2020 May 4.
6
SuperPlots: Communicating reproducibility and variability in cell biology.超图:展示细胞生物学中的可重复性和可变性。
J Cell Biol. 2020 Jun 1;219(6). doi: 10.1083/jcb.202001064.
7
TAG-1 Multifunctionality Coordinates Neuronal Migration, Axon Guidance, and Fasciculation.TAG-1 多功能性协调神经元迁移、轴突导向和纤维形成。
Cell Rep. 2020 Jan 28;30(4):1164-1177.e7. doi: 10.1016/j.celrep.2019.12.085.
8
Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish.高效的基于 CRISPR-Cas9 的方法用于生成缺失突变和缺乏基因功能的 F0 胚胎在斑马鱼中。
Dev Cell. 2019 Dec 2;51(5):645-657.e4. doi: 10.1016/j.devcel.2019.10.004. Epub 2019 Nov 7.
9
A single-cell transcriptome atlas of the adult human retina.成人视网膜单细胞转录组图谱。
EMBO J. 2019 Sep 16;38(18):e100811. doi: 10.15252/embj.2018100811. Epub 2019 Aug 22.
10
Optic nerve regeneration in larval zebrafish exhibits spontaneous capacity for retinotopic but not tectum specific axon targeting.幼虫斑马鱼的视神经再生表现出视网膜层定位的自发能力,但没有顶盖结构特异性的轴突靶向。
PLoS One. 2019 Jun 20;14(6):e0218667. doi: 10.1371/journal.pone.0218667. eCollection 2019.

视网膜-顶盖投射图的实时成像揭示了地形图动态以及 Contactin 2 在图锐化中以前未被描述的作用。

Live imaging of retinotectal mapping reveals topographic map dynamics and a previously undescribed role for Contactin 2 in map sharpening.

机构信息

Department of Biological Sciences, University of South Carolina, Columbia, SC 29208, USA.

出版信息

Development. 2021 Nov 15;148(22). doi: 10.1242/dev.199584.

DOI:10.1242/dev.199584
PMID:34698769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8645211/
Abstract

Organization of neuronal connections into topographic maps is essential for processing information. Yet, our understanding of topographic mapping has remained limited by our inability to observe maps forming and refining directly in vivo. Here, we used Cre-mediated recombination of a new colorswitch reporter in zebrafish to generate the first transgenic model allowing the dynamic analysis of retinotectal mapping in vivo. We found that the antero-posterior retinotopic map forms early but remains dynamic, with nasal and temporal retinal axons expanding their projection domains over time. Nasal projections initially arborize in the anterior tectum but progressively refine their projection domain to the posterior tectum, leading to the sharpening of the retinotopic map along the antero-posterior axis. Finally, using a CRISPR-mediated mutagenesis approach, we demonstrate that the refinement of nasal retinal projections requires the adhesion molecule Contactin 2. Altogether, our study provides the first analysis of a topographic map maturing in real time in a live animal and opens new strategies for dissecting the molecular mechanisms underlying precise topographic mapping in vertebrates.

摘要

神经元连接的拓扑组织对于信息处理至关重要。然而,由于我们无法直接在体内观察到地图的形成和细化,我们对拓扑映射的理解仍然有限。在这里,我们使用斑马鱼中的一种新的颜色开关报告基因的 Cre 介导重组,生成了第一个允许在体内动态分析视网膜-顶盖映射的转基因模型。我们发现,前-后视网膜拓扑图形成得较早,但仍然具有动态性,鼻侧和颞侧视网膜轴突随着时间的推移扩展其投射区域。鼻侧投射最初在顶盖的前区分支,但随着时间的推移逐渐细化其投射区域到顶盖的后区,导致沿着前后轴的视网膜拓扑图的锐化。最后,我们使用 CRISPR 介导的诱变方法证明,鼻侧视网膜投射的细化需要黏附分子 Contactin 2。总之,我们的研究提供了在活体动物中实时成熟的拓扑图的首次分析,并为解析脊椎动物中精确拓扑映射的分子机制开辟了新的策略。