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利用新型 Robo3 小鼠进行基因标记和分子分析揭示了多样化的脊髓连合神经元群体。

Diverse spinal commissural neuron populations revealed by fate mapping and molecular profiling using a novel Robo3 mouse.

机构信息

Department of Neuroscience, Brown University, Providence, Rhode Island.

Robert J. and Nancy D. Carney Institute for Brain Science, Providence, Rhode Island.

出版信息

J Comp Neurol. 2019 Dec 15;527(18):2948-2972. doi: 10.1002/cne.24720. Epub 2019 Jun 14.

DOI:10.1002/cne.24720
PMID:31152445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6790177/
Abstract

The two sides of the nervous system coordinate and integrate information via commissural neurons, which project axons across the midline. Commissural neurons in the spinal cord are a highly heterogeneous population of cells with respect to their birthplace, final cell body position, axonal trajectory, and neurotransmitter phenotype. Although commissural axon guidance during development has been studied in great detail, neither the developmental origins nor the mature phenotypes of commissural neurons have been characterized comprehensively, largely due to lack of selective genetic access to these neurons. Here, we generated mice expressing Cre recombinase from the Robo3 locus specifically in commissural neurons. We used Robo3 mice to characterize the transcriptome and various origins of developing commissural neurons, revealing new details about their extensive heterogeneity in molecular makeup and developmental lineage. Further, we followed the fate of commissural neurons into adulthood, thereby elucidating their settling positions and molecular diversity and providing evidence for possible functions in various spinal cord circuits. Our studies establish an important genetic entry point for further analyses of commissural neuron development, connectivity, and function.

摘要

神经系统的两侧通过连合神经元协调和整合信息,这些神经元的轴突穿过中线投射。脊髓中的连合神经元在出生地、最终细胞体位置、轴突轨迹和神经递质表型方面具有高度异质性。尽管在发育过程中已经对连合轴突的导向进行了详细研究,但连合神经元的发育起源和成熟表型尚未得到全面描述,主要是由于缺乏对这些神经元的选择性遗传方法。在这里,我们生成了在连合神经元中特异性表达 Cre 重组酶的 Robo3 基因敲入小鼠。我们使用 Robo3 小鼠来描述发育中的连合神经元的转录组和各种起源,揭示了它们在分子组成和发育谱系上广泛异质性的新细节。此外,我们还跟踪了连合神经元进入成年期的命运,从而阐明了它们的定居位置和分子多样性,并为它们在各种脊髓回路中的可能功能提供了证据。我们的研究为进一步分析连合神经元的发育、连接和功能建立了一个重要的遗传切入点。

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本文引用的文献

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J Comp Neurol. 2018 Aug 15;526(12):1943-1961. doi: 10.1002/cne.24464.
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DNER modulates the length, polarity and synaptogenesis of spiral ganglion neurons via the Notch signaling pathway.DNER 通过 Notch 信号通路调节螺旋神经节神经元的长度、极性和突触形成。
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Regulation of the Hippocampal Network by VGLUT3-Positive CCK- GABAergic Basket Cells.VGLUT3阳性CCK-γ-氨基丁酸能篮状细胞对海马网络的调节
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