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信号素6A-丛状蛋白A2/A4与放射状胶质细胞的相互作用调节表层皮质神经元的迁移终止

Semaphorin 6A-Plexin A2/A4 Interactions with Radial Glia Regulate Migration Termination of Superficial Layer Cortical Neurons.

作者信息

Hatanaka Yumiko, Kawasaki Takahiko, Abe Takaya, Shioi Go, Kohno Takao, Hattori Mitsuharu, Sakakibara Akira, Kawaguchi Yasuo, Hirata Tatsumi

机构信息

Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan; Division of Cerebral Circuitry, National Institute for Physiological Sciences, 5-1 Higashiyama, Myodaiji, Okazaki, Aichi 444-8787, Japan; College of Life and Health Sciences, Chubu University, 1200 Matsumoto-cho, Kasugai, Aichi 487-8501, Japan.

Brain Function Laboratory, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

出版信息

iScience. 2019 Nov 22;21:359-374. doi: 10.1016/j.isci.2019.10.034. Epub 2019 Oct 21.

Abstract

Precise regulation of neuronal migration termination is crucial for the establishment of brain cytoarchitectures. However, little is known about how neurons terminate migration. Here we focused on interactions between migrating cortical neurons and their substrates, radial glial (RG) cells, and analyzed the role of Plexin A2 and A4 (PlxnA2/A4) receptors and their repulsive ligand, Semaphorin 6A (Sema6A), for this process. In both PlxnA2/A4 double-knockout and Sema6A mutant mice, the outermost cortical plate neurons ectopically invade layer 1 at a stage when they should reach their destinations. PlxnA2/A4 proteins are abundantly expressed on their leading processes, whereas Sema6A mRNA is enriched in RG cell somata. Cell-targeted gene expression and conditional knockouts indicate critical roles for these molecules. We hypothesize that the timely appearance of repulsive signaling mediated by Sema6A-PlxnA2/A4 weakens migrating neuron-RG cell interactions, leading to migration termination.

摘要

神经元迁移终止的精确调控对于脑 cytoarchitecture 的建立至关重要。然而,关于神经元如何终止迁移却知之甚少。在这里,我们聚焦于迁移的皮质神经元与其底物——放射状胶质(RG)细胞之间的相互作用,并分析了 Plexin A2 和 A4(PlxnA2/A4)受体及其排斥性配体 Semaphorin 6A(Sema6A)在此过程中的作用。在 PlxnA2/A4 双敲除小鼠和 Sema6A 突变小鼠中,最外层皮质板神经元在本应到达目的地的阶段异位侵入第 1 层。PlxnA2/A4 蛋白在其前端大量表达,而 Sema6A mRNA 在 RG 细胞胞体中富集。细胞靶向基因表达和条件性敲除表明这些分子具有关键作用。我们推测,由 Sema6A-PlxnA2/A4 介导的排斥信号的适时出现会削弱迁移神经元与 RG 细胞之间的相互作用,从而导致迁移终止。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49e1/6889767/d3390853b64d/fx1.jpg

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