钙粘蛋白-6通过整合素介导的途径控制小鼠新皮质发育过程中的神经元迁移。

Yuki Hirota, Rikaho Saito, Takao Honda, Hitomi Sano, Mayuko Hotta, Yukiko U Inoue, Takayoshi Inoue, Kazunori Nakajima
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引用次数: 0

摘要

在新皮层发育过程中,神经元迁移受到多种信号级联反应的高度调控,包括细胞粘附分子。钙粘蛋白-6 (cadherin -6, CDH6)是一种罕见的钙粘蛋白分子,含有RGD整合素结合基序,在发育中的神经系统中具有多种功能,但它是否有助于新皮层发育过程中的神经元迁移和定位尚不清楚。在这里,我们研究了CDH6在发育中的大脑皮层中的作用。子宫电穿孔Cdh6敲除(KD)结果显示,Cdh6抑制导致神经元径向迁移受损和定位异常。延时成像分析显示CDH6对正常的神经元运动很重要。在机制上,我们发现CDH6促进迁移神经元上整合素β1的激活。整合素β1的适度过表达和野生型Cdh6的抗KD形式可以修复由Cdh6 KD引起的神经元迁移缺陷,而带有突变RGD基序的Cdh6则不能。这些结果表明CDH6是皮质兴奋性神经元通过控制整合素介导的细胞运动进行径向迁移所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cadherin-6 controls neuronal migration during mouse neocortical development via an integrin-mediated pathway.

During neocortical development, neuronal migration is highly regulated by multiple signaling cascades, including the cell adhesion molecules. Cadherin-6 (CDH6), an unusual cadherin molecule containing an RGD integrin-binding motif, has multiple functions in the developing nervous system, but whether it contributes to neuronal migration and positioning during neocortical development remains unknown. Here, we investigated the role of CDH6 in the developing cerebral cortex. Cdh6 knockdown (KD) using in utero electroporation revealed that CDH6 inhibition caused impaired radial migration and abnormal positioning of neurons. Time-lapse imaging analysis revealed that CDH6 is important for proper neuronal motility. Mechanistically, we show that CDH6 promotes the activation of integrin β1 on migrating neurons. The defect in neuronal migration caused by Cdh6 KD was rescued by moderate overexpression of integrin β1 and a KD-resistant form of wild-type CDH6, but not by CDH6 with a mutated RGD motif. These results suggest that CDH6 is required for cortical excitatory neurons to migrate radially by controlling integrin-mediated cell motility.

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