Reelin信号在迁移过程中如何调节神经元细胞骨架?

Neurogenesis (Austin, Tex.) Pub Date : 2016-09-29 eCollection Date: 2016-01-01 DOI:10.1080/23262133.2016.1242455
Xuejun Chai, Michael Frotscher
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引用次数: 26

摘要

神经元迁移是层状脑结构形成的重要步骤。在发育中的大脑皮层,锥体神经元向含有reelin的边缘区迁移。Reelin是一种由Cajal-Retzius细胞合成的细胞外基质蛋白。在这篇综述中,我们总结了最近关于Reelin如何通过作用于肌动蛋白和微管细胞骨架来调节神经元迁移的研究结果和假设。通过与迁移神经元上的ApoER2受体结合,Reelin诱导了向边缘区延伸的主要过程的稳定,包括Dab1磷酸化、粘附分子表达、cofilin磷酸化和tau磷酸化的抑制。Reelin通过与VLDLR和整合素受体结合,与Lis1相互作用,诱导核易位,并伴随磷酸化Dab1的泛素化。最终,Reelin诱导其受体聚集,导致Reelin/受体复合物(特别是VLDLR)的内吞作用。由此产生的Reelin减少有助于边缘区神经元的停止。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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How does Reelin signaling regulate the neuronal cytoskeleton during migration?

Neuronal migration is an essential step in the formation of laminated brain structures. In the developing cerebral cortex, pyramidal neurons migrate toward the Reelin-containing marginal zone. Reelin is an extracellular matrix protein synthesized by Cajal-Retzius cells. In this review, we summarize our recent results and hypotheses on how Reelin might regulate neuronal migration by acting on the actin and microtubule cytoskeleton. By binding to ApoER2 receptors on the migrating neurons, Reelin induces stabilization of the leading processes extending toward the marginal zone, which involves Dab1 phosphorylation, adhesion molecule expression, cofilin phosphorylation and inhibition of tau phosphorylation. By binding to VLDLR and integrin receptors, Reelin interacts with Lis1 and induces nuclear translocation, accompanied by the ubiquitination of phosphorylated Dab1. Eventually Reelin induces clustering of its receptors resulting in the endocytosis of a Reelin/receptor complex (particularly VLDLR). The resulting decrease in Reelin contributes to neuronal arrest at the marginal zone.

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