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在神经元迁移过程中,Reelin信号是如何调节神经元细胞骨架的?

How does Reelin signaling regulate the neuronal cytoskeleton during migration?

作者信息

Chai Xuejun, Frotscher Michael

机构信息

Institute for Structural Neurobiology, Center for Molecular Neurobiology Hamburg (ZMNH) , Hamburg, Germany.

出版信息

Neurogenesis (Austin). 2016 Sep 29;3(1):e1242455. doi: 10.1080/23262133.2016.1242455. eCollection 2016.

Abstract

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.

摘要

神经元迁移是形成分层脑结构的关键步骤。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,我们总结了我们最近关于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结果和假说。通过与迁移神经元上的ApoER2受体结合,Reelin诱导向边缘区延伸的前端突起稳定,这涉及Dab1磷酸化、黏附分子表达、丝切蛋白磷酸化以及tau磷酸化的抑制。通过与VLDLR和整合素受体结合,Reelin与Lis1相互作用并诱导核转位,同时伴有磷酸化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。由此导致的Reelin减少促使神经元在边缘区停滞。

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