Shah Bhavin, Lutter Daniela, Tsytsyura Yaroslav, Glyvuk Natalia, Sakakibara Akira, Klingauf Jürgen, Püschel Andreas W
Institut für Molekulare Zellbiologie, Westfälische Wilhelms-Universität, D-48149 Münster, Germany.
Cells-in-Motion Cluster of Excellence, University of Münster, D-48149 Münster, Germany.
Cereb Cortex. 2017 Feb 1;27(2):1253-1269. doi: 10.1093/cercor/bhv341.
During the development of the mammalian neocortex, the generation of neurons by neural progenitors and their migration to the final position are closely coordinated. The highly polarized radial glial cells (RGCs) serve both as progenitor cells to generate neurons and as support for the migration of these neurons. After their generation, neurons transiently assume a multipolar morphology before they polarize and begin their migration along the RGCs. Here, we show that Rap1 GTPases perform essential functions for cortical organization as master regulators of cell polarity. Conditional deletion of Rap1 GTPases leads to a complete loss of cortical lamination. In RGCs, Rap1 GTPases are required to maintain their polarized organization. In newborn neurons, the loss of Rap1 GTPases prevents the formation of axons and leading processes and thereby interferes with radial migration. Taken together, the loss of RGC and neuronal polarity results in the disruption of cortical organization.
在哺乳动物新皮层的发育过程中,神经祖细胞产生神经元以及这些神经元迁移到最终位置的过程紧密协调。高度极化的放射状胶质细胞(RGCs)既作为产生神经元的祖细胞,又为这些神经元的迁移提供支持。神经元产生后,在极化并开始沿RGCs迁移之前,会短暂呈现多极形态。在此,我们表明Rap1 GTP酶作为细胞极性的主要调节因子,对皮层组织发挥着至关重要的作用。Rap1 GTP酶的条件性缺失导致皮层分层完全丧失。在RGCs中,需要Rap1 GTP酶来维持其极化组织。在新生神经元中,Rap1 GTP酶的缺失会阻止轴突和引导突起的形成,从而干扰径向迁移。综上所述,RGC和神经元极性的丧失导致皮层组织的破坏。