Peyre Elise, Silva Carla G, Nguyen Laurent
GIGA-Neurosciences, University of Liège Liège, Belgium ; Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège Liège, Belgium.
GIGA-Neurosciences, University of Liège Liège, Belgium ; Interdisciplinary Cluster for Applied Genoproteomics (GIGA-R), University of Liège Liège, Belgium ; Wallon Excellence in Lifesciences and Biotechnology, University of Liège Liège, Belgium.
Front Cell Neurosci. 2015 Apr 14;9:129. doi: 10.3389/fncel.2015.00129. eCollection 2015.
During embryogenesis, cortical interneurons are generated by ventral progenitors located in the ganglionic eminences of the telencephalon. They travel along multiple tangential paths to populate the cortical wall. As they reach this structure they undergo intracortical dispersion to settle in their final destination. At the cellular level, migrating interneurons are highly polarized cells that extend and retract processes using dynamic remodeling of microtubule and actin cytoskeleton. Different levels of molecular regulation contribute to interneuron migration. These include: (1) Extrinsic guidance cues distributed along migratory streams that are sensed and integrated by migrating interneurons; (2) Intrinsic genetic programs driven by specific transcription factors that grant specification and set the timing of migration for different subtypes of interneurons; (3) Adhesion molecules and cytoskeletal elements/regulators that transduce molecular signalings into coherent movement. These levels of molecular regulation must be properly integrated by interneurons to allow their migration in the cortex. The aim of this review is to summarize our current knowledge of the interplay between microenvironmental signals and cell autonomous programs that drive cortical interneuron porduction, tangential migration, and intergration in the developing cerebral cortex.
在胚胎发育过程中,皮质中间神经元由位于端脑神经节隆起处的腹侧祖细胞产生。它们沿着多条切线路径迁移,以填充皮质壁。当它们到达这个结构时,会在皮质内扩散,以定居在它们的最终目的地。在细胞水平上,迁移中的中间神经元是高度极化的细胞,它们通过微管和肌动蛋白细胞骨架的动态重塑来伸展和收缩突起。不同水平的分子调控有助于中间神经元的迁移。这些包括:(1) 沿着迁移流分布的外在引导信号,迁移中的中间神经元可感知并整合这些信号;(2) 由特定转录因子驱动的内在遗传程序,这些转录因子赋予中间神经元不同亚型特异性并设定其迁移时间;(3) 黏附分子以及将分子信号转化为连贯运动的细胞骨架元件/调节剂。中间神经元必须正确整合这些分子调控水平,才能在皮质中迁移。本综述的目的是总结我们目前对微环境信号与细胞自主程序之间相互作用的认识,这些相互作用驱动着发育中的大脑皮质中皮质中间神经元的产生、切线迁移和整合。