Morphological and functional aspects of progenitors perturbed in cortical malformations

被引:41
作者
Bizzotto, Sara [1 ,2 ,3 ]
Francis, Fiona [1 ,2 ,3 ]
机构
[1] INSERM, UMRS 839, F-75005 Paris, France
[2] Univ Paris 06, Sorbonne Univ, Paris, France
[3] Inst Fer Moulin, Paris, France
关键词
neurodevelopment; mouse mutant; radial glial cells; proliferation; epilepsy; intellectual disability; lamination; INTERKINETIC NUCLEAR MIGRATION; CONGENITAL MUSCULAR-DYSTROPHY; ASYMMETRIC CELL DIVISIONS; MAMMALIAN CEREBRAL-CORTEX; OUTER SUBVENTRICULAR ZONE; WALKER-WARBURG-SYNDROME; PIAL BASEMENT-MEMBRANE; RECEPTOR-LIGAND PAIR; SPINDLE ORIENTATION; MITOTIC SPINDLE;
D O I
10.3389/fncel.2015.00030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In this review, we discuss molecular and cellular mechanisms important for the function of neuronal progenitors during development, revealed by their perturbation in different cortical malformations. We focus on a class of neuronal progenitors, radial glial cells (RGCs), which are renowned for their unique morphological and behavioral characteristics, constituting a key element during the development of the mammalian cerebral cortex. We describe how the particular morphology of these cells is related to their roles in the orchestration of cortical development and their influence on other progenitor types and post-mitotic neurons. Important for disease mechanisms, we overview what is currently known about RGC cellular components, cytoskeletal mechanisms, signaling pathways and cell cycle characteristics, focusing on how defects lead to abnormal development and cortical malformation phenotypes. The multiple recent entry points from human genetics and animal models are contributing to our understanding of this important cell type. Combining data from phenotypes in the mouse reveals molecules which potentially act in common pathways. Going beyond this, we discuss future directions that may provide new data in this expanding area.
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页数:25
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