Arai Yoko, Taverna Elena
Centre for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS UMR 7241/INSERM U1050, PSL Research University, Paris, France.
Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology (MPG), Leipzig, Germany.
Front Cell Neurosci. 2017 Dec 5;11:384. doi: 10.3389/fncel.2017.00384. eCollection 2017.
Neurons populating the cerebral cortex are generated during embryonic development from neural stem and progenitor cells in a process called neurogenesis. Neural stem and progenitor cells are classified into several classes based on the different location of mitosis (apical or basal) and polarity features (bipolar, monopolar and non-polar). The polarized architecture of stem cells is linked to the asymmetric localization of proteins, mRNAs and organelles, such as the centrosome and the Golgi apparatus (GA). Polarity affects stem cell function and allows stem cells to integrate environmental cues from distinct niches in the developing cerebral cortex. The crucial role of polarity in neural stem and progenitor cells is highlighted by the fact that impairment of cell polarity is linked to neurodevelopmental disorders such as Down syndrome, Fragile X syndrome, autism spectrum disorders (ASD) and schizophrenia.
在胚胎发育过程中,通过一个称为神经发生的过程,神经干细胞和祖细胞产生了构成大脑皮层的神经元。神经干细胞和祖细胞根据有丝分裂的不同位置(顶端或基底)和极性特征(双极、单极和非极性)被分为几类。干细胞的极性结构与蛋白质、mRNA和细胞器(如中心体和高尔基体)的不对称定位有关。极性影响干细胞功能,并使干细胞能够整合来自发育中的大脑皮层不同微环境的环境信号。细胞极性受损与唐氏综合征、脆性X综合征、自闭症谱系障碍(ASD)和精神分裂症等神经发育障碍有关,这一事实凸显了极性在神经干细胞和祖细胞中的关键作用。