Costa Marcos R, Müller Ulrich
Brain Institute, Federal University of Rio Grande do Norte Natal, Brazil.
Dorris Neuroscience Center and Department of Cell Biology, The Scripps Research Institute La Jolla, CA, USA.
Front Cell Neurosci. 2015 Jan 12;8:449. doi: 10.3389/fncel.2014.00449. eCollection 2014.
The mature cerebral cortex harbors a heterogeneous population of glutamatergic neurons, organized into a highly intricate histological architecture. Classically, this mixed population of neurons was thought to be generated sequentially from a seemingly homogenous group of progenitors under the influence of external cues. This view, however, has been challenged in the last decade by evidences pointing to the existence of fate-restricted neuronal progenitors in the developing neocortex. Here, we review classical studies using cell transplantation, retroviral labeling and cell culture, as well as new data from genetic fate-mapping analysis, to discuss the lineage relationships between neocortical progenitors and subclasses of excitatory neurons. We also propose a temporal model to conciliate the existence of fate-restricted progenitors alongside multipotent progenitors in the neocortex. Finally, we discuss evidences for a critical period of plasticity among post mitotic excitatory cortical neurons when environmental influences could change neuronal cell fate.
成熟的大脑皮层含有多种谷氨酸能神经元,它们组织成高度复杂的组织学结构。传统上,人们认为这种混合的神经元群体是在外部信号的影响下,从看似同质的祖细胞群体中依次产生的。然而,在过去十年中,这一观点受到了挑战,有证据表明在发育中的新皮层中存在命运受限的神经元祖细胞。在这里,我们回顾了使用细胞移植、逆转录病毒标记和细胞培养的经典研究,以及基因命运图谱分析的新数据,以讨论新皮层祖细胞与兴奋性神经元亚类之间的谱系关系。我们还提出了一个时间模型,以协调新皮层中命运受限祖细胞与多能祖细胞的共存。最后,我们讨论了有丝分裂后兴奋性皮层神经元可塑性关键期的证据,此时环境影响可能会改变神经元细胞命运。