Kaluthantrige Don Flaminia, Kalebic Nereo
Human Technopole, Milan, Italy.
Front Cell Dev Biol. 2022 Jun 14;10:917166. doi: 10.3389/fcell.2022.917166. eCollection 2022.
The acquisition of higher intellectual abilities that distinguish humans from their closest relatives correlates greatly with the expansion of the cerebral cortex. This expansion is a consequence of an increase in neuronal cell production driven by the higher proliferative capacity of neural progenitor cells, in particular basal radial glia (bRG). Furthermore, when the proliferation of neural progenitor cells is impaired and the final neuronal output is altered, severe neurodevelopmental disorders can arise. To effectively study the cell biology of human bRG, genetically accessible human experimental models are needed. With the pioneering success to isolate and culture pluripotent stem cells , we can now routinely investigate the developing human cerebral cortex in a dish using three-dimensional multicellular structures called organoids. Here, we will review the molecular and cell biological features of bRG that have recently been elucidated using brain organoids. We will further focus on the application of this simple model system to study in a mechanistically actionable way the molecular and cellular events in bRG that can lead to the onset of various neurodevelopmental diseases.
人类所具备的、使其有别于近亲的更高智力能力的获得,与大脑皮层的扩张密切相关。这种扩张是神经祖细胞,特别是基底放射状胶质细胞(bRG)增殖能力增强所驱动的神经元细胞生成增加的结果。此外,当神经祖细胞的增殖受损且最终的神经元输出发生改变时,就可能出现严重的神经发育障碍。为了有效地研究人类bRG的细胞生物学,需要可进行基因操作的人类实验模型。随着分离和培养多能干细胞取得开创性成功,我们现在可以使用称为类器官的三维多细胞结构,在培养皿中常规地研究发育中的人类大脑皮层。在此,我们将综述最近利用脑类器官阐明的bRG的分子和细胞生物学特征。我们还将进一步聚焦于这个简单模型系统的应用,以一种具有机制可操作性的方式研究bRG中可能导致各种神经发育疾病发生的分子和细胞事件。