Gurdon Institute, University of Cambridge, Cambridge, UK.
Nat Neurosci. 2012 Feb 5;15(3):477-86, S1. doi: 10.1038/nn.3041.
Efforts to study the development and function of the human cerebral cortex in health and disease have been limited by the availability of model systems. Extrapolating from our understanding of rodent cortical development, we have developed a robust, multistep process for human cortical development from pluripotent stem cells: directed differentiation of human embryonic stem (ES) and induced pluripotent stem (iPS) cells to cortical stem and progenitor cells, followed by an extended period of cortical neurogenesis, neuronal terminal differentiation to acquire mature electrophysiological properties, and functional excitatory synaptic network formation. We found that induction of cortical neuroepithelial stem cells from human ES cells and human iPS cells was dependent on retinoid signaling. Furthermore, human ES cell and iPS cell differentiation to cerebral cortex recapitulated in vivo development to generate all classes of cortical projection neurons in a fixed temporal order. This system enables functional studies of human cerebral cortex development and the generation of individual-specific cortical networks ex vivo for disease modeling and therapeutic purposes.
在健康和疾病状态下研究人类大脑皮层的发育和功能的努力受到模型系统可用性的限制。我们根据对啮齿动物皮层发育的理解,开发了一种从多能干细胞产生人类皮层发育的强大、多步骤的过程:定向分化人类胚胎干细胞(ES)和诱导多能干细胞(iPS)细胞为皮层干细胞和祖细胞,随后是延长的皮层神经发生、神经元终末分化以获得成熟的电生理特性和功能兴奋性突触网络形成。我们发现,诱导人类 ES 细胞和人类 iPS 细胞的皮层神经上皮干细胞依赖于视黄酸信号。此外,人类 ES 细胞和 iPS 细胞向大脑皮层的分化再现了体内发育,以固定的时间顺序产生所有类别的皮层投射神经元。该系统能够对人类大脑皮层发育进行功能研究,并在体外生成个体特异性皮层网络,用于疾病建模和治疗目的。