Child Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey.
Department of Biomedical Engineering, Rutgers University, Piscataway, New Jersey.
Dev Dyn. 2019 Jan;248(1):65-77. doi: 10.1002/dvdy.24665. Epub 2018 Sep 12.
Neuropsychiatric disorders have traditionally been difficult to study due to the complexity of the human brain and limited availability of human tissue. Induced pluripotent stem (iPS) cells provide a promising avenue to further our understanding of human disease mechanisms, but traditional 2D cell cultures can only provide a limited view of the neural circuits. To better model complex brain neurocircuitry, compartmentalized culturing systems and 3D organoids have been developed. Early compartmentalized devices demonstrated how neuronal cell bodies can be isolated both physically and chemically from neurites. Soft lithographic approaches have advanced this approach and offer the tools to construct novel model platforms, enabling circuit-level studies of disease, which can accelerate mechanistic studies and drug candidate screening. In this review, we describe some of the common technologies used to develop such systems and discuss how these lithographic techniques have been used to advance our understanding of neuropsychiatric disease. Finally, we address other in vitro model platforms such as 3D culture systems and organoids and compare these models with compartmentalized models. We ask important questions regarding how we can further harness iPS cells in these engineered culture systems for the development of improved in vitro models. Developmental Dynamics 248:65-77, 2019. © 2018 Wiley Periodicals, Inc.
神经精神疾病由于人脑的复杂性和人类组织的有限可用性,传统上一直难以研究。诱导多能干细胞(iPS)为进一步了解人类疾病机制提供了有希望的途径,但传统的 2D 细胞培养只能提供对神经回路的有限观察。为了更好地模拟复杂的大脑神经回路,已经开发了分区培养系统和 3D 类器官。早期的分区设备展示了如何在物理和化学上从神经突中分离神经元细胞体。软光刻方法推进了这一方法,并提供了构建新型模型平台的工具,从而能够进行疾病的回路级研究,从而加速机制研究和候选药物筛选。在这篇综述中,我们描述了一些用于开发此类系统的常用技术,并讨论了这些光刻技术如何用于加深我们对神经精神疾病的理解。最后,我们讨论了其他体外模型平台,如 3D 培养系统和类器官,并将这些模型与分区模型进行了比较。我们提出了一些重要的问题,即我们如何在这些工程化培养系统中进一步利用 iPS 细胞来开发改进的体外模型。发育动力学 248:65-77,2019。©2018 威利父子公司