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Functional imaging of neuron-astrocyte interactions in a compartmentalized microfluidic device.在分隔式微流控装置中对神经元-星形胶质细胞相互作用进行功能成像。
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2
Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1.脑类器官揭示精神分裂症中的早期皮质发育不良——计算解剖学和基因组学,FGFR1 的作用。
Transl Psychiatry. 2017 Nov 17;7(11):6. doi: 10.1038/s41398-017-0054-x.
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Efficient Generation of CA3 Neurons from Human Pluripotent Stem Cells Enables Modeling of Hippocampal Connectivity In Vitro.高效地从人多能干细胞生成 CA3 神经元可实现体外海马连接的建模。
Cell Stem Cell. 2018 May 3;22(5):684-697.e9. doi: 10.1016/j.stem.2018.04.009.
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Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders.精神疾病中兴奋性/抑制性平衡的抑制性控制。
F1000Res. 2018 Jan 8;7:23. doi: 10.12688/f1000research.12155.1. eCollection 2018.
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Epigenetics and cerebral organoids: promising directions in autism spectrum disorders.表观遗传学与大脑类器官:自闭症谱系障碍的研究新方向。
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Reconstituting Corticostriatal Network on-a-Chip Reveals the Contribution of the Presynaptic Compartment to Huntington's Disease.在片上重建皮质纹状体网络揭示了突触前区对亨廷顿病的贡献。
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10
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分区设备作为研究人类大脑网络动力学的工具。

Compartmentalized Devices as Tools for Investigation of Human Brain Network Dynamics.

机构信息

Child Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey.

Department of Biomedical Engineering, Rutgers University, Piscataway, New Jersey.

出版信息

Dev Dyn. 2019 Jan;248(1):65-77. doi: 10.1002/dvdy.24665. Epub 2018 Sep 12.

DOI:10.1002/dvdy.24665
PMID:30117633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6312734/
Abstract

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.

摘要

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