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本文引用的文献

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Studying Human Neurodevelopment and Diseases Using 3D Brain Organoids.使用 3D 脑类器官研究人类神经发育和疾病。
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Synergistic effects of common schizophrenia risk variants.常见精神分裂症风险变异的协同效应。
Nat Genet. 2019 Oct;51(10):1475-1485. doi: 10.1038/s41588-019-0497-5. Epub 2019 Sep 23.
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CRISPR Interference-Based Platform for Multimodal Genetic Screens in Human iPSC-Derived Neurons.基于 CRISPR 干扰的平台,用于在人类 iPSC 衍生神经元中进行多模式遗传筛选。
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Individual brain organoids reproducibly form cell diversity of the human cerebral cortex.个体脑类器官可重现形成人类大脑皮层的细胞多样性。
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An Autaptic Culture System for Standardized Analyses of iPSC-Derived Human Neurons.一种用于 iPSC 衍生的人类神经元标准化分析的自突培养系统。
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A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons.人诱导多能干细胞源性神经元的突触传递和可塑性的单细胞模型。
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SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neurons.SHANK2 基因突变与自闭症谱系障碍有关,导致人类神经元过度连接。
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Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders.定义精神疾病的遗传、基因组、细胞和诊断结构。
Cell. 2019 Mar 21;177(1):162-183. doi: 10.1016/j.cell.2019.01.015.
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Human pluripotent stem cell-derived models and drug screening in CNS precision medicine.人多能干细胞衍生模型与中枢神经系统精准医学中的药物筛选。
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hESC-Derived Thalamic Organoids Form Reciprocal Projections When Fused with Cortical Organoids.人胚胎干细胞衍生的丘脑类器官与皮质类器官融合后形成相互投射。
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整合 CRISPR 工程和 hiPSC 衍生的 2D 疾病建模系统。

Integrating CRISPR Engineering and hiPSC-Derived 2D Disease Modeling Systems.

机构信息

Department of Genetics and Genomics.

Friedman Brain Institute.

出版信息

J Neurosci. 2020 Feb 5;40(6):1176-1185. doi: 10.1523/JNEUROSCI.0518-19.2019.

DOI:10.1523/JNEUROSCI.0518-19.2019
PMID:32024766
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7002154/
Abstract

Human induced pluripotent stem cells (hiPSCs) have revolutionized research on human diseases, particularly neurodegenerative and psychiatric disorders, making it possible to study mechanisms of disease risk and initiation in otherwise inaccessible patient-specific cells. Today, the integration of CRISPR engineering approaches with hiPSC-based models permits precise isogenic comparisons of human neurons and glia. This review is intended as a guideline for neuroscientists and clinicians interested in translating their research to hiPSC-based studies. It offers state-of-the-art approaches to tackling the challenges that are unique to human disease models, particularly interdonor and intradonor variability, and limitations in neuronal maturity and circuit complexity. Finally, we provide a detailed overview of the immense possibilities the field has to offer, highlighting efficient neural differentiation and induction strategies for the major brain cell types and providing perspective into integrating CRISPR-based methods into study design. The combination of hiPSC-based disease modeling, CRISPR technology, and high-throughput approaches promises to advance our scientific knowledge and accelerate progress in drug discovery. Studying Human Neurodevelopment and Diseases Using 3D Brain Organoids, by Ai Tian, Julien Muffat, and Yun Li.

摘要

人类诱导多能干细胞(hiPSCs)彻底改变了人类疾病的研究,特别是神经退行性和精神疾病的研究,使得研究疾病风险和发病机制成为可能,而这些研究在原本无法接触的患者特异性细胞中是不可能进行的。如今,CRISPR 工程方法与基于 hiPSC 的模型的结合,使得对人类神经元和神经胶质细胞进行精确同基因比较成为可能。这篇综述旨在为对将其研究转化为基于 hiPSC 的研究感兴趣的神经科学家和临床医生提供指导。它提供了最新的方法来解决人类疾病模型所特有的挑战,特别是供体间和供体内变异性,以及神经元成熟度和回路复杂性的限制。最后,我们详细介绍了该领域提供的巨大可能性,重点介绍了主要脑细胞类型的高效神经分化和诱导策略,并探讨了将基于 CRISPR 的方法整合到研究设计中的问题。基于 hiPSC 的疾病建模、CRISPR 技术和高通量方法的结合有望推进我们的科学知识,并加速药物发现的进展。《利用 3D 脑类器官研究人类神经发育和疾病》,作者 Ai Tian、Julien Muffat 和 Yun Li。