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使用 3D 脑类器官研究人类神经发育和疾病。

Studying Human Neurodevelopment and Diseases Using 3D Brain Organoids.

机构信息

Program in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada.

Program in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, Ontario M5G 0A4, Canada,

出版信息

J Neurosci. 2020 Feb 5;40(6):1186-1193. doi: 10.1523/JNEUROSCI.0519-19.2019.

DOI:10.1523/JNEUROSCI.0519-19.2019
PMID:32024767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7002141/
Abstract

differentiation of pluripotent stem cells provides a systematic platform to study development and disease. Recent advances in brain organoid technology have created new opportunities to investigate the formation and function of the human brain, under physiological and pathological conditions. Brain organoids can be generated to model the cellular and structural development of the human brain, and allow the investigation of the intricate interactions between resident neural and glial cell types. Combined with new advances in gene editing, imaging, and genomic analysis, brain organoid technology can be applied to address questions pertinent to human brain development, disease, and evolution. However, the current iterations of brain organoids also have limitations in faithfully recapitulating the processes. In this perspective, we evaluate the recent progress in brain organoid technology, and discuss the experimental considerations for its utilization. Integrating CRISPR Engineering and hiPSC-Derived 2D Disease Modeling Systems, by Kristina Rehbach, Michael B. Fernando, and Kristen J. Brennand.

摘要

多能干细胞的分化为研究发育和疾病提供了一个系统的平台。最近,脑类器官技术的进步为在生理和病理条件下研究人脑的形成和功能创造了新的机会。脑类器官可以用来模拟人脑的细胞和结构发育,并允许研究驻留的神经和神经胶质细胞类型之间的复杂相互作用。结合基因编辑、成像和基因组分析方面的新进展,脑类器官技术可用于解决与人类大脑发育、疾病和进化相关的问题。然而,目前的脑类器官在忠实再现这些过程方面也存在局限性。在这篇观点文章中,我们评估了脑类器官技术的最新进展,并讨论了其应用的实验注意事项。整合 CRISPR 工程和 hiPSC 衍生的 2D 疾病建模系统,作者:Kristina Rehbach、Michael B. Fernando 和 Kristen J. Brennand。

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本文引用的文献

1
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。
Nature. 2019 Jun;570(7762):523-527. doi: 10.1038/s41586-019-1289-x. Epub 2019 Jun 5.
2
Genome-wide CRISPR screen for Zika virus resistance in human neural cells.全基因组 CRISPR 筛选人类神经细胞对寨卡病毒的抗性。
Proc Natl Acad Sci U S A. 2019 May 7;116(19):9527-9532. doi: 10.1073/pnas.1900867116. Epub 2019 Apr 24.
3
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation.双等位基因突变导致骨硬化性骨发育不良-假性骨营养不良疾病谱和伴有脑畸形的退行性脑病。
Am J Hum Genet. 2019 May 2;104(5):925-935. doi: 10.1016/j.ajhg.2019.03.004. Epub 2019 Apr 11.
4
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of Microglia.CSF1R 纯合突变可导致儿童起病的脑白质病,并可导致先天性小神经胶质细胞缺失。
Am J Hum Genet. 2019 May 2;104(5):936-947. doi: 10.1016/j.ajhg.2019.03.010. Epub 2019 Apr 11.
5
Specification of positional identity in forebrain organoids.前脑类器官中位置身份的规范。
Nat Biotechnol. 2019 Apr;37(4):436-444. doi: 10.1038/s41587-019-0085-3. Epub 2019 Apr 1.
6
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Cell Rep. 2019 Mar 19;26(12):3203-3211.e5. doi: 10.1016/j.celrep.2019.02.063.
7
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Nat Neurosci. 2019 Apr;22(4):669-679. doi: 10.1038/s41593-019-0350-2. Epub 2019 Mar 18.
8
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9
NFIA is a gliogenic switch enabling rapid derivation of functional human astrocytes from pluripotent stem cells.NFIA 是一种神经胶质发生开关,能够使多能干细胞快速分化为功能性人星形胶质细胞。
Nat Biotechnol. 2019 Mar;37(3):267-275. doi: 10.1038/s41587-019-0035-0. Epub 2019 Feb 25.
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Cell Stem Cell. 2019 Mar 7;24(3):487-497.e7. doi: 10.1016/j.stem.2018.12.015. Epub 2019 Feb 21.