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用于体外研究脑疾病的患者特异性神经细胞的构建。

Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders.

机构信息

Department of Psychiatry, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY 10029, USA.

Laboratory of Genetics, Salk Institute for Biological Studies, 10010 North Torrey Pines Road, San Diego, CA 92037, USA.

出版信息

Stem Cell Reports. 2015 Dec 8;5(6):933-945. doi: 10.1016/j.stemcr.2015.10.011. Epub 2015 Nov 21.

DOI:10.1016/j.stemcr.2015.10.011
PMID:26610635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4881284/
Abstract

As a group, we met to discuss the current challenges for creating meaningful patient-specific in vitro models to study brain disorders. Although the convergence of findings between laboratories and patient cohorts provided us confidence and optimism that hiPSC-based platforms will inform future drug discovery efforts, a number of critical technical challenges remain. This opinion piece outlines our collective views on the current state of hiPSC-based disease modeling and discusses what we see to be the critical objectives that must be addressed collectively as a field.

摘要

我们聚集在一起讨论了目前在创建有意义的用于研究脑疾病的患者特异性体外模型方面所面临的挑战。虽然实验室和患者队列的研究结果趋同,使我们有信心和乐观地认为基于 hiPSC 的平台将为未来的药物发现工作提供信息,但仍存在许多关键技术挑战。本文概述了我们对基于 hiPSC 的疾病建模现状的集体看法,并讨论了我们认为作为一个领域必须共同解决的关键目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/4881284/fbb5411536b4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/4881284/f899f32d3222/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/4881284/fbb5411536b4/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/4881284/f899f32d3222/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/4881284/fbb5411536b4/gr2.jpg

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2
Pluripotent stem cell-derived radial glia-like cells as stable intermediate for efficient generation of human oligodendrocytes.多能干细胞衍生的放射状胶质样细胞作为高效生成人少突胶质细胞的稳定中间体。
Glia. 2015 Dec;63(12):2152-67. doi: 10.1002/glia.22882. Epub 2015 Jun 30.
3
An alternative pluripotent state confers interspecies chimaeric competency.
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Epigenomics. 2021 Nov;13(21):1747-1759. doi: 10.2217/epi-2020-0136. Epub 2021 Mar 22.
4
Integration of Human Induced Pluripotent Stem Cell (hiPSC)-Derived Neurons into Rat Brain Circuits.人诱导多能干细胞(hiPSC)衍生的神经元融入大鼠脑回路
Bio Protoc. 2020 Sep 5;10(17):e3746. doi: 10.21769/BioProtoc.3746.
5
Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells.在源自患者的脑细胞中揭示帕金森病的遗传易感性。
NPJ Parkinsons Dis. 2020 Apr 24;6:8. doi: 10.1038/s41531-020-0110-8. eCollection 2020.
6
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Cell Rep. 2019 Dec 24;29(13):4646-4656.e4. doi: 10.1016/j.celrep.2019.11.111.
7
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8
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4
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5
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