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Fast Generation of Functional Subtype Astrocytes from Human Pluripotent Stem Cells

  • Xiang Li
  • , Yezheng Tao
  • , Robert Bradley
  • , Zhongwei Du
  • , Yunlong Tao
  • , Linghai Kong
  • , Yi Dong
  • , Jeffrey Jones
  • , Yuanwei Yan
  • , Cole R.K. Harder
  • , Lindsay Morgan Friedman
  • , Magd Bilal
  • , Brianna Hoffmann
  • , Su Chun Zhang*
  • *此作品的通讯作者
  • University of Wisconsin-Madison
  • BrainXell
  • Department of Medicine and Neuroscience
  • Department of Neurology

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

Differentiation of astrocytes from human pluripotent stem cells (hPSCs) is a tedious and variable process. This hampers the study of hPSC-generated astrocytes in disease processes and drug development. By using CRISPR/Cas9-mediated inducible expression of NFIA or NFIA plus SOX9 in hPSCs, we developed a method to efficiently generate astrocytes in 4–7 weeks. The astrocytic identity of the induced cells was verified by their characteristic molecular and functional properties as well as after transplantation. Furthermore, we developed a strategy to generate region-specific astrocyte subtypes by combining differentiation of regional progenitors and transgenic induction of astrocytes. This simple and efficient method offers a new opportunity to study the fundamental biology of human astrocytes and their roles in disease processes. In this article, Zhang and colleagues show that functional and subtype-specific astrocytes can be fast generated from hPSCs by using CRISPR/Cas9-mediated inducible expression of NFIA or NFIA plus SOX9 in hPSCs. This simple and efficient method offers the opportunity to study the fundamental biology of human astrocytes and their roles in disease processes.

源语言英语
页(从-至)998-1008
页数11
期刊Stem Cell Reports
卷11
期4
DOI
出版状态已出版 - 9 10月 2018
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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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