将神经祖细胞的低密度传代与转录因子 NFIA 的转分化相结合,从人类诱导多能干细胞中生成 iAstrocytes。

Patrick Bosco, Ugur Akcan, Damian Williams, Heather M. Buchanan, Dritan Agalliu, Andrew A. Sproul
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引用次数: 0

摘要

星形胶质细胞是中枢神经系统(CNS)稳态的关键调节因子,其功能障碍与神经系统和神经退行性疾病有关。在这里,我们介绍了一种分两步从人类诱导多能干细胞(hiPSCs)中生成星形胶质细胞的方案,首先使用可保存的神经祖细胞(NPC)中间体,然后进行低密度传代,并过表达神经胶质转录因子NFIA。可储存的 NPC 中间体可根据实验需要,从同一遗传背景中同时分化出纯化的神经元和星形胶质细胞类型。本文介绍了一种从 hiPSC 生成 NPC 的方案,然后将其分化成源于 hiPSC 的星形胶质细胞(称为 iAstrocytes)。通过批量 RNA-Seq 和免疫细胞化学,产生的 iAstrocytes 在转录本和蛋白质水平上分别表达了星形胶质细胞特征的关键标志物。此外,iAstrocytes 还能对多聚(I:C)炎症刺激做出反应,并在体力活动或添加 ATP 的情况下产生钙活性波。我们的方法提供了一种生成和表征人类星形胶质细胞的简单而稳健的方法,可用于模拟影响这种细胞类型的人类疾病。© 2024 Wiley Periodicals LLC.基本方案 1:将 hiPSCs 分化为 NPCs 基本方案 2:将 NPCs 分化为 iAstrocytes 支持方案 1:iAstrocytes 的分子验证 支持方案 2:基于钙成像的 iAstrocyte 功能验证 支持方案 3:将 NPCs 分化为神经元。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generating iAstrocytes From Human Induced Pluripotent Stem Cells by Combining Low-Density Passaging of Neural Progenitor Cells and Transcription Factor NFIA Transdifferentiation

Astrocytes are key regulators of central nervous system (CNS) homeostasis, and their dysfunction is implicated in neurological and neurodegenerative disorders. Here, we describe a two-step protocol to generate astrocytes from human induced pluripotent stem cells (hiPSCs) using a bankable neural progenitor cell (NPC) intermediate, followed by low-density passaging and overexpression of the gliogenic transcription factor NFIA. A bankable NPC intermediate allows for facile differentiation into both purified neuronal and astrocyte cell types in parallel from the same genetic background, depending on the experimental needs. This article presents a protocol to generate NPCs from hiPSCs, which are then differentiated into hiPSC-derived astrocytes, termed iAstrocytes. The resulting iAstrocytes express key markers of astrocyte identity at transcript and protein levels by bulk RNA-Seq and immunocytochemistry, respectively. Additionally, they respond to the inflammatory stimuli poly(I:C) and generate waves of calcium activity in response to either physical activity or the addition of ATP. Our approach offers a simple and robust method to generate and characterize human astrocytes, which can be used to model human disease affecting this cell type. © 2024 Wiley Periodicals LLC.

Basic Protocol 1: Differentiation of hiPSCs to NPCs

Basic Protocol 2: Differentiation of NPCs into iAstrocytes

Support Protocol 1: Molecular validation of iAstrocytes

Support Protocol 2: Calcium imaging-based validation of iAstrocyte function

Support Protocol 3: Differentiation of NPCs into neurons

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