评估Shiverer小鼠离体脑切片培养中人类ipsc衍生的少突胶质细胞髓鞘形成的方案。

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-03-21 Epub Date: 2025-01-30 DOI:10.1016/j.xpro.2025.103609
Themistoklis M Tsarouchas, Lida Zoupi, Anna Williams, Erin M Gibson
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引用次数: 0

摘要

人诱导多能干细胞(iPSC)衍生的少突胶质细胞是研究神经退行性和神经发育障碍异常髓鞘形成的有力工具;然而,它们在体外常常不能形成髓鞘。在这里,我们提出了一种使用离体模型进行轴突嵌套和节周分割的方案。我们描述了制备Shiverer小鼠脑切片培养,少突胶质细胞移植,可视化和分析的步骤。这种方法适合多种培养形式,突出了以成本和时间有效的方式筛选髓磷脂调节药物和化合物的潜力,同时减少了动物使用。
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Protocol for assessing myelination by human iPSC-derived oligodendrocytes in Shiverer mouse ex vivo brain slice cultures.

Human induced pluripotent stem cell (iPSC)-derived oligodendrocytes are a powerful tool for studying aberrant myelination in neurodegenerative and neurodevelopmental disorders; however, they often fail to myelinate in vitro. Here, we present a protocol for axonal ensheathment and perinodal segmentation using an ex vivo model. We describe steps for preparing Shiverer mouse brain slice cultures, oligodendrocyte transplantation, visualization, and analysis. This approach suits multiple culture formats, highlighting the potential for the screening of myelin-modulating drugs and compounds in a cost- and time-effective manner, while reducing animal use.

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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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