Cell Fate Engineering and Disease Modeling Group, German Cancer Research Center (DKFZ) and DKFZ-ZMBH Alliance, Heidelberg, Germany.
HITBR Hector Institute for Translational Brain Research gGmbH, Heidelberg, Germany.
Methods Mol Biol. 2021;2352:1-12. doi: 10.1007/978-1-0716-1601-7_1.
Forced expression of specific neuronal transcription factors in mouse embryonic fibroblasts (MEFs) can lead to their direct conversion into functional neurons. Direct neuronal reprogramming has become a powerful tool to characterize individual factors and molecular mechanisms involved in forced and normal neurogenesis and to generate neuronal cell types for in vitro studies. Here we provide a detailed protocol for the isolation of MEFs devoid of neural tissue and their direct reprogramming into functional neurons by overexpression of neuronal reprogramming factors (Ascl1, Brn2, and Myt1l) using lentiviral vectors. This method enables quick and efficient generation of mouse neurons in vitro for versatile functional and mechanistic characterization.
在小鼠胚胎成纤维细胞(MEFs)中强制表达特定的神经元转录因子可以直接将其转化为功能性神经元。直接神经元重编程已成为一种强大的工具,可以用于研究特定因子和分子机制在强制和正常神经发生中的作用,并生成用于体外研究的神经元细胞类型。在这里,我们提供了一个详细的方案,用于分离没有神经组织的 MEFs,并通过慢病毒载体过表达神经元重编程因子(Ascl1、Brn2 和 Myt1l)将其直接重编程为功能性神经元。这种方法可快速有效地在体外生成小鼠神经元,用于多功能的功能和机制表征。