Efficient generation of functional neurons from mouse embryonic stem cells via Neurogenin-2 expression

The production of induced neuronal (iN) cells from human embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) by the forced expression of proneural transcription factors is rapid, efficient, and reproducible. The ability to generate large numbers of human neurons in such a robust manner enables large-scale studies of human neural differentiation and neuropsychiatric diseases. Surprisingly, similar transcription factor-based approaches for converting mouse ESCs into iN cells have been challenging, primarily due to low cell survival. Here, we provide a detailed approach for the efficient and reproducible generation of functional iN cells from mouse ESCs cultures by the genetically induced expression of Neurogenin-2. The resulting iN cells display mature pre- and postsynaptic specializations and form synaptic networks. Our method provides the basis for studying neuronal development and enables the direct comparison of cellular phenotypes in mouse and human neurons generated in an equivalent way. The procedure requires 14 days and can be carried out by users with expertise in stem cell culture.