van Voorst Torben W, van Boven Maaike A, Marinus Kevin I, Colón-Mercado Jennifer M, Schretzmeir Jule, Haag Carolin, Toonen Ruud F, Koopmans Frank, Ward Michael E, Smit August B, van Kesteren Ronald E, Verhage Matthijs, Cornelisse L Niels
Department of Functional Genomics, Center for Neurogenomics and Cognitive Research (CNCR), VU University Amsterdam, de Boelelaan 1100, 1081 HZ Amsterdam, The Netherlands.
Department of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research (CNCR), VU University Amsterdam, de Boelelaan 1100, 1081 HZ Amsterdam, The Netherlands.
bioRxiv. 2025 Jul 7:2025.06.30.662293. doi: 10.1101/2025.06.30.662293.
Human induced pluripotent stem cells (iPSCs) present a powerful approach to study human brain physiology and disease, yet robust, pure GABAergic induction has remained difficult. Here we present improved, single-step, transposon-based GABAergic induction with Ascl1/Dlx2, which yields pure GABAergic neurons, in contrast to lentiviral approaches, and was tested across three independent iPSC lines. Proteomic and electrophysiological characterization at different developmental time points showed that these neurons gain a proteomic profile that maps to different cortical interneuron subtypes, particularly VIP+ interneurons, and display typical GABAergic synaptic properties, producing large, synchronous and picrotoxin-sensitive currents. During early development synaptic strength increased threefold, which was accompanied by enhanced expression of multiple GABA-specific presynaptic gene sets, but few changes in postsynaptic gene sets. Synaptic strength continued to improve during late development but with only minor proteomic changes. Co-seeding with NGN2 neurons created stable networks of predefined excitation/inhibition ratios, with corresponding synapse ratios. Taken together, transposon-based GABAergic induction yields pure, mature GABAergic neurons suitable for studying gene sets involved in synaptic maturation and to build excitation/inhibition networks for disease modelling.
人类诱导多能干细胞(iPSC)为研究人类大脑生理学和疾病提供了一种强大的方法,但强大而纯净的γ-氨基丁酸能(GABAergic)诱导仍然具有挑战性。在此,我们展示了一种改进的、基于转座子的单步Ascl1/Dlx2介导的GABA能诱导方法,与慢病毒方法相比,该方法可产生纯净的GABA能神经元,并在三个独立的iPSC系中进行了测试。在不同发育时间点的蛋白质组学和电生理学特征表明,这些神经元获得了一种蛋白质组学特征,可映射到不同的皮质中间神经元亚型,特别是血管活性肠肽(VIP)阳性中间神经元,并表现出典型的GABA能突触特性,产生大的、同步的和对印防己毒素敏感的电流。在早期发育过程中,突触强度增加了三倍,同时多个GABA特异性突触前基因集的表达增强,但突触后基因集变化很少。在晚期发育过程中,突触强度持续改善,但蛋白质组学变化较小。与神经生成蛋白2(NGN2)神经元共接种可创建具有预定义兴奋/抑制比率和相应突触比率的稳定网络。综上所述,基于转座子的GABA能诱导可产生纯净、成熟的GABA能神经元,适用于研究参与突触成熟的基因集,并构建用于疾病建模的兴奋/抑制网络。