Vajaria Ruby, Davis DeAsia, Tamagnini Francesco, McMillan Duncan G G, Vasudevan Nandini, Delivopoulos Evangelos
School of Biological Sciences, University of Reading, Reading RG6 6UB, UK.
School of Pharmacy, University of Reading, Reading RG6 6UR, UK.
Int J Mol Sci. 2025 Aug 28;26(17):8372. doi: 10.3390/ijms26178372.
Multiple differentiation protocols have emerged in recent years, producing neurons with diverse morphologies, gene and protein expression profiles, and functionality. Many of these differentiation techniques require months of culture and the use of expensive growth factors. Most importantly, the derived neurons usually do not exhibit any electrical activity. This limits the value of the protocol as a tool for engineering and investigating neural networks. Here, we describe an efficacious method for differentiating mouse embryonic stem cells into functional neurons. CGR8 cells were neurally induced via the simultaneous application of retinoic acid and purmorphamine. The derived cells expressed neuronal (TUJ1 and NeuN) and synaptic (GAD2, PSD-95, Synaptophysin, and VGLUT1) markers. During whole-cell recordings, neurons exhibited inward and outward currents, likely caused by fast-inactivating voltage-gated potassium channels. Upon current injection, miniature action potentials were also recorded. The efficient generation of diverse subtypes of functional neurons can be a useful tool in fundamental investigations of neural network activity and translational studies.
近年来出现了多种分化方案,可产生具有不同形态、基因和蛋白质表达谱以及功能的神经元。这些分化技术中的许多都需要数月的培养以及使用昂贵的生长因子。最重要的是,所衍生的神经元通常不表现出任何电活动。这限制了该方案作为工程和研究神经网络工具的价值。在此,我们描述了一种将小鼠胚胎干细胞分化为功能性神经元的有效方法。通过同时应用视黄酸和嘌呤吗啡对CGR8细胞进行神经诱导。所衍生的细胞表达神经元标志物(TUJ1和NeuN)和突触标志物(GAD2、PSD - 95、突触素和VGLUT1)。在全细胞记录期间,神经元表现出内向和外向电流,这可能是由快速失活的电压门控钾通道引起的。在注入电流时,还记录到了微小动作电位。高效生成多种功能性神经元亚型可成为神经网络活动基础研究和转化研究中的有用工具。