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Rapid generation of functional dopaminergic neurons from human induced pluripotent stem cells through a single-step procedure using cell lineage transcription factors

机译:使用细胞谱系转录因子通过一步法从人诱导的多能干细胞快速生成功能性多巴胺能神经元

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摘要

Current protocols for in vitro differentiation of human induced pluripotent stem cells (hiPSCs) to generate dopamine (DA) neurons are laborious and time-expensive. In order to accelerate the overall process, we have established a fast protocol by expressing the developmental transcription factors ASCL1, NURR1, and LMX1A. With this method, we were able to generate mature and functional dopaminergic neurons in as few as 21 days, skipping all the intermediate steps for inducting and selecting embryoid bodies and rosette-neural precursors. Strikingly, the resulting neuronal conversion process was very proficient, with an overall efficiency that was more than 93% of all the coinfected cells. hiPSC-derived DA neurons expressed all the critical molecular markers of the DA molecular machinery and exhibited sophisticated functional features including spontaneous electrical activity and dopamine release. This one-step protocol holds important implications for in vitro disease modeling and is particularly amenable for exploitation in high-throughput screening protocols.
机译:当前的体外诱导人类诱导多能干细胞(hiPSC)分化以产生多巴胺(DA)神经元的协议既费力又费时。为了加快整个过程,我们通过表达发育转录因子ASCL1,NURR1和LMX1A建立了快速协议。使用这种方法,我们能够在短短21天之内生成成熟且功能强大的多巴胺能神经元,而跳过了诱导和选择胚状体和玫瑰花状神经前体的所有中间步骤。令人惊讶的是,由此产生的神经元转换过程非常熟练,总效率超过所有共感染细胞的93%。 hiPSC衍生的DA神经元表达了DA分子机器的所有关键分子标记,并表现出复杂的功能特征,包括自发的电活动和多巴胺释放。这一单步操作方案对体外疾病建模具有重要意义,尤其适用于高通量筛选方案。

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