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Expansion of human midbrain floor plate progenitors from induced pluripotent stem cells increases dopaminergic neuron differentiation potential

机译:从诱导多能干细胞扩增人中脑底板祖细胞可增加多巴胺能神经元分化潜能

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摘要

Human induced pluripotent stem cells (hiPSCs) are invaluable to study developmental processes and disease mechanisms particularly in the brain. hiPSCs can be differentiated into mature and functional dopaminergic (DA) neurons. Having robust protocols for the generation of differentiated DA neurons from pluripotent cells is a prerequisite for the use of hiPSCs to study disease mechanisms, for drug discovery, and eventually for cell replacement therapy. Here, we describe a protocol for generating and expanding large numbers of homogeneous midbrain floor plate progenitors (mFPPs) that retain efficient DA neurogenic potential over multiple passages and can be cryobanked. We demonstrate that expanded mFPPs have increased DA neuron potential and differentiate more efficiently and rapidly than progenitors generated by standard protocols. In addition, this novel method results in increased numbers of DA neurons that in vitro show characteristic electrophysiological properties of nigrostriatal DA neurons, produce high levels of dopamine, and integrate into host mice when grafted in vivo. Thus, we describe a robust method for producing human mesencephalic DA neurons from hiPSCs.
机译:人类诱导的多能干细胞(hiPSC)对于研究发育过程和疾病机制(特别是在大脑中)非常有价值。 hiPSC可以分为成熟的和功能性的多巴胺能(DA)神经元。具有从多能细胞生成分化DA神经元的可靠方案是使用hiPSC研究疾病机制,药物发现并最终用于细胞替代治疗的前提条件。在这里,我们描述了用于生成和扩展大量均质中脑楼板祖细胞(mFPPs)的协议,这些协议在多个传代中均保留了有效的DA神经源性潜能,并且可以冻存。我们证明,扩展的mFPPs具有增加的DA神经元潜力,并且比标准协议生成的祖细胞更有效,更快地分化。另外,这种新方法导致增加的DA神经元数量,这些DA神经元在体外显示出黑纹状体DA神经元的特征性电生理特性,产生高水平的多巴胺,并在体内移植时整合到宿主小鼠中。因此,我们描述了一种从hiPSCs产生人中脑DA神经元的鲁棒方法。

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