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MicroRNA-based conversion of human fibroblasts into striatal medium spiny neurons

机译:基于MicroRNA的人类成纤维细胞向纹状体中棘神经元的转化

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The ability to generate human neurons of specific subtypes of clinical importance offers experimental platforms that may be instrumental for disease modeling. We recently published a study demonstrating the use of neuronal microRNAs (miRNAs) and transcription factors to directly convert human fibroblasts to a highly enriched population of striatal medium spiny neurons (MSNs), a neuronal subpopulation that has a crucial role in motor control and harbors selective susceptibility to cell death in Huntington's disease. Here we describe a stepwise protocol for the generation of MSNs by direct neuronal conversion of human fibroblasts in 30 d. We provide descriptions of cellular behaviors during reprogramming and crucial steps involved in gene delivery, cell adhesion and culturing conditions that promote cell survival. Our protocol offers a unique approach to combine microRNAs and transcription factors to guide the neuronal conversion of human fibroblasts toward a specific neuronal subtype.
机译:产生具有临床重要性的特定亚型的人类神经元的能力提供了可能对疾病建模有用的实验平台。我们最近发表了一项研究,证明了使用神经元microRNA(miRNA)和转录因子将人类成纤维细胞直接转化为高度富集的纹状体中棘神经元(MSN),这是一种神经元亚群,在运动控制中起着至关重要的作用,具有选择性亨廷顿氏病对细胞死亡的敏感性。在这里,我们描述了人类成纤维细胞在30天内通过直接神经元转换生成MSN的分步协议。我们提供了重编程过程中的细胞行为的描述,以及基因传递,细胞粘附和促进细胞存活的培养条件中涉及的关键步骤。我们的协议提供了一种结合microRNA和转录因子的独特方法,以指导人类成纤维细胞向特定神经元亚型的神经元转化。

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