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Efficient Generation of Viral and Integration-Free Human Induced Pluripotent Stem Cell-Derived Oligodendrocytes

机译:有效地产生病毒和无铅人诱导多能干细胞衍生的少突胶质细胞

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摘要

Here we document three highly reproducible protocols: (1) a culture system for the derivation of human oligodendrocytes (OLs) from human induced pluripotent stem cells (hiPS) and their further maturation—our protocol generates viral- and integration-free OLs that efficiently commit and move forward in the OL lineage, recapitulating all the steps known to occur during in vivo development; (2) a method for the isolation, propagation and maintenance of neural stem cells (NSCs); and (3) a protocol for the production, isolation, and maintenance of OLs from perinatal rodent and human brain-derived NSCs. Our unique culture systems rely on a series of chemically defined media, specifically designed and carefully characterized for each developmental stage of OL as they advance from OL progenitors to mature, myelinating cells. We are confident that these protocols bring our field a step closer to efficient autologous cell replacement therapies and disease modeling.
机译:在这里,我们将三种高度可重复的协议记录:(1)从人诱导的多能干细胞(臀部)的人寡核细胞(OLS)衍生的培养系统及其进一步成熟 - 我们的协议产生有效提交的病毒和一体化的OLS 并在OL谱系中向前移动,重新承载在体内开发期间已知的所有步骤; (2)神经干细胞(NSCs)分离,传播和维持的方法; (3)来自围产期啮齿动物和人脑衍生的NSC的OLS的生产,分离和维持的方案。 我们独特的培养系统依赖于一系列化学定义的介质,专门设计和仔细描述于OL的每个发育阶段,因为它们从OL祖细胞进入成熟,髓鞘细胞。 我们相信这些协议带来了我们的领域更接近高效的自体细胞更换疗法和疾病建模的一步。

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