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Reproducible generation of human midbrain organoids for in vitro modeling of Parkinson’s disease

机译:用于帕金森病的体外建模的人中脑体内的可重复生成

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The study of human midbrain development and midbrain related diseases, like Parkinson’s disease (PD), is limited by deficiencies in the currently available and validated laboratory models. Three dimensional midbrain organoids represent an innovative strategy to recapitulate some aspects of the complexity and physiology of the human midbrain. Nevertheless, also these novel organoid models exhibit some inherent weaknesses, including the presence of a necrotic core and batch-to-batch variability. Here we describe an optimized approach for the standardized generation of midbrain organoids that addresses these limitations, while maintaining key features of midbrain development like dopaminergic neuron and astrocyte differentiation. Moreover, we have established a novel time-efficient, fit for purpose analysis pipeline and provided proof of concept for its usage by investigating toxin induced PD.
机译:人类中脑发展和中脑相关疾病的研究如帕金森病(PD),受当前可用和经过验证的实验室模型的缺陷受限。三维中脑器有机体代表着一种创新的策略,以概括人类中脑复杂性和生理学的一些方面。然而,这些新颖的有机体模型也表现出一些固有的弱点,包括存在坏死核和分批变异性。在这里,我们描述了解决这些限制的标准化的中脑有机体的标准化的优化方法,同时保持中脑开发的关键特征,如多巴胺能神经元和星形胶质细胞分化。此外,我们已经建立了一种新的延时,适合目的分析管道,并通过研究毒素诱导的Pd来提供概念证明。

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