Luxembourg Centre for Systems Biomedicine (LCSB), Developmental and Cellular Biology, University of Luxembourg, Belvaux, Luxembourg.
Department of Future Basic Medicine, Nara Medical University, Kashihara, Nara, Japan.
Cell Tissue Res. 2020 Dec;382(3):463-476. doi: 10.1007/s00441-020-03249-y. Epub 2020 Jul 31.
Human stem cell-derived organoids have great potential for modelling physiological and pathological processes. They recapitulate in vitro the organization and function of a respective organ or part of an organ. Human midbrain organoids (hMOs) have been described to contain midbrain-specific dopaminergic neurons that release the neurotransmitter dopamine. However, the human midbrain contains also additional neuronal cell types, which are functionally interacting with each other. Here, we analysed hMOs at high-resolution by means of single-cell RNA sequencing (scRNA-seq), imaging and electrophysiology to unravel cell heterogeneity. Our findings demonstrate that hMOs show essential neuronal functional properties as spontaneous electrophysiological activity of different neuronal subtypes, including dopaminergic, GABAergic, glutamatergic and serotonergic neurons. Recapitulating these in vivo features makes hMOs an excellent tool for in vitro disease phenotyping and drug discovery.
人类干细胞衍生的类器官在模拟生理和病理过程方面具有巨大的潜力。它们在体外重现了相应器官或器官部分的组织和功能。已经描述了人类中脑类器官 (hMO) 包含中脑特异性多巴胺能神经元,这些神经元释放神经递质多巴胺。然而,人类中脑还包含其他具有相互功能作用的神经元细胞类型。在这里,我们通过单细胞 RNA 测序 (scRNA-seq)、成像和电生理学以高分辨率分析 hMO,以揭示细胞异质性。我们的研究结果表明,hMO 显示出不同神经元亚型(包括多巴胺能、GABA 能、谷氨酸能和 5-羟色胺能神经元)的自发性电生理活动等基本神经元功能特性。重现这些体内特征使 hMO 成为体外疾病表型和药物发现的优秀工具。