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Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids

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 dopamine...

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Autores principales: Smits, Lisa M., Magni, Stefano, Kinugawa, Kaoru, Grzyb, Kamil, Luginbühl, Joachim, Sabate-Soler, Sonia, Bolognin, Silvia, Shin, Jay W., Mori, Eiichiro, Skupin, Alexander, Schwamborn, Jens C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683480/
https://www.ncbi.nlm.nih.gov/pubmed/32737576
http://dx.doi.org/10.1007/s00441-020-03249-y
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author Smits, Lisa M.
Magni, Stefano
Kinugawa, Kaoru
Grzyb, Kamil
Luginbühl, Joachim
Sabate-Soler, Sonia
Bolognin, Silvia
Shin, Jay W.
Mori, Eiichiro
Skupin, Alexander
Schwamborn, Jens C.
author_facet Smits, Lisa M.
Magni, Stefano
Kinugawa, Kaoru
Grzyb, Kamil
Luginbühl, Joachim
Sabate-Soler, Sonia
Bolognin, Silvia
Shin, Jay W.
Mori, Eiichiro
Skupin, Alexander
Schwamborn, Jens C.
author_sort Smits, Lisa M.
collection PubMed
description 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00441-020-03249-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-76834802020-11-30 Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids Smits, Lisa M. Magni, Stefano Kinugawa, Kaoru Grzyb, Kamil Luginbühl, Joachim Sabate-Soler, Sonia Bolognin, Silvia Shin, Jay W. Mori, Eiichiro Skupin, Alexander Schwamborn, Jens C. Cell Tissue Res Regular Article 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00441-020-03249-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-07-31 2020 /pmc/articles/PMC7683480/ /pubmed/32737576 http://dx.doi.org/10.1007/s00441-020-03249-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Smits, Lisa M.
Magni, Stefano
Kinugawa, Kaoru
Grzyb, Kamil
Luginbühl, Joachim
Sabate-Soler, Sonia
Bolognin, Silvia
Shin, Jay W.
Mori, Eiichiro
Skupin, Alexander
Schwamborn, Jens C.
Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title_full Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title_fullStr Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title_full_unstemmed Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title_short Single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
title_sort single-cell transcriptomics reveals multiple neuronal cell types in human midbrain-specific organoids
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683480/
https://www.ncbi.nlm.nih.gov/pubmed/32737576
http://dx.doi.org/10.1007/s00441-020-03249-y
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