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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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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. |
format | Online Article Text |
id | pubmed-7683480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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