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A facile method to generate cerebral organoids from human pluripotent stem cells
Human cerebral organoids (COs) are self-organizing three-dimensional (3D) neural structures that provide a human-specific platform to study the cellular and molecular processes that underlie different neurological events. The first step of CO generation from human pluripotent stem cells (hPSCs) is n...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Leibniz Research Centre for Working Environment and Human Factors
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620858/ https://www.ncbi.nlm.nih.gov/pubmed/37927348 http://dx.doi.org/10.17179/excli2023-6299 |
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author | Simorgh, Susan Mousavi, Seyed Ahmad To, San Kit Pasque, Vincent Wierda, Keimpe Vervliet, Tim Yeganeh, Meghdad Pooyan, Paria Chai, Yoke Chin Verfaillie, Catherine Baharvand, Hossein |
author_facet | Simorgh, Susan Mousavi, Seyed Ahmad To, San Kit Pasque, Vincent Wierda, Keimpe Vervliet, Tim Yeganeh, Meghdad Pooyan, Paria Chai, Yoke Chin Verfaillie, Catherine Baharvand, Hossein |
author_sort | Simorgh, Susan |
collection | PubMed |
description | Human cerebral organoids (COs) are self-organizing three-dimensional (3D) neural structures that provide a human-specific platform to study the cellular and molecular processes that underlie different neurological events. The first step of CO generation from human pluripotent stem cells (hPSCs) is neural induction, which is an in vitro simulation of neural ectoderm development. Several signaling pathways cooperate during neural ectoderm development and in vitro differentiation of hPSCs toward neural cell lineages is also affected by them. In this study, we considered some of the known sources of these variable signaling cues arising from cell culture media components and sought to modulate their effects by applying a comprehensive combination of small molecules and growth factors for CO generation. Histological analysis demonstrated that these COs recapitulate the neural progenitor zone and early cortical layer organization, containing different types of neuronal and glial cells which was in accordance with single-nucleus transcriptome profiling results. Moreover, patch clamp and intracellular Ca(2+) dynamic studies demonstrated that the COs behave as a functional neural network. Thus, this method serves as a facile protocol for generating hPSC-derived COs that faithfully mimic the features of their in vivo counterparts in the developing human brain. See also Figure 1(Fig. 1). |
format | Online Article Text |
id | pubmed-10620858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-106208582023-11-03 A facile method to generate cerebral organoids from human pluripotent stem cells Simorgh, Susan Mousavi, Seyed Ahmad To, San Kit Pasque, Vincent Wierda, Keimpe Vervliet, Tim Yeganeh, Meghdad Pooyan, Paria Chai, Yoke Chin Verfaillie, Catherine Baharvand, Hossein EXCLI J Original Article Human cerebral organoids (COs) are self-organizing three-dimensional (3D) neural structures that provide a human-specific platform to study the cellular and molecular processes that underlie different neurological events. The first step of CO generation from human pluripotent stem cells (hPSCs) is neural induction, which is an in vitro simulation of neural ectoderm development. Several signaling pathways cooperate during neural ectoderm development and in vitro differentiation of hPSCs toward neural cell lineages is also affected by them. In this study, we considered some of the known sources of these variable signaling cues arising from cell culture media components and sought to modulate their effects by applying a comprehensive combination of small molecules and growth factors for CO generation. Histological analysis demonstrated that these COs recapitulate the neural progenitor zone and early cortical layer organization, containing different types of neuronal and glial cells which was in accordance with single-nucleus transcriptome profiling results. Moreover, patch clamp and intracellular Ca(2+) dynamic studies demonstrated that the COs behave as a functional neural network. Thus, this method serves as a facile protocol for generating hPSC-derived COs that faithfully mimic the features of their in vivo counterparts in the developing human brain. See also Figure 1(Fig. 1). Leibniz Research Centre for Working Environment and Human Factors 2023-10-05 /pmc/articles/PMC10620858/ /pubmed/37927348 http://dx.doi.org/10.17179/excli2023-6299 Text en Copyright © 2023 Simorgh et al. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Original Article Simorgh, Susan Mousavi, Seyed Ahmad To, San Kit Pasque, Vincent Wierda, Keimpe Vervliet, Tim Yeganeh, Meghdad Pooyan, Paria Chai, Yoke Chin Verfaillie, Catherine Baharvand, Hossein A facile method to generate cerebral organoids from human pluripotent stem cells |
title | A facile method to generate cerebral organoids from human pluripotent stem cells |
title_full | A facile method to generate cerebral organoids from human pluripotent stem cells |
title_fullStr | A facile method to generate cerebral organoids from human pluripotent stem cells |
title_full_unstemmed | A facile method to generate cerebral organoids from human pluripotent stem cells |
title_short | A facile method to generate cerebral organoids from human pluripotent stem cells |
title_sort | facile method to generate cerebral organoids from human pluripotent stem cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620858/ https://www.ncbi.nlm.nih.gov/pubmed/37927348 http://dx.doi.org/10.17179/excli2023-6299 |
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