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Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids
Brain organoids are promising tools for disease modeling and drug development. For proper neuronal network formation excitatory and inhibitory neurons as well as glia need to co-develop. Here, we report the directed self-organization of human induced pluripotent stem cells in a collagen hydrogel tow...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391775/ https://www.ncbi.nlm.nih.gov/pubmed/32728089 http://dx.doi.org/10.1038/s41467-020-17521-w |
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author | Zafeiriou, Maria-Patapia Bao, Guobin Hudson, James Halder, Rashi Blenkle, Alica Schreiber, Marie-Kristin Fischer, Andre Schild, Detlev Zimmermann, Wolfram-Hubertus |
author_facet | Zafeiriou, Maria-Patapia Bao, Guobin Hudson, James Halder, Rashi Blenkle, Alica Schreiber, Marie-Kristin Fischer, Andre Schild, Detlev Zimmermann, Wolfram-Hubertus |
author_sort | Zafeiriou, Maria-Patapia |
collection | PubMed |
description | Brain organoids are promising tools for disease modeling and drug development. For proper neuronal network formation excitatory and inhibitory neurons as well as glia need to co-develop. Here, we report the directed self-organization of human induced pluripotent stem cells in a collagen hydrogel towards a highly interconnected neuronal network at a macroscale tissue format. Bioengineered Neuronal Organoids (BENOs) comprise interconnected excitatory and inhibitory neurons with supportive astrocytes and oligodendrocytes. Giant depolarizing potential (GDP)-like events observed in early BENO cultures mimic early network activity of the fetal brain. The observed GABA polarity switch and reduced GDPs in >40 day BENO indicate progressive neuronal network maturation. BENOs demonstrate expedited complex network burst development after two months and evidence for long-term potentiation. The similarity of structural and functional properties to the fetal brain may allow for the application of BENOs in studies of neuronal plasticity and modeling of disease. |
format | Online Article Text |
id | pubmed-7391775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73917752020-08-12 Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids Zafeiriou, Maria-Patapia Bao, Guobin Hudson, James Halder, Rashi Blenkle, Alica Schreiber, Marie-Kristin Fischer, Andre Schild, Detlev Zimmermann, Wolfram-Hubertus Nat Commun Article Brain organoids are promising tools for disease modeling and drug development. For proper neuronal network formation excitatory and inhibitory neurons as well as glia need to co-develop. Here, we report the directed self-organization of human induced pluripotent stem cells in a collagen hydrogel towards a highly interconnected neuronal network at a macroscale tissue format. Bioengineered Neuronal Organoids (BENOs) comprise interconnected excitatory and inhibitory neurons with supportive astrocytes and oligodendrocytes. Giant depolarizing potential (GDP)-like events observed in early BENO cultures mimic early network activity of the fetal brain. The observed GABA polarity switch and reduced GDPs in >40 day BENO indicate progressive neuronal network maturation. BENOs demonstrate expedited complex network burst development after two months and evidence for long-term potentiation. The similarity of structural and functional properties to the fetal brain may allow for the application of BENOs in studies of neuronal plasticity and modeling of disease. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7391775/ /pubmed/32728089 http://dx.doi.org/10.1038/s41467-020-17521-w 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zafeiriou, Maria-Patapia Bao, Guobin Hudson, James Halder, Rashi Blenkle, Alica Schreiber, Marie-Kristin Fischer, Andre Schild, Detlev Zimmermann, Wolfram-Hubertus Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title | Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title_full | Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title_fullStr | Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title_full_unstemmed | Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title_short | Developmental GABA polarity switch and neuronal plasticity in Bioengineered Neuronal Organoids |
title_sort | developmental gaba polarity switch and neuronal plasticity in bioengineered neuronal organoids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391775/ https://www.ncbi.nlm.nih.gov/pubmed/32728089 http://dx.doi.org/10.1038/s41467-020-17521-w |
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