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In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment
Neurons differentiated from induced pluripotent stem cells (iPSCs) typically show regular spiking and synaptic activity but lack more complex network activity critical for brain development, such as periodic depolarizations including simultaneous involvement of glutamatergic and GABAergic neurotrans...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363884/ https://www.ncbi.nlm.nih.gov/pubmed/32559460 http://dx.doi.org/10.1016/j.stemcr.2020.05.015 |
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author | Rosa, Filip Dhingra, Ashutosh Uysal, Betül Mendis, G. Dulini C. Loeffler, Heidi Elsen, Gina Mueller, Stephan Schwarz, Niklas Castillo-Lizardo, Melissa Cuddy, Claire Becker, Felicitas Heutink, Peter Reid, Christopher A. Petrou, Steven Lerche, Holger Maljevic, Snezana |
author_facet | Rosa, Filip Dhingra, Ashutosh Uysal, Betül Mendis, G. Dulini C. Loeffler, Heidi Elsen, Gina Mueller, Stephan Schwarz, Niklas Castillo-Lizardo, Melissa Cuddy, Claire Becker, Felicitas Heutink, Peter Reid, Christopher A. Petrou, Steven Lerche, Holger Maljevic, Snezana |
author_sort | Rosa, Filip |
collection | PubMed |
description | Neurons differentiated from induced pluripotent stem cells (iPSCs) typically show regular spiking and synaptic activity but lack more complex network activity critical for brain development, such as periodic depolarizations including simultaneous involvement of glutamatergic and GABAergic neurotransmission. We generated human iPSC-derived neurons exhibiting spontaneous oscillatory activity after cultivation of up to 6 months, which resembles early oscillations observed in rodent neurons. This behavior was found in neurons generated using a more “native” embryoid body protocol, in contrast to a “fast” protocol based on NGN2 overexpression. A comparison with published data indicates that EB-derived neurons reach the maturity of neurons of the third trimester and NGN2-derived neurons of the second trimester of human gestation. Co-culturing NGN2-derived neurons with astrocytes only led to a partial compensation and did not reliably induce complex network activity. Our data will help selection of the appropriate iPSC differentiation assay to address specific questions related to neurodevelopmental disorders. |
format | Online Article Text |
id | pubmed-7363884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73638842020-07-20 In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment Rosa, Filip Dhingra, Ashutosh Uysal, Betül Mendis, G. Dulini C. Loeffler, Heidi Elsen, Gina Mueller, Stephan Schwarz, Niklas Castillo-Lizardo, Melissa Cuddy, Claire Becker, Felicitas Heutink, Peter Reid, Christopher A. Petrou, Steven Lerche, Holger Maljevic, Snezana Stem Cell Reports Article Neurons differentiated from induced pluripotent stem cells (iPSCs) typically show regular spiking and synaptic activity but lack more complex network activity critical for brain development, such as periodic depolarizations including simultaneous involvement of glutamatergic and GABAergic neurotransmission. We generated human iPSC-derived neurons exhibiting spontaneous oscillatory activity after cultivation of up to 6 months, which resembles early oscillations observed in rodent neurons. This behavior was found in neurons generated using a more “native” embryoid body protocol, in contrast to a “fast” protocol based on NGN2 overexpression. A comparison with published data indicates that EB-derived neurons reach the maturity of neurons of the third trimester and NGN2-derived neurons of the second trimester of human gestation. Co-culturing NGN2-derived neurons with astrocytes only led to a partial compensation and did not reliably induce complex network activity. Our data will help selection of the appropriate iPSC differentiation assay to address specific questions related to neurodevelopmental disorders. Elsevier 2020-06-18 /pmc/articles/PMC7363884/ /pubmed/32559460 http://dx.doi.org/10.1016/j.stemcr.2020.05.015 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Rosa, Filip Dhingra, Ashutosh Uysal, Betül Mendis, G. Dulini C. Loeffler, Heidi Elsen, Gina Mueller, Stephan Schwarz, Niklas Castillo-Lizardo, Melissa Cuddy, Claire Becker, Felicitas Heutink, Peter Reid, Christopher A. Petrou, Steven Lerche, Holger Maljevic, Snezana In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title | In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title_full | In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title_fullStr | In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title_full_unstemmed | In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title_short | In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment |
title_sort | in vitro differentiated human stem cell-derived neurons reproduce synaptic synchronicity arising during neurodevelopment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363884/ https://www.ncbi.nlm.nih.gov/pubmed/32559460 http://dx.doi.org/10.1016/j.stemcr.2020.05.015 |
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