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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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