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Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures
Reproducibly generating human induced pluripotent stem cell-based functional neuronal circuits, solely obtained from single individuals, poses particular challenges to achieve personalized and patient specific functional neuronal in vitro models. A hallmark of functional neuronal assemblies, synchro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491690/ https://www.ncbi.nlm.nih.gov/pubmed/31068774 http://dx.doi.org/10.3389/fnins.2019.00351 |
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author | Izsak, Julia Seth, Henrik Andersson, Mats Vizlin-Hodzic, Dzeneta Theiss, Stephan Hanse, Eric Ågren, Hans Funa, Keiko Illes, Sebastian |
author_facet | Izsak, Julia Seth, Henrik Andersson, Mats Vizlin-Hodzic, Dzeneta Theiss, Stephan Hanse, Eric Ågren, Hans Funa, Keiko Illes, Sebastian |
author_sort | Izsak, Julia |
collection | PubMed |
description | Reproducibly generating human induced pluripotent stem cell-based functional neuronal circuits, solely obtained from single individuals, poses particular challenges to achieve personalized and patient specific functional neuronal in vitro models. A hallmark of functional neuronal assemblies, synchronous neuronal activity, can be non-invasively studied by microelectrode array (MEA) technology, reliably capturing physiological and pathophysiological aspects of human brain function. In our here presented manuscript, we demonstrate a procedure to generate 3D neural aggregates comprising astrocytes, oligodendroglial cells, and neurons obtained from the same human tissue sample. Moreover, we demonstrate the robust ability of those neurons to create a highly synchronously active neuronal network within 3 weeks in vitro, without additionally applied astrocytes. The fusion of MEA-technology with functional neuronal circuits solely obtained from one individual’s cells represent isogenic person-specific human neuronal sensor chips that pave the way for specific personalized in vitro neuronal networks as well as neurological and neuropsychiatric disease modeling. |
format | Online Article Text |
id | pubmed-6491690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64916902019-05-08 Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures Izsak, Julia Seth, Henrik Andersson, Mats Vizlin-Hodzic, Dzeneta Theiss, Stephan Hanse, Eric Ågren, Hans Funa, Keiko Illes, Sebastian Front Neurosci Neuroscience Reproducibly generating human induced pluripotent stem cell-based functional neuronal circuits, solely obtained from single individuals, poses particular challenges to achieve personalized and patient specific functional neuronal in vitro models. A hallmark of functional neuronal assemblies, synchronous neuronal activity, can be non-invasively studied by microelectrode array (MEA) technology, reliably capturing physiological and pathophysiological aspects of human brain function. In our here presented manuscript, we demonstrate a procedure to generate 3D neural aggregates comprising astrocytes, oligodendroglial cells, and neurons obtained from the same human tissue sample. Moreover, we demonstrate the robust ability of those neurons to create a highly synchronously active neuronal network within 3 weeks in vitro, without additionally applied astrocytes. The fusion of MEA-technology with functional neuronal circuits solely obtained from one individual’s cells represent isogenic person-specific human neuronal sensor chips that pave the way for specific personalized in vitro neuronal networks as well as neurological and neuropsychiatric disease modeling. Frontiers Media S.A. 2019-04-24 /pmc/articles/PMC6491690/ /pubmed/31068774 http://dx.doi.org/10.3389/fnins.2019.00351 Text en Copyright © 2019 Izsak, Seth, Andersson, Vizlin-Hodzic, Theiss, Hanse, Ågren, Funa and Illes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Izsak, Julia Seth, Henrik Andersson, Mats Vizlin-Hodzic, Dzeneta Theiss, Stephan Hanse, Eric Ågren, Hans Funa, Keiko Illes, Sebastian Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title | Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title_full | Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title_fullStr | Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title_full_unstemmed | Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title_short | Robust Generation of Person-Specific, Synchronously Active Neuronal Networks Using Purely Isogenic Human iPSC-3D Neural Aggregate Cultures |
title_sort | robust generation of person-specific, synchronously active neuronal networks using purely isogenic human ipsc-3d neural aggregate cultures |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491690/ https://www.ncbi.nlm.nih.gov/pubmed/31068774 http://dx.doi.org/10.3389/fnins.2019.00351 |
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