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Simulation of developing human neuronal cell networks
BACKGROUND: Microelectrode array (MEA) is a widely used technique to study for example the functional properties of neuronal networks derived from human embryonic stem cells (hESC-NN). With hESC-NN, we can investigate the earliest developmental stages of neuronal network formation in the human brain...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006268/ https://www.ncbi.nlm.nih.gov/pubmed/27576323 http://dx.doi.org/10.1186/s12938-016-0226-6 |
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author | Lenk, Kerstin Priwitzer, Barbara Ylä-Outinen, Laura Tietz, Lukas H. B. Narkilahti, Susanna Hyttinen, Jari A. K. |
author_facet | Lenk, Kerstin Priwitzer, Barbara Ylä-Outinen, Laura Tietz, Lukas H. B. Narkilahti, Susanna Hyttinen, Jari A. K. |
author_sort | Lenk, Kerstin |
collection | PubMed |
description | BACKGROUND: Microelectrode array (MEA) is a widely used technique to study for example the functional properties of neuronal networks derived from human embryonic stem cells (hESC-NN). With hESC-NN, we can investigate the earliest developmental stages of neuronal network formation in the human brain. METHODS: In this paper, we propose an in silico model of maturating hESC-NNs based on a phenomenological model called INEX. We focus on simulations of the development of bursts in hESC-NNs, which are the main feature of neuronal activation patterns. The model was developed with data from developing hESC-NN recordings on MEAs which showed increase in the neuronal activity during the investigated six measurement time points in the experimental and simulated data. RESULTS: Our simulations suggest that the maturation process of hESC-NN, resulting in the formation of bursts, can be explained by the development of synapses. Moreover, spike and burst rate both decreased at the last measurement time point suggesting a pruning of synapses as the weak ones are removed. CONCLUSIONS: To conclude, our model reflects the assumption that the interaction between excitatory and inhibitory neurons during the maturation of a neuronal network and the spontaneous emergence of bursts are due to increased connectivity caused by the forming of new synapses. |
format | Online Article Text |
id | pubmed-5006268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50062682016-09-01 Simulation of developing human neuronal cell networks Lenk, Kerstin Priwitzer, Barbara Ylä-Outinen, Laura Tietz, Lukas H. B. Narkilahti, Susanna Hyttinen, Jari A. K. Biomed Eng Online Research BACKGROUND: Microelectrode array (MEA) is a widely used technique to study for example the functional properties of neuronal networks derived from human embryonic stem cells (hESC-NN). With hESC-NN, we can investigate the earliest developmental stages of neuronal network formation in the human brain. METHODS: In this paper, we propose an in silico model of maturating hESC-NNs based on a phenomenological model called INEX. We focus on simulations of the development of bursts in hESC-NNs, which are the main feature of neuronal activation patterns. The model was developed with data from developing hESC-NN recordings on MEAs which showed increase in the neuronal activity during the investigated six measurement time points in the experimental and simulated data. RESULTS: Our simulations suggest that the maturation process of hESC-NN, resulting in the formation of bursts, can be explained by the development of synapses. Moreover, spike and burst rate both decreased at the last measurement time point suggesting a pruning of synapses as the weak ones are removed. CONCLUSIONS: To conclude, our model reflects the assumption that the interaction between excitatory and inhibitory neurons during the maturation of a neuronal network and the spontaneous emergence of bursts are due to increased connectivity caused by the forming of new synapses. BioMed Central 2016-08-30 /pmc/articles/PMC5006268/ /pubmed/27576323 http://dx.doi.org/10.1186/s12938-016-0226-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lenk, Kerstin Priwitzer, Barbara Ylä-Outinen, Laura Tietz, Lukas H. B. Narkilahti, Susanna Hyttinen, Jari A. K. Simulation of developing human neuronal cell networks |
title | Simulation of developing human neuronal cell networks |
title_full | Simulation of developing human neuronal cell networks |
title_fullStr | Simulation of developing human neuronal cell networks |
title_full_unstemmed | Simulation of developing human neuronal cell networks |
title_short | Simulation of developing human neuronal cell networks |
title_sort | simulation of developing human neuronal cell networks |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006268/ https://www.ncbi.nlm.nih.gov/pubmed/27576323 http://dx.doi.org/10.1186/s12938-016-0226-6 |
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