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Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data
Understanding the mechanisms by which neurons create or suppress connections to enable communication in brain-derived neuronal cultures can inform how learning, cognition and creative behavior emerge. While prior studies have shown that neuronal cultures possess self-organizing criticality propertie...
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/PMC7492189/ https://www.ncbi.nlm.nih.gov/pubmed/32934305 http://dx.doi.org/10.1038/s41598-020-72013-7 |
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author | Yin, Chenzhong Xiao, Xiongye Balaban, Valeriu Kandel, Mikhail E. Lee, Young Jae Popescu, Gabriel Bogdan, Paul |
author_facet | Yin, Chenzhong Xiao, Xiongye Balaban, Valeriu Kandel, Mikhail E. Lee, Young Jae Popescu, Gabriel Bogdan, Paul |
author_sort | Yin, Chenzhong |
collection | PubMed |
description | Understanding the mechanisms by which neurons create or suppress connections to enable communication in brain-derived neuronal cultures can inform how learning, cognition and creative behavior emerge. While prior studies have shown that neuronal cultures possess self-organizing criticality properties, we further demonstrate that in vitro brain-derived neuronal cultures exhibit a self-optimization phenomenon. More precisely, we analyze the multiscale neural growth data obtained from label-free quantitative microscopic imaging experiments and reconstruct the in vitro neuronal culture networks (microscale) and neuronal culture cluster networks (mesoscale). We investigate the structure and evolution of neuronal culture networks and neuronal culture cluster networks by estimating the importance of each network node and their information flow. By analyzing the degree-, closeness-, and betweenness-centrality, the node-to-node degree distribution (informing on neuronal interconnection phenomena), the clustering coefficient/transitivity (assessing the “small-world” properties), and the multifractal spectrum, we demonstrate that murine neurons exhibit self-optimizing behavior over time with topological characteristics distinct from existing complex network models. The time-evolving interconnection among murine neurons optimizes the network information flow, network robustness, and self-organization degree. These findings have complex implications for modeling neuronal cultures and potentially on how to design biological inspired artificial intelligence. |
format | Online Article Text |
id | pubmed-7492189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74921892020-09-16 Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data Yin, Chenzhong Xiao, Xiongye Balaban, Valeriu Kandel, Mikhail E. Lee, Young Jae Popescu, Gabriel Bogdan, Paul Sci Rep Article Understanding the mechanisms by which neurons create or suppress connections to enable communication in brain-derived neuronal cultures can inform how learning, cognition and creative behavior emerge. While prior studies have shown that neuronal cultures possess self-organizing criticality properties, we further demonstrate that in vitro brain-derived neuronal cultures exhibit a self-optimization phenomenon. More precisely, we analyze the multiscale neural growth data obtained from label-free quantitative microscopic imaging experiments and reconstruct the in vitro neuronal culture networks (microscale) and neuronal culture cluster networks (mesoscale). We investigate the structure and evolution of neuronal culture networks and neuronal culture cluster networks by estimating the importance of each network node and their information flow. By analyzing the degree-, closeness-, and betweenness-centrality, the node-to-node degree distribution (informing on neuronal interconnection phenomena), the clustering coefficient/transitivity (assessing the “small-world” properties), and the multifractal spectrum, we demonstrate that murine neurons exhibit self-optimizing behavior over time with topological characteristics distinct from existing complex network models. The time-evolving interconnection among murine neurons optimizes the network information flow, network robustness, and self-organization degree. These findings have complex implications for modeling neuronal cultures and potentially on how to design biological inspired artificial intelligence. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7492189/ /pubmed/32934305 http://dx.doi.org/10.1038/s41598-020-72013-7 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 Yin, Chenzhong Xiao, Xiongye Balaban, Valeriu Kandel, Mikhail E. Lee, Young Jae Popescu, Gabriel Bogdan, Paul Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title | Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title_full | Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title_fullStr | Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title_full_unstemmed | Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title_short | Network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
title_sort | network science characteristics of brain-derived neuronal cultures deciphered from quantitative phase imaging data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492189/ https://www.ncbi.nlm.nih.gov/pubmed/32934305 http://dx.doi.org/10.1038/s41598-020-72013-7 |
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