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Early lock-in of structured and specialised information flows during neural development
The brains of many organisms are capable of complicated distributed computation underpinned by a highly advanced information processing capacity. Although substantial progress has been made towards characterising the information flow component of this capacity in mature brains, there is a distinct l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064303/ https://www.ncbi.nlm.nih.gov/pubmed/35286256 http://dx.doi.org/10.7554/eLife.74651 |
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author | Shorten, David P Priesemann, Viola Wibral, Michael Lizier, Joseph T |
author_facet | Shorten, David P Priesemann, Viola Wibral, Michael Lizier, Joseph T |
author_sort | Shorten, David P |
collection | PubMed |
description | The brains of many organisms are capable of complicated distributed computation underpinned by a highly advanced information processing capacity. Although substantial progress has been made towards characterising the information flow component of this capacity in mature brains, there is a distinct lack of work characterising its emergence during neural development. This lack of progress has been largely driven by the lack of effective estimators of information processing operations for spiking data. Here, we leverage recent advances in this estimation task in order to quantify the changes in transfer entropy during development. We do so by studying the changes in the intrinsic dynamics of the spontaneous activity of developing dissociated neural cell cultures. We find that the quantity of information flowing across these networks undergoes a dramatic increase across development. Moreover, the spatial structure of these flows exhibits a tendency to lock-in at the point when they arise. We also characterise the flow of information during the crucial periods of population bursts. We find that, during these bursts, nodes tend to undertake specialised computational roles as either transmitters, mediators, or receivers of information, with these roles tending to align with their average spike ordering. Further, we find that these roles are regularly locked-in when the information flows are established. Finally, we compare these results to information flows in a model network developing according to a spike-timing-dependent plasticity learning rule. Similar temporal patterns in the development of information flows were observed in these networks, hinting at the broader generality of these phenomena. |
format | Online Article Text |
id | pubmed-9064303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-90643032022-05-04 Early lock-in of structured and specialised information flows during neural development Shorten, David P Priesemann, Viola Wibral, Michael Lizier, Joseph T eLife Computational and Systems Biology The brains of many organisms are capable of complicated distributed computation underpinned by a highly advanced information processing capacity. Although substantial progress has been made towards characterising the information flow component of this capacity in mature brains, there is a distinct lack of work characterising its emergence during neural development. This lack of progress has been largely driven by the lack of effective estimators of information processing operations for spiking data. Here, we leverage recent advances in this estimation task in order to quantify the changes in transfer entropy during development. We do so by studying the changes in the intrinsic dynamics of the spontaneous activity of developing dissociated neural cell cultures. We find that the quantity of information flowing across these networks undergoes a dramatic increase across development. Moreover, the spatial structure of these flows exhibits a tendency to lock-in at the point when they arise. We also characterise the flow of information during the crucial periods of population bursts. We find that, during these bursts, nodes tend to undertake specialised computational roles as either transmitters, mediators, or receivers of information, with these roles tending to align with their average spike ordering. Further, we find that these roles are regularly locked-in when the information flows are established. Finally, we compare these results to information flows in a model network developing according to a spike-timing-dependent plasticity learning rule. Similar temporal patterns in the development of information flows were observed in these networks, hinting at the broader generality of these phenomena. eLife Sciences Publications, Ltd 2022-03-14 /pmc/articles/PMC9064303/ /pubmed/35286256 http://dx.doi.org/10.7554/eLife.74651 Text en © 2022, Shorten et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Shorten, David P Priesemann, Viola Wibral, Michael Lizier, Joseph T Early lock-in of structured and specialised information flows during neural development |
title | Early lock-in of structured and specialised information flows during neural development |
title_full | Early lock-in of structured and specialised information flows during neural development |
title_fullStr | Early lock-in of structured and specialised information flows during neural development |
title_full_unstemmed | Early lock-in of structured and specialised information flows during neural development |
title_short | Early lock-in of structured and specialised information flows during neural development |
title_sort | early lock-in of structured and specialised information flows during neural development |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064303/ https://www.ncbi.nlm.nih.gov/pubmed/35286256 http://dx.doi.org/10.7554/eLife.74651 |
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