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Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters
Brains demonstrate varying spatial scales of nested hierarchical clustering. Identifying the brain’s neuronal cluster size to be presented as nodes in a network computation is critical to both neuroscience and artificial intelligence, as these define the cognitive blocks capable of building intellig...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936002/ https://www.ncbi.nlm.nih.gov/pubmed/33674620 http://dx.doi.org/10.1038/s41598-021-82461-4 |
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author | Amgalan, Anar Taylor, Patrick Mujica-Parodi, Lilianne R. Siegelmann, Hava T. |
author_facet | Amgalan, Anar Taylor, Patrick Mujica-Parodi, Lilianne R. Siegelmann, Hava T. |
author_sort | Amgalan, Anar |
collection | PubMed |
description | Brains demonstrate varying spatial scales of nested hierarchical clustering. Identifying the brain’s neuronal cluster size to be presented as nodes in a network computation is critical to both neuroscience and artificial intelligence, as these define the cognitive blocks capable of building intelligent computation. Experiments support various forms and sizes of neural clustering, from handfuls of dendrites to thousands of neurons, and hint at their behavior. Here, we use computational simulations with a brain-derived fMRI network to show that not only do brain networks remain structurally self-similar across scales but also neuron-like signal integration functionality (“integrate and fire”) is preserved at particular clustering scales. As such, we propose a coarse-graining of neuronal networks to ensemble-nodes, with multiple spikes making up its ensemble-spike and time re-scaling factor defining its ensemble-time step. This fractal-like spatiotemporal property, observed in both structure and function, permits strategic choice in bridging across experimental scales for computational modeling while also suggesting regulatory constraints on developmental and evolutionary “growth spurts” in brain size, as per punctuated equilibrium theories in evolutionary biology. |
format | Online Article Text |
id | pubmed-7936002 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79360022021-03-08 Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters Amgalan, Anar Taylor, Patrick Mujica-Parodi, Lilianne R. Siegelmann, Hava T. Sci Rep Article Brains demonstrate varying spatial scales of nested hierarchical clustering. Identifying the brain’s neuronal cluster size to be presented as nodes in a network computation is critical to both neuroscience and artificial intelligence, as these define the cognitive blocks capable of building intelligent computation. Experiments support various forms and sizes of neural clustering, from handfuls of dendrites to thousands of neurons, and hint at their behavior. Here, we use computational simulations with a brain-derived fMRI network to show that not only do brain networks remain structurally self-similar across scales but also neuron-like signal integration functionality (“integrate and fire”) is preserved at particular clustering scales. As such, we propose a coarse-graining of neuronal networks to ensemble-nodes, with multiple spikes making up its ensemble-spike and time re-scaling factor defining its ensemble-time step. This fractal-like spatiotemporal property, observed in both structure and function, permits strategic choice in bridging across experimental scales for computational modeling while also suggesting regulatory constraints on developmental and evolutionary “growth spurts” in brain size, as per punctuated equilibrium theories in evolutionary biology. Nature Publishing Group UK 2021-03-05 /pmc/articles/PMC7936002/ /pubmed/33674620 http://dx.doi.org/10.1038/s41598-021-82461-4 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Amgalan, Anar Taylor, Patrick Mujica-Parodi, Lilianne R. Siegelmann, Hava T. Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title | Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title_full | Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title_fullStr | Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title_full_unstemmed | Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title_short | Unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
title_sort | unique scales preserve self-similar integrate-and-fire functionality of neuronal clusters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936002/ https://www.ncbi.nlm.nih.gov/pubmed/33674620 http://dx.doi.org/10.1038/s41598-021-82461-4 |
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