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Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity
Patterns of endogenous activity in the brain reflect a stochastic exploration of the neuronal state space that is constrained by the underlying assembly organization of neurons. Yet, it remains to be shown that this interplay between neurons and their assembly dynamics indeed suffices to generate wh...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940913/ https://www.ncbi.nlm.nih.gov/pubmed/36648065 http://dx.doi.org/10.7554/eLife.83139 |
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author | van der Plas, Thijs L Tubiana, Jérôme Le Goc, Guillaume Migault, Geoffrey Kunst, Michael Baier, Herwig Bormuth, Volker Englitz, Bernhard Debrégeas, Georges |
author_facet | van der Plas, Thijs L Tubiana, Jérôme Le Goc, Guillaume Migault, Geoffrey Kunst, Michael Baier, Herwig Bormuth, Volker Englitz, Bernhard Debrégeas, Georges |
author_sort | van der Plas, Thijs L |
collection | PubMed |
description | Patterns of endogenous activity in the brain reflect a stochastic exploration of the neuronal state space that is constrained by the underlying assembly organization of neurons. Yet, it remains to be shown that this interplay between neurons and their assembly dynamics indeed suffices to generate whole-brain data statistics. Here, we recorded the activity from ∼40,000 neurons simultaneously in zebrafish larvae, and show that a data-driven generative model of neuron-assembly interactions can accurately reproduce the mean activity and pairwise correlation statistics of their spontaneous activity. This model, the compositional Restricted Boltzmann Machine (cRBM), unveils ∼200 neural assemblies, which compose neurophysiological circuits and whose various combinations form successive brain states. We then performed in silico perturbation experiments to determine the interregional functional connectivity, which is conserved across individual animals and correlates well with structural connectivity. Our results showcase how cRBMs can capture the coarse-grained organization of the zebrafish brain. Notably, this generative model can readily be deployed to parse neural data obtained by other large-scale recording techniques. |
format | Online Article Text |
id | pubmed-9940913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99409132023-02-21 Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity van der Plas, Thijs L Tubiana, Jérôme Le Goc, Guillaume Migault, Geoffrey Kunst, Michael Baier, Herwig Bormuth, Volker Englitz, Bernhard Debrégeas, Georges eLife Neuroscience Patterns of endogenous activity in the brain reflect a stochastic exploration of the neuronal state space that is constrained by the underlying assembly organization of neurons. Yet, it remains to be shown that this interplay between neurons and their assembly dynamics indeed suffices to generate whole-brain data statistics. Here, we recorded the activity from ∼40,000 neurons simultaneously in zebrafish larvae, and show that a data-driven generative model of neuron-assembly interactions can accurately reproduce the mean activity and pairwise correlation statistics of their spontaneous activity. This model, the compositional Restricted Boltzmann Machine (cRBM), unveils ∼200 neural assemblies, which compose neurophysiological circuits and whose various combinations form successive brain states. We then performed in silico perturbation experiments to determine the interregional functional connectivity, which is conserved across individual animals and correlates well with structural connectivity. Our results showcase how cRBMs can capture the coarse-grained organization of the zebrafish brain. Notably, this generative model can readily be deployed to parse neural data obtained by other large-scale recording techniques. eLife Sciences Publications, Ltd 2023-01-17 /pmc/articles/PMC9940913/ /pubmed/36648065 http://dx.doi.org/10.7554/eLife.83139 Text en © 2023, van der Plas, Tubiana 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 | Neuroscience van der Plas, Thijs L Tubiana, Jérôme Le Goc, Guillaume Migault, Geoffrey Kunst, Michael Baier, Herwig Bormuth, Volker Englitz, Bernhard Debrégeas, Georges Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title | Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title_full | Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title_fullStr | Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title_full_unstemmed | Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title_short | Neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
title_sort | neural assemblies uncovered by generative modeling explain whole-brain activity statistics and reflect structural connectivity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9940913/ https://www.ncbi.nlm.nih.gov/pubmed/36648065 http://dx.doi.org/10.7554/eLife.83139 |
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