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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...

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Autores principales: van der Plas, Thijs L, Tubiana, Jérôme, Le Goc, Guillaume, Migault, Geoffrey, Kunst, Michael, Baier, Herwig, Bormuth, Volker, Englitz, Bernhard, Debrégeas, Georges
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
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.
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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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