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The mechanics of correlated variability in segregated cortical excitatory subnetworks
Understanding the genesis of shared trial-to-trial variability in neural activity within sensory cortex is critical to uncovering the biological basis of information processing in the brain. Shared variability is often a reflection of the structure of cortical connectivity since this variability lik...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168290/ https://www.ncbi.nlm.nih.gov/pubmed/37162867 http://dx.doi.org/10.1101/2023.04.25.538323 |
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author | Negrón, Alex Getz, Matthew P. Handy, Gregory Doiron, Brent |
author_facet | Negrón, Alex Getz, Matthew P. Handy, Gregory Doiron, Brent |
author_sort | Negrón, Alex |
collection | PubMed |
description | Understanding the genesis of shared trial-to-trial variability in neural activity within sensory cortex is critical to uncovering the biological basis of information processing in the brain. Shared variability is often a reflection of the structure of cortical connectivity since this variability likely arises, in part, from local circuit inputs. A series of experiments from segregated networks of (excitatory) pyramidal neurons in mouse primary visual cortex challenge this view. Specifically, the across-network correlations were found to be larger than predicted given the known weak cross-network connectivity. We aim to uncover the circuit mechanisms responsible for these enhanced correlations through biologically motivated cortical circuit models. Our central finding is that coupling each excitatory subpopulation with a specific inhibitory subpopulation provides the most robust network-intrinsic solution in shaping these enhanced correlations. This result argues for the existence of excitatory-inhibitory functional assemblies in early sensory areas which mirror not just response properties but also connectivity between pyramidal cells. |
format | Online Article Text |
id | pubmed-10168290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101682902023-05-10 The mechanics of correlated variability in segregated cortical excitatory subnetworks Negrón, Alex Getz, Matthew P. Handy, Gregory Doiron, Brent bioRxiv Article Understanding the genesis of shared trial-to-trial variability in neural activity within sensory cortex is critical to uncovering the biological basis of information processing in the brain. Shared variability is often a reflection of the structure of cortical connectivity since this variability likely arises, in part, from local circuit inputs. A series of experiments from segregated networks of (excitatory) pyramidal neurons in mouse primary visual cortex challenge this view. Specifically, the across-network correlations were found to be larger than predicted given the known weak cross-network connectivity. We aim to uncover the circuit mechanisms responsible for these enhanced correlations through biologically motivated cortical circuit models. Our central finding is that coupling each excitatory subpopulation with a specific inhibitory subpopulation provides the most robust network-intrinsic solution in shaping these enhanced correlations. This result argues for the existence of excitatory-inhibitory functional assemblies in early sensory areas which mirror not just response properties but also connectivity between pyramidal cells. Cold Spring Harbor Laboratory 2023-04-27 /pmc/articles/PMC10168290/ /pubmed/37162867 http://dx.doi.org/10.1101/2023.04.25.538323 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Negrón, Alex Getz, Matthew P. Handy, Gregory Doiron, Brent The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title | The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title_full | The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title_fullStr | The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title_full_unstemmed | The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title_short | The mechanics of correlated variability in segregated cortical excitatory subnetworks |
title_sort | mechanics of correlated variability in segregated cortical excitatory subnetworks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168290/ https://www.ncbi.nlm.nih.gov/pubmed/37162867 http://dx.doi.org/10.1101/2023.04.25.538323 |
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