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Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics

Recent studies have found dramatic cell-type specific responses to stimulus novelty, highlighting the importance of analyzing the cortical circuitry at the cell-type specific level of granularity to understand brain function. Although initial work classified and characterized activity for each cell...

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Autores principales: Ito, Shinya, Piet, Alex, Bennett, Corbett, Durand, Séverine, Belski, Hannah, Garrett, Marina, Olsen, Shawn R., Arkhipov, Anton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634721/
https://www.ncbi.nlm.nih.gov/pubmed/37961331
http://dx.doi.org/10.1101/2023.10.21.563440
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author Ito, Shinya
Piet, Alex
Bennett, Corbett
Durand, Séverine
Belski, Hannah
Garrett, Marina
Olsen, Shawn R.
Arkhipov, Anton
author_facet Ito, Shinya
Piet, Alex
Bennett, Corbett
Durand, Séverine
Belski, Hannah
Garrett, Marina
Olsen, Shawn R.
Arkhipov, Anton
author_sort Ito, Shinya
collection PubMed
description Recent studies have found dramatic cell-type specific responses to stimulus novelty, highlighting the importance of analyzing the cortical circuitry at the cell-type specific level of granularity to understand brain function. Although initial work classified and characterized activity for each cell type, the specific alterations in cortical circuitry—particularly when multiple novelty effects interact—remain unclear. To address this gap, we employed a large-scale public dataset of electrophysiological recordings in the visual cortex of awake, behaving mice using Neuropixels probes and designed population network models to investigate the observed changes in neural dynamics in response to a combination of distinct forms of novelty. The model parameters were rigorously constrained by publicly available structural datasets, including multi-patch synaptic physiology and electron microscopy data. Our systematic optimization approach identified tens of thousands of model parameter sets that replicate the observed neural activity. Analysis of these solutions revealed generally weaker connections under novel stimuli, as well as a shift in the balance e between SST and VIP populations. Along with this, PV and SST populations experienced overall more excitatory influences compared to excitatory and VIP populations. Our results also highlight the role of VIP neurons in multiple aspects of visual stimulus processing and altering gain and saturation dynamics under novel conditions. In sum, our findings provide a systematic characterization of how the cortical circuit adapts to stimulus novelty by combining multiple rich public datasets.
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spelling pubmed-106347212023-11-13 Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics Ito, Shinya Piet, Alex Bennett, Corbett Durand, Séverine Belski, Hannah Garrett, Marina Olsen, Shawn R. Arkhipov, Anton bioRxiv Article Recent studies have found dramatic cell-type specific responses to stimulus novelty, highlighting the importance of analyzing the cortical circuitry at the cell-type specific level of granularity to understand brain function. Although initial work classified and characterized activity for each cell type, the specific alterations in cortical circuitry—particularly when multiple novelty effects interact—remain unclear. To address this gap, we employed a large-scale public dataset of electrophysiological recordings in the visual cortex of awake, behaving mice using Neuropixels probes and designed population network models to investigate the observed changes in neural dynamics in response to a combination of distinct forms of novelty. The model parameters were rigorously constrained by publicly available structural datasets, including multi-patch synaptic physiology and electron microscopy data. Our systematic optimization approach identified tens of thousands of model parameter sets that replicate the observed neural activity. Analysis of these solutions revealed generally weaker connections under novel stimuli, as well as a shift in the balance e between SST and VIP populations. Along with this, PV and SST populations experienced overall more excitatory influences compared to excitatory and VIP populations. Our results also highlight the role of VIP neurons in multiple aspects of visual stimulus processing and altering gain and saturation dynamics under novel conditions. In sum, our findings provide a systematic characterization of how the cortical circuit adapts to stimulus novelty by combining multiple rich public datasets. Cold Spring Harbor Laboratory 2023-10-23 /pmc/articles/PMC10634721/ /pubmed/37961331 http://dx.doi.org/10.1101/2023.10.21.563440 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
Ito, Shinya
Piet, Alex
Bennett, Corbett
Durand, Séverine
Belski, Hannah
Garrett, Marina
Olsen, Shawn R.
Arkhipov, Anton
Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title_full Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title_fullStr Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title_full_unstemmed Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title_short Coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
title_sort coordinated changes in a cortical circuit sculpt effects of novelty on neural dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634721/
https://www.ncbi.nlm.nih.gov/pubmed/37961331
http://dx.doi.org/10.1101/2023.10.21.563440
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