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Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions
Cortical neurons activated during recent experiences often reactivate with dorsal hippocampal CA1 sharp-wave ripples (SWRs) during subsequent rest. Less is known about cortical interactions with intermediate hippocampal CA1, whose connectivity, functions, and SWRs differ from those of dorsal CA1. We...
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/PMC10055189/ https://www.ncbi.nlm.nih.gov/pubmed/36993665 http://dx.doi.org/10.1101/2023.03.17.533028 |
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author | Jeong, Huijeong Namboodiri, Vijay Mohan K Jung, Min Whan Andermann, Mark L. |
author_facet | Jeong, Huijeong Namboodiri, Vijay Mohan K Jung, Min Whan Andermann, Mark L. |
author_sort | Jeong, Huijeong |
collection | PubMed |
description | Cortical neurons activated during recent experiences often reactivate with dorsal hippocampal CA1 sharp-wave ripples (SWRs) during subsequent rest. Less is known about cortical interactions with intermediate hippocampal CA1, whose connectivity, functions, and SWRs differ from those of dorsal CA1. We identified three clusters of visual cortical excitatory neurons that are excited together with either dorsal or intermediate CA1 SWRs, or suppressed before both SWRs. Neurons in each cluster were distributed across primary and higher visual cortices and co-active even in the absence of SWRs. These ensembles exhibited similar visual responses but different coupling to thalamus and pupil-indexed arousal. We observed a consistent activity sequence: (i) suppression of SWR-suppressed cortical neurons, (ii) thalamic silence, and (iii) activation of the cortical ensemble preceding and predicting intermediate CA1 SWRs. We propose that the coordinated dynamics of these ensembles relay visual experiences to distinct hippocampal subregions for incorporation into different cognitive maps. |
format | Online Article Text |
id | pubmed-10055189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100551892023-03-30 Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions Jeong, Huijeong Namboodiri, Vijay Mohan K Jung, Min Whan Andermann, Mark L. bioRxiv Article Cortical neurons activated during recent experiences often reactivate with dorsal hippocampal CA1 sharp-wave ripples (SWRs) during subsequent rest. Less is known about cortical interactions with intermediate hippocampal CA1, whose connectivity, functions, and SWRs differ from those of dorsal CA1. We identified three clusters of visual cortical excitatory neurons that are excited together with either dorsal or intermediate CA1 SWRs, or suppressed before both SWRs. Neurons in each cluster were distributed across primary and higher visual cortices and co-active even in the absence of SWRs. These ensembles exhibited similar visual responses but different coupling to thalamus and pupil-indexed arousal. We observed a consistent activity sequence: (i) suppression of SWR-suppressed cortical neurons, (ii) thalamic silence, and (iii) activation of the cortical ensemble preceding and predicting intermediate CA1 SWRs. We propose that the coordinated dynamics of these ensembles relay visual experiences to distinct hippocampal subregions for incorporation into different cognitive maps. Cold Spring Harbor Laboratory 2023-03-18 /pmc/articles/PMC10055189/ /pubmed/36993665 http://dx.doi.org/10.1101/2023.03.17.533028 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 Jeong, Huijeong Namboodiri, Vijay Mohan K Jung, Min Whan Andermann, Mark L. Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title | Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title_full | Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title_fullStr | Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title_full_unstemmed | Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title_short | Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
title_sort | sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055189/ https://www.ncbi.nlm.nih.gov/pubmed/36993665 http://dx.doi.org/10.1101/2023.03.17.533028 |
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