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Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions

View ORCID ProfileHuijeong Jeong, Vijay Mohan K Namboodiri, Min Whan Jung, Mark L. Andermann
doi: https://doi.org/10.1101/2023.03.17.533028
Huijeong Jeong
1Department of Neurology, University of California, San Francisco, CA 94158, USA
4Center for Synaptic Brain Dysfunctions, Institute for Basic Science, Daejeon 34141, Korea
5Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea
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  • ORCID record for Huijeong Jeong
Vijay Mohan K Namboodiri
1Department of Neurology, University of California, San Francisco, CA 94158, USA
2Neuroscience Graduate Program, University of California, San Francisco, CA 94158, USA
3Weill Institute for Neuroscience, Kavli Institute for Fundamental Neuroscience, Center for Integrative Neuroscience, University of California, San Francisco 94158, CA, USA
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  • For correspondence: [email protected] [email protected] [email protected]
Min Whan Jung
4Center for Synaptic Brain Dysfunctions, Institute for Basic Science, Daejeon 34141, Korea
5Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea
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  • For correspondence: [email protected] [email protected] [email protected]
Mark L. Andermann
6Division of Endocrinology, Metabolism, and Diabetes, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115 USA
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  • For correspondence: [email protected] [email protected] [email protected]
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Abstract

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.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted March 18, 2023.
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Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions
Huijeong Jeong, Vijay Mohan K Namboodiri, Min Whan Jung, Mark L. Andermann
bioRxiv 2023.03.17.533028; doi: https://doi.org/10.1101/2023.03.17.533028
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Sensory cortical ensembles exhibit differential coupling to ripples in distinct hippocampal subregions
Huijeong Jeong, Vijay Mohan K Namboodiri, Min Whan Jung, Mark L. Andermann
bioRxiv 2023.03.17.533028; doi: https://doi.org/10.1101/2023.03.17.533028

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