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Synchronous activity patterns in the dentate gyrus during immobility

The hippocampal dentate gyrus is an important relay conveying sensory information from the entorhinal cortex to the hippocampus proper. During exploration, the dentate gyrus has been proposed to act as a pattern separator. However, the dentate gyrus also shows structured activity during immobility a...

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Autores principales: Pofahl, Martin, Nikbakht, Negar, Haubrich, André N, Nguyen, Theresa, Masala, Nicola, Distler, Fabian, Braganza, Oliver, Macke, Jakob H, Ewell, Laura A, Golcuk, Kurtulus, Beck, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987346/
https://www.ncbi.nlm.nih.gov/pubmed/33709911
http://dx.doi.org/10.7554/eLife.65786
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author Pofahl, Martin
Nikbakht, Negar
Haubrich, André N
Nguyen, Theresa
Masala, Nicola
Distler, Fabian
Braganza, Oliver
Macke, Jakob H
Ewell, Laura A
Golcuk, Kurtulus
Beck, Heinz
author_facet Pofahl, Martin
Nikbakht, Negar
Haubrich, André N
Nguyen, Theresa
Masala, Nicola
Distler, Fabian
Braganza, Oliver
Macke, Jakob H
Ewell, Laura A
Golcuk, Kurtulus
Beck, Heinz
author_sort Pofahl, Martin
collection PubMed
description The hippocampal dentate gyrus is an important relay conveying sensory information from the entorhinal cortex to the hippocampus proper. During exploration, the dentate gyrus has been proposed to act as a pattern separator. However, the dentate gyrus also shows structured activity during immobility and sleep. The properties of these activity patterns at cellular resolution, and their role in hippocampal-dependent memory processes have remained unclear. Using dual-color in vivo two-photon Ca(2+) imaging, we show that in immobile mice dentate granule cells generate sparse, synchronized activity patterns associated with entorhinal cortex activation. These population events are structured and modified by changes in the environment; and they incorporate place- and speed cells. Importantly, they are more similar than expected by chance to population patterns evoked during self-motion. Using optogenetic inhibition, we show that granule cell activity is not only required during exploration, but also during immobility in order to form dentate gyrus-dependent spatial memories.
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spelling pubmed-79873462021-03-24 Synchronous activity patterns in the dentate gyrus during immobility Pofahl, Martin Nikbakht, Negar Haubrich, André N Nguyen, Theresa Masala, Nicola Distler, Fabian Braganza, Oliver Macke, Jakob H Ewell, Laura A Golcuk, Kurtulus Beck, Heinz eLife Neuroscience The hippocampal dentate gyrus is an important relay conveying sensory information from the entorhinal cortex to the hippocampus proper. During exploration, the dentate gyrus has been proposed to act as a pattern separator. However, the dentate gyrus also shows structured activity during immobility and sleep. The properties of these activity patterns at cellular resolution, and their role in hippocampal-dependent memory processes have remained unclear. Using dual-color in vivo two-photon Ca(2+) imaging, we show that in immobile mice dentate granule cells generate sparse, synchronized activity patterns associated with entorhinal cortex activation. These population events are structured and modified by changes in the environment; and they incorporate place- and speed cells. Importantly, they are more similar than expected by chance to population patterns evoked during self-motion. Using optogenetic inhibition, we show that granule cell activity is not only required during exploration, but also during immobility in order to form dentate gyrus-dependent spatial memories. eLife Sciences Publications, Ltd 2021-03-12 /pmc/articles/PMC7987346/ /pubmed/33709911 http://dx.doi.org/10.7554/eLife.65786 Text en © 2021, Pofahl et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Pofahl, Martin
Nikbakht, Negar
Haubrich, André N
Nguyen, Theresa
Masala, Nicola
Distler, Fabian
Braganza, Oliver
Macke, Jakob H
Ewell, Laura A
Golcuk, Kurtulus
Beck, Heinz
Synchronous activity patterns in the dentate gyrus during immobility
title Synchronous activity patterns in the dentate gyrus during immobility
title_full Synchronous activity patterns in the dentate gyrus during immobility
title_fullStr Synchronous activity patterns in the dentate gyrus during immobility
title_full_unstemmed Synchronous activity patterns in the dentate gyrus during immobility
title_short Synchronous activity patterns in the dentate gyrus during immobility
title_sort synchronous activity patterns in the dentate gyrus during immobility
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987346/
https://www.ncbi.nlm.nih.gov/pubmed/33709911
http://dx.doi.org/10.7554/eLife.65786
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