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Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles

Previous gain-of-function studies using an optogenetic technique showed that manipulation of the hippocampal dentate gyrus or CA1 cell ensembles is important for memory reactivation and to generate synthetic or false memory. However, gain-of-function study manipulating CA3 cell ensembles has not bee...

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Autores principales: Oishi, Naoya, Nomoto, Masanori, Ohkawa, Noriaki, Saitoh, Yoshito, Sano, Yoshitake, Tsujimura, Shuhei, Nishizono, Hirofumi, Matsuo, Mina, Muramatsu, Shin-ichi, Inokuchi, Kaoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323779/
https://www.ncbi.nlm.nih.gov/pubmed/30621738
http://dx.doi.org/10.1186/s13041-018-0424-1
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author Oishi, Naoya
Nomoto, Masanori
Ohkawa, Noriaki
Saitoh, Yoshito
Sano, Yoshitake
Tsujimura, Shuhei
Nishizono, Hirofumi
Matsuo, Mina
Muramatsu, Shin-ichi
Inokuchi, Kaoru
author_facet Oishi, Naoya
Nomoto, Masanori
Ohkawa, Noriaki
Saitoh, Yoshito
Sano, Yoshitake
Tsujimura, Shuhei
Nishizono, Hirofumi
Matsuo, Mina
Muramatsu, Shin-ichi
Inokuchi, Kaoru
author_sort Oishi, Naoya
collection PubMed
description Previous gain-of-function studies using an optogenetic technique showed that manipulation of the hippocampal dentate gyrus or CA1 cell ensembles is important for memory reactivation and to generate synthetic or false memory. However, gain-of-function study manipulating CA3 cell ensembles has not been reported. The CA3 area of the hippocampus comprises a recurrent excitatory circuit, which is thought to be important for the generation of associations among the stored information within one brain region. We investigated whether the coincident firing of cell ensembles in one brain region, hippocampal CA3, associates distinct events. CA3 cell ensembles responding to context exploration and during contextual fear conditioning were labeled with channelrhodopsin-2 (ChR2)-mCherry. The synchronous activation of these ensembles induced freezing behavior in mice in a neutral context, in which a foot shock had never been delivered. The recall of this artificial associative fear memory was context specific. In vivo electrophysiological recordings showed that 20-Hz optical stimulation of ChR2-mCherry-expressing CA3 neurons, which is the same stimulation protocol used in behavioral experiment, induced long-term potentiation at CA3-CA3 synapses. Altogether, these results demonstrate that the synchronous activation of ensembles in one brain region, CA3 of the hippocampus, is sufficient for the association of distinct events. The results of our electrophysiology potentially suggest that this artificial association of memory events might be induced by the strengthening of synaptic efficacy between CA3 ensembles via recurrent circuit. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13041-018-0424-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-63237792019-01-11 Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles Oishi, Naoya Nomoto, Masanori Ohkawa, Noriaki Saitoh, Yoshito Sano, Yoshitake Tsujimura, Shuhei Nishizono, Hirofumi Matsuo, Mina Muramatsu, Shin-ichi Inokuchi, Kaoru Mol Brain Research Previous gain-of-function studies using an optogenetic technique showed that manipulation of the hippocampal dentate gyrus or CA1 cell ensembles is important for memory reactivation and to generate synthetic or false memory. However, gain-of-function study manipulating CA3 cell ensembles has not been reported. The CA3 area of the hippocampus comprises a recurrent excitatory circuit, which is thought to be important for the generation of associations among the stored information within one brain region. We investigated whether the coincident firing of cell ensembles in one brain region, hippocampal CA3, associates distinct events. CA3 cell ensembles responding to context exploration and during contextual fear conditioning were labeled with channelrhodopsin-2 (ChR2)-mCherry. The synchronous activation of these ensembles induced freezing behavior in mice in a neutral context, in which a foot shock had never been delivered. The recall of this artificial associative fear memory was context specific. In vivo electrophysiological recordings showed that 20-Hz optical stimulation of ChR2-mCherry-expressing CA3 neurons, which is the same stimulation protocol used in behavioral experiment, induced long-term potentiation at CA3-CA3 synapses. Altogether, these results demonstrate that the synchronous activation of ensembles in one brain region, CA3 of the hippocampus, is sufficient for the association of distinct events. The results of our electrophysiology potentially suggest that this artificial association of memory events might be induced by the strengthening of synaptic efficacy between CA3 ensembles via recurrent circuit. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13041-018-0424-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-08 /pmc/articles/PMC6323779/ /pubmed/30621738 http://dx.doi.org/10.1186/s13041-018-0424-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Oishi, Naoya
Nomoto, Masanori
Ohkawa, Noriaki
Saitoh, Yoshito
Sano, Yoshitake
Tsujimura, Shuhei
Nishizono, Hirofumi
Matsuo, Mina
Muramatsu, Shin-ichi
Inokuchi, Kaoru
Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title_full Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title_fullStr Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title_full_unstemmed Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title_short Artificial association of memory events by optogenetic stimulation of hippocampal CA3 cell ensembles
title_sort artificial association of memory events by optogenetic stimulation of hippocampal ca3 cell ensembles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323779/
https://www.ncbi.nlm.nih.gov/pubmed/30621738
http://dx.doi.org/10.1186/s13041-018-0424-1
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