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Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales

Converging, cross-species evidence indicates that memory for time is supported by hippocampal area CA1 and entorhinal cortex. However, limited evidence characterizes how these regions preserve temporal memories over long timescales (e.g., months). At long timescales, memoranda may be encountered in...

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Autores principales: Zou, Futing, Wanjia, Guo, Allen, Emily J., Wu, Yihan, Charest, Ian, Naselaris, Thomas, Kay, Kendrick, Kuhl, Brice A., Hutchinson, J. Benjamin, DuBrow, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356845/
https://www.ncbi.nlm.nih.gov/pubmed/37468489
http://dx.doi.org/10.1038/s41467-023-40100-8
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author Zou, Futing
Wanjia, Guo
Allen, Emily J.
Wu, Yihan
Charest, Ian
Naselaris, Thomas
Kay, Kendrick
Kuhl, Brice A.
Hutchinson, J. Benjamin
DuBrow, Sarah
author_facet Zou, Futing
Wanjia, Guo
Allen, Emily J.
Wu, Yihan
Charest, Ian
Naselaris, Thomas
Kay, Kendrick
Kuhl, Brice A.
Hutchinson, J. Benjamin
DuBrow, Sarah
author_sort Zou, Futing
collection PubMed
description Converging, cross-species evidence indicates that memory for time is supported by hippocampal area CA1 and entorhinal cortex. However, limited evidence characterizes how these regions preserve temporal memories over long timescales (e.g., months). At long timescales, memoranda may be encountered in multiple temporal contexts, potentially creating interference. Here, using 7T fMRI, we measured CA1 and entorhinal activity patterns as human participants viewed thousands of natural scene images distributed, and repeated, across many months. We show that memory for an image’s original temporal context was predicted by the degree to which CA1/entorhinal activity patterns from the first encounter with an image were re-expressed during re-encounters occurring minutes to months later. Critically, temporal memory signals were dissociable from predictors of recognition confidence, which were carried by distinct medial temporal lobe expressions. These findings suggest that CA1 and entorhinal cortex preserve temporal memories across long timescales by coding for and reinstating temporal context information.
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spelling pubmed-103568452023-07-21 Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales Zou, Futing Wanjia, Guo Allen, Emily J. Wu, Yihan Charest, Ian Naselaris, Thomas Kay, Kendrick Kuhl, Brice A. Hutchinson, J. Benjamin DuBrow, Sarah Nat Commun Article Converging, cross-species evidence indicates that memory for time is supported by hippocampal area CA1 and entorhinal cortex. However, limited evidence characterizes how these regions preserve temporal memories over long timescales (e.g., months). At long timescales, memoranda may be encountered in multiple temporal contexts, potentially creating interference. Here, using 7T fMRI, we measured CA1 and entorhinal activity patterns as human participants viewed thousands of natural scene images distributed, and repeated, across many months. We show that memory for an image’s original temporal context was predicted by the degree to which CA1/entorhinal activity patterns from the first encounter with an image were re-expressed during re-encounters occurring minutes to months later. Critically, temporal memory signals were dissociable from predictors of recognition confidence, which were carried by distinct medial temporal lobe expressions. These findings suggest that CA1 and entorhinal cortex preserve temporal memories across long timescales by coding for and reinstating temporal context information. Nature Publishing Group UK 2023-07-19 /pmc/articles/PMC10356845/ /pubmed/37468489 http://dx.doi.org/10.1038/s41467-023-40100-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zou, Futing
Wanjia, Guo
Allen, Emily J.
Wu, Yihan
Charest, Ian
Naselaris, Thomas
Kay, Kendrick
Kuhl, Brice A.
Hutchinson, J. Benjamin
DuBrow, Sarah
Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title_full Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title_fullStr Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title_full_unstemmed Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title_short Re-expression of CA1 and entorhinal activity patterns preserves temporal context memory at long timescales
title_sort re-expression of ca1 and entorhinal activity patterns preserves temporal context memory at long timescales
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356845/
https://www.ncbi.nlm.nih.gov/pubmed/37468489
http://dx.doi.org/10.1038/s41467-023-40100-8
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