Cargando…
Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice
Observers learn to fear the context in which they witnessed a demonstrator’s aversive experience, called observational contextual fear conditioning (CFC). The neural mechanisms governing whether recall of the observational CFC memory occurs from the observer’s own or from the demonstrator’s point of...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322999/ https://www.ncbi.nlm.nih.gov/pubmed/37407567 http://dx.doi.org/10.1038/s41467-023-39718-5 |
_version_ | 1785068881992220672 |
---|---|
author | Terranova, Joseph I. Yokose, Jun Osanai, Hisayuki Ogawa, Sachie K. Kitamura, Takashi |
author_facet | Terranova, Joseph I. Yokose, Jun Osanai, Hisayuki Ogawa, Sachie K. Kitamura, Takashi |
author_sort | Terranova, Joseph I. |
collection | PubMed |
description | Observers learn to fear the context in which they witnessed a demonstrator’s aversive experience, called observational contextual fear conditioning (CFC). The neural mechanisms governing whether recall of the observational CFC memory occurs from the observer’s own or from the demonstrator’s point of view remain unclear. Here, we show in male mice that recent observational CFC memory is recalled in the observer’s context only, but remote memory is recalled in both observer and demonstrator contexts. Recall of recent memory in the observer’s context requires dorsal hippocampus activity, while recall of remote memory in both contexts requires the medial prefrontal cortex (mPFC)-basolateral amygdala pathway. Although mPFC neurons activated by observational CFC are involved in remote recall in both contexts, distinct mPFC subpopulations regulate remote recall in each context. Our data provide insights into a flexible recall strategy and the functional reorganization of circuits and memory engram cells underlying observational CFC memory. |
format | Online Article Text |
id | pubmed-10322999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103229992023-07-07 Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice Terranova, Joseph I. Yokose, Jun Osanai, Hisayuki Ogawa, Sachie K. Kitamura, Takashi Nat Commun Article Observers learn to fear the context in which they witnessed a demonstrator’s aversive experience, called observational contextual fear conditioning (CFC). The neural mechanisms governing whether recall of the observational CFC memory occurs from the observer’s own or from the demonstrator’s point of view remain unclear. Here, we show in male mice that recent observational CFC memory is recalled in the observer’s context only, but remote memory is recalled in both observer and demonstrator contexts. Recall of recent memory in the observer’s context requires dorsal hippocampus activity, while recall of remote memory in both contexts requires the medial prefrontal cortex (mPFC)-basolateral amygdala pathway. Although mPFC neurons activated by observational CFC are involved in remote recall in both contexts, distinct mPFC subpopulations regulate remote recall in each context. Our data provide insights into a flexible recall strategy and the functional reorganization of circuits and memory engram cells underlying observational CFC memory. Nature Publishing Group UK 2023-07-05 /pmc/articles/PMC10322999/ /pubmed/37407567 http://dx.doi.org/10.1038/s41467-023-39718-5 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 Terranova, Joseph I. Yokose, Jun Osanai, Hisayuki Ogawa, Sachie K. Kitamura, Takashi Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title | Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title_full | Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title_fullStr | Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title_full_unstemmed | Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title_short | Systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
title_sort | systems consolidation induces multiple memory engrams for a flexible recall strategy in observational fear memory in male mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322999/ https://www.ncbi.nlm.nih.gov/pubmed/37407567 http://dx.doi.org/10.1038/s41467-023-39718-5 |
work_keys_str_mv | AT terranovajosephi systemsconsolidationinducesmultiplememoryengramsforaflexiblerecallstrategyinobservationalfearmemoryinmalemice AT yokosejun systemsconsolidationinducesmultiplememoryengramsforaflexiblerecallstrategyinobservationalfearmemoryinmalemice AT osanaihisayuki systemsconsolidationinducesmultiplememoryengramsforaflexiblerecallstrategyinobservationalfearmemoryinmalemice AT ogawasachiek systemsconsolidationinducesmultiplememoryengramsforaflexiblerecallstrategyinobservationalfearmemoryinmalemice AT kitamuratakashi systemsconsolidationinducesmultiplememoryengramsforaflexiblerecallstrategyinobservationalfearmemoryinmalemice |