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Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events
We remember our lives as sequences of events, but it is unclear how these memories are controlled during retrieval. In rats, the medial prefrontal cortex (mPFC) is positioned to influence sequence memory through extensive top-down inputs to regions heavily interconnected with the hippocampus, notabl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662648/ https://www.ncbi.nlm.nih.gov/pubmed/31315044 http://dx.doi.org/10.1016/j.celrep.2019.06.053 |
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author | Jayachandran, Maanasa Linley, Stephanie B. Schlecht, Maximilian Mahler, Stephen V. Vertes, Robert P. Allen, Timothy A. |
author_facet | Jayachandran, Maanasa Linley, Stephanie B. Schlecht, Maximilian Mahler, Stephen V. Vertes, Robert P. Allen, Timothy A. |
author_sort | Jayachandran, Maanasa |
collection | PubMed |
description | We remember our lives as sequences of events, but it is unclear how these memories are controlled during retrieval. In rats, the medial prefrontal cortex (mPFC) is positioned to influence sequence memory through extensive top-down inputs to regions heavily interconnected with the hippocampus, notably the nucleus reuniens of the thalamus (RE) and perirhinal cortex (PER). Here, we used an hM4Di synaptic-silencing approach to test our hypothesis that specific mPFC→RE and mPFC→PER projections regulate sequence memory retrieval. First, we found non-overlapping populations of mPFC cells project to RE and PER. Second, suppressing mPFC activity impaired sequence memory. Third, inhibiting mPFC→RE and mPFC→PER pathways effectively abolished sequence memory. Finally, a sequential lag analysis showed that the mPFC→RE pathway contributes to a working memory retrieval strategy, whereas the mPFC→PER pathway supports a temporal context memory retrieval strategy. These findings demonstrate that mPFC→RE and mPFC→PER pathways serve as top-down mechanisms that control distinct sequence memory retrieval strategies. |
format | Online Article Text |
id | pubmed-6662648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-66626482019-07-29 Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events Jayachandran, Maanasa Linley, Stephanie B. Schlecht, Maximilian Mahler, Stephen V. Vertes, Robert P. Allen, Timothy A. Cell Rep Article We remember our lives as sequences of events, but it is unclear how these memories are controlled during retrieval. In rats, the medial prefrontal cortex (mPFC) is positioned to influence sequence memory through extensive top-down inputs to regions heavily interconnected with the hippocampus, notably the nucleus reuniens of the thalamus (RE) and perirhinal cortex (PER). Here, we used an hM4Di synaptic-silencing approach to test our hypothesis that specific mPFC→RE and mPFC→PER projections regulate sequence memory retrieval. First, we found non-overlapping populations of mPFC cells project to RE and PER. Second, suppressing mPFC activity impaired sequence memory. Third, inhibiting mPFC→RE and mPFC→PER pathways effectively abolished sequence memory. Finally, a sequential lag analysis showed that the mPFC→RE pathway contributes to a working memory retrieval strategy, whereas the mPFC→PER pathway supports a temporal context memory retrieval strategy. These findings demonstrate that mPFC→RE and mPFC→PER pathways serve as top-down mechanisms that control distinct sequence memory retrieval strategies. 2019-07-16 /pmc/articles/PMC6662648/ /pubmed/31315044 http://dx.doi.org/10.1016/j.celrep.2019.06.053 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Jayachandran, Maanasa Linley, Stephanie B. Schlecht, Maximilian Mahler, Stephen V. Vertes, Robert P. Allen, Timothy A. Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title | Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title_full | Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title_fullStr | Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title_full_unstemmed | Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title_short | Prefrontal Pathways Provide Top-Down Control of Memory for Sequences of Events |
title_sort | prefrontal pathways provide top-down control of memory for sequences of events |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662648/ https://www.ncbi.nlm.nih.gov/pubmed/31315044 http://dx.doi.org/10.1016/j.celrep.2019.06.053 |
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