Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jayachandran, Maanasa, Linley, Stephanie B., Schlecht, Maximilian, Mahler, Stephen V., Vertes, Robert P., Allen, Timothy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
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
_version_ 1783439683847454720
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
work_keys_str_mv AT jayachandranmaanasa prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents
AT linleystephanieb prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents
AT schlechtmaximilian prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents
AT mahlerstephenv prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents
AT vertesrobertp prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents
AT allentimothya prefrontalpathwaysprovidetopdowncontrolofmemoryforsequencesofevents