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Dynamic frontotemporal systems process space and time in working memory

How do we rapidly process incoming streams of information in working memory, a cognitive mechanism central to human behavior? Dominant views of working memory focus on the prefrontal cortex (PFC), but human hippocampal recordings provide a neurophysiological signature distinct from the PFC. Are thes...

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Autores principales: Johnson, Elizabeth L., Adams, Jenna N., Solbakk, Anne-Kristin, Endestad, Tor, Larsson, Pål G., Ivanovic, Jugoslav, Meling, Torstein R., Lin, Jack J., Knight, Robert T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895055/
https://www.ncbi.nlm.nih.gov/pubmed/29601574
http://dx.doi.org/10.1371/journal.pbio.2004274
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author Johnson, Elizabeth L.
Adams, Jenna N.
Solbakk, Anne-Kristin
Endestad, Tor
Larsson, Pål G.
Ivanovic, Jugoslav
Meling, Torstein R.
Lin, Jack J.
Knight, Robert T.
author_facet Johnson, Elizabeth L.
Adams, Jenna N.
Solbakk, Anne-Kristin
Endestad, Tor
Larsson, Pål G.
Ivanovic, Jugoslav
Meling, Torstein R.
Lin, Jack J.
Knight, Robert T.
author_sort Johnson, Elizabeth L.
collection PubMed
description How do we rapidly process incoming streams of information in working memory, a cognitive mechanism central to human behavior? Dominant views of working memory focus on the prefrontal cortex (PFC), but human hippocampal recordings provide a neurophysiological signature distinct from the PFC. Are these regions independent, or do they interact in the service of working memory? We addressed this core issue in behavior by recording directly from frontotemporal sites in humans performing a visuospatial working memory task that operationalizes the types of identity and spatiotemporal information we encounter every day. Theta band oscillations drove bidirectional interactions between the PFC and medial temporal lobe (MTL; including the hippocampus). MTL theta oscillations directed the PFC preferentially during the processing of spatiotemporal information, while PFC theta oscillations directed the MTL for all types of information being processed in working memory. These findings reveal an MTL theta mechanism for processing space and time and a domain-general PFC theta mechanism, providing evidence that rapid, dynamic MTL–PFC interactions underlie working memory for everyday experiences.
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spelling pubmed-58950552018-05-04 Dynamic frontotemporal systems process space and time in working memory Johnson, Elizabeth L. Adams, Jenna N. Solbakk, Anne-Kristin Endestad, Tor Larsson, Pål G. Ivanovic, Jugoslav Meling, Torstein R. Lin, Jack J. Knight, Robert T. PLoS Biol Research Article How do we rapidly process incoming streams of information in working memory, a cognitive mechanism central to human behavior? Dominant views of working memory focus on the prefrontal cortex (PFC), but human hippocampal recordings provide a neurophysiological signature distinct from the PFC. Are these regions independent, or do they interact in the service of working memory? We addressed this core issue in behavior by recording directly from frontotemporal sites in humans performing a visuospatial working memory task that operationalizes the types of identity and spatiotemporal information we encounter every day. Theta band oscillations drove bidirectional interactions between the PFC and medial temporal lobe (MTL; including the hippocampus). MTL theta oscillations directed the PFC preferentially during the processing of spatiotemporal information, while PFC theta oscillations directed the MTL for all types of information being processed in working memory. These findings reveal an MTL theta mechanism for processing space and time and a domain-general PFC theta mechanism, providing evidence that rapid, dynamic MTL–PFC interactions underlie working memory for everyday experiences. Public Library of Science 2018-03-30 /pmc/articles/PMC5895055/ /pubmed/29601574 http://dx.doi.org/10.1371/journal.pbio.2004274 Text en © 2018 Johnson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Johnson, Elizabeth L.
Adams, Jenna N.
Solbakk, Anne-Kristin
Endestad, Tor
Larsson, Pål G.
Ivanovic, Jugoslav
Meling, Torstein R.
Lin, Jack J.
Knight, Robert T.
Dynamic frontotemporal systems process space and time in working memory
title Dynamic frontotemporal systems process space and time in working memory
title_full Dynamic frontotemporal systems process space and time in working memory
title_fullStr Dynamic frontotemporal systems process space and time in working memory
title_full_unstemmed Dynamic frontotemporal systems process space and time in working memory
title_short Dynamic frontotemporal systems process space and time in working memory
title_sort dynamic frontotemporal systems process space and time in working memory
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895055/
https://www.ncbi.nlm.nih.gov/pubmed/29601574
http://dx.doi.org/10.1371/journal.pbio.2004274
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