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The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity

Brain states such as arousal and sleep play critical roles in memory encoding, storage, and recall. Recent studies have highlighted the role of engram neurons–populations of neurons activated during learning–in subsequent memory consolidation and recall. These engram populations are generally assume...

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Autores principales: Raven, Frank, Aton, Sara J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473837/
https://www.ncbi.nlm.nih.gov/pubmed/34588960
http://dx.doi.org/10.3389/fncir.2021.750541
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author Raven, Frank
Aton, Sara J.
author_facet Raven, Frank
Aton, Sara J.
author_sort Raven, Frank
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description Brain states such as arousal and sleep play critical roles in memory encoding, storage, and recall. Recent studies have highlighted the role of engram neurons–populations of neurons activated during learning–in subsequent memory consolidation and recall. These engram populations are generally assumed to be glutamatergic, and the vast majority of data regarding the function of engram neurons have focused on glutamatergic pyramidal or granule cell populations in either the hippocampus, amygdala, or neocortex. Recent data suggest that sleep and wake states differentially regulate the activity and temporal dynamics of engram neurons. Two potential mechanisms for this regulation are either via direct regulation of glutamatergic engram neuron excitability and firing, or via state-dependent effects on interneuron populations–which in turn modulate the activity of glutamatergic engram neurons. Here, we will discuss recent findings related to the roles of interneurons in state-regulated memory processes and synaptic plasticity, and the potential therapeutic implications of understanding these mechanisms.
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spelling pubmed-84738372021-09-28 The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity Raven, Frank Aton, Sara J. Front Neural Circuits Neural Circuits Brain states such as arousal and sleep play critical roles in memory encoding, storage, and recall. Recent studies have highlighted the role of engram neurons–populations of neurons activated during learning–in subsequent memory consolidation and recall. These engram populations are generally assumed to be glutamatergic, and the vast majority of data regarding the function of engram neurons have focused on glutamatergic pyramidal or granule cell populations in either the hippocampus, amygdala, or neocortex. Recent data suggest that sleep and wake states differentially regulate the activity and temporal dynamics of engram neurons. Two potential mechanisms for this regulation are either via direct regulation of glutamatergic engram neuron excitability and firing, or via state-dependent effects on interneuron populations–which in turn modulate the activity of glutamatergic engram neurons. Here, we will discuss recent findings related to the roles of interneurons in state-regulated memory processes and synaptic plasticity, and the potential therapeutic implications of understanding these mechanisms. Frontiers Media S.A. 2021-09-13 /pmc/articles/PMC8473837/ /pubmed/34588960 http://dx.doi.org/10.3389/fncir.2021.750541 Text en Copyright © 2021 Raven and Aton. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neural Circuits
Raven, Frank
Aton, Sara J.
The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title_full The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title_fullStr The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title_full_unstemmed The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title_short The Engram’s Dark Horse: How Interneurons Regulate State-Dependent Memory Processing and Plasticity
title_sort engram’s dark horse: how interneurons regulate state-dependent memory processing and plasticity
topic Neural Circuits
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473837/
https://www.ncbi.nlm.nih.gov/pubmed/34588960
http://dx.doi.org/10.3389/fncir.2021.750541
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