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Engram Size Varies with Learning and Reflects Memory Content and Precision

Memories are rarely acquired under ideal conditions, rendering them vulnerable to profound omissions, errors, and ambiguities. Consistent with this, recent work using context fear conditioning has shown that memories formed after inadequate learning time display a variety of maladaptive properties,...

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Autores principales: Leake, Jessica, Zinn, Raphael, Corbit, Laura H., Fanselow, Michael S., Vissel, Bryce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176757/
https://www.ncbi.nlm.nih.gov/pubmed/33888604
http://dx.doi.org/10.1523/JNEUROSCI.2786-20.2021
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author Leake, Jessica
Zinn, Raphael
Corbit, Laura H.
Fanselow, Michael S.
Vissel, Bryce
author_facet Leake, Jessica
Zinn, Raphael
Corbit, Laura H.
Fanselow, Michael S.
Vissel, Bryce
author_sort Leake, Jessica
collection PubMed
description Memories are rarely acquired under ideal conditions, rendering them vulnerable to profound omissions, errors, and ambiguities. Consistent with this, recent work using context fear conditioning has shown that memories formed after inadequate learning time display a variety of maladaptive properties, including overgeneralization to similar contexts. However, the neuronal basis of such poor learning and memory imprecision remains unknown. Using c-fos to track neuronal activity in male mice, we examined how these learning-dependent changes in context fear memory precision are encoded in hippocampal ensembles. We found that the total number of c-fos-encoding cells did not correspond with learning history but instead more closely reflected the length of the session immediately preceding c-fos measurement. However, using a c-fos-driven tagging method (TRAP2 mouse line), we found that the degree of learning and memory specificity corresponded with neuronal activity in a subset of dentate gyrus cells that were active during both learning and recall. Comprehensive memories acquired after longer learning intervals were associated with more double-labeled cells. These were preferentially reactivated in the conditioning context compared with a similar context, paralleling behavioral discrimination. Conversely, impoverished memories acquired after shorter learning intervals were associated with fewer double-labeled cells. These were reactivated equally in both contexts, corresponding with overgeneralization. Together, these findings provide two surprising conclusions. First, engram size varies with learning. Second, larger engrams support better neuronal and behavioral discrimination. These findings are incorporated into a model that describes how neuronal activity is influenced by previous learning and present experience, thus driving behavior. SIGNIFICANCE STATEMENT Memories are not always formed under ideal circumstances. This is especially true in traumatic situations, such as car accidents, where individuals have insufficient time to process what happened around them. Such memories have the potential to overgeneralize to irrelevant situations, producing inappropriate fear and contributing to disorders, such as post-traumatic stress disorder. However, it is unknown how such poorly formed fear memories are encoded within the brain. We find that restricting learning time results in fear memories that are encoded by fewer hippocampal cells. Moreover, these fewer cells are inappropriately reactivated in both dangerous and safe contexts. These findings suggest that fear memories formed at brief periods overgeneralize because they lack the detail-rich information necessary to support neuronal discrimination.
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spelling pubmed-81767572021-06-04 Engram Size Varies with Learning and Reflects Memory Content and Precision Leake, Jessica Zinn, Raphael Corbit, Laura H. Fanselow, Michael S. Vissel, Bryce J Neurosci Research Articles Memories are rarely acquired under ideal conditions, rendering them vulnerable to profound omissions, errors, and ambiguities. Consistent with this, recent work using context fear conditioning has shown that memories formed after inadequate learning time display a variety of maladaptive properties, including overgeneralization to similar contexts. However, the neuronal basis of such poor learning and memory imprecision remains unknown. Using c-fos to track neuronal activity in male mice, we examined how these learning-dependent changes in context fear memory precision are encoded in hippocampal ensembles. We found that the total number of c-fos-encoding cells did not correspond with learning history but instead more closely reflected the length of the session immediately preceding c-fos measurement. However, using a c-fos-driven tagging method (TRAP2 mouse line), we found that the degree of learning and memory specificity corresponded with neuronal activity in a subset of dentate gyrus cells that were active during both learning and recall. Comprehensive memories acquired after longer learning intervals were associated with more double-labeled cells. These were preferentially reactivated in the conditioning context compared with a similar context, paralleling behavioral discrimination. Conversely, impoverished memories acquired after shorter learning intervals were associated with fewer double-labeled cells. These were reactivated equally in both contexts, corresponding with overgeneralization. Together, these findings provide two surprising conclusions. First, engram size varies with learning. Second, larger engrams support better neuronal and behavioral discrimination. These findings are incorporated into a model that describes how neuronal activity is influenced by previous learning and present experience, thus driving behavior. SIGNIFICANCE STATEMENT Memories are not always formed under ideal circumstances. This is especially true in traumatic situations, such as car accidents, where individuals have insufficient time to process what happened around them. Such memories have the potential to overgeneralize to irrelevant situations, producing inappropriate fear and contributing to disorders, such as post-traumatic stress disorder. However, it is unknown how such poorly formed fear memories are encoded within the brain. We find that restricting learning time results in fear memories that are encoded by fewer hippocampal cells. Moreover, these fewer cells are inappropriately reactivated in both dangerous and safe contexts. These findings suggest that fear memories formed at brief periods overgeneralize because they lack the detail-rich information necessary to support neuronal discrimination. Society for Neuroscience 2021-05-05 /pmc/articles/PMC8176757/ /pubmed/33888604 http://dx.doi.org/10.1523/JNEUROSCI.2786-20.2021 Text en Copyright © 2021 Leake, Zinn et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Articles
Leake, Jessica
Zinn, Raphael
Corbit, Laura H.
Fanselow, Michael S.
Vissel, Bryce
Engram Size Varies with Learning and Reflects Memory Content and Precision
title Engram Size Varies with Learning and Reflects Memory Content and Precision
title_full Engram Size Varies with Learning and Reflects Memory Content and Precision
title_fullStr Engram Size Varies with Learning and Reflects Memory Content and Precision
title_full_unstemmed Engram Size Varies with Learning and Reflects Memory Content and Precision
title_short Engram Size Varies with Learning and Reflects Memory Content and Precision
title_sort engram size varies with learning and reflects memory content and precision
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8176757/
https://www.ncbi.nlm.nih.gov/pubmed/33888604
http://dx.doi.org/10.1523/JNEUROSCI.2786-20.2021
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