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Entorhinal cortex directs learning-related changes in CA1 representations
Learning-related changes in brain activity are thought to underlie adaptive behaviours(1,2). For instance, the learning of a reward site by rodents requires the development of an over-representation of that location in the hippocampus(3–6). How this learning-related change occurs remains unknown. He...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668747/ https://www.ncbi.nlm.nih.gov/pubmed/36323779 http://dx.doi.org/10.1038/s41586-022-05378-6 |
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author | Grienberger, Christine Magee, Jeffrey C. |
author_facet | Grienberger, Christine Magee, Jeffrey C. |
author_sort | Grienberger, Christine |
collection | PubMed |
description | Learning-related changes in brain activity are thought to underlie adaptive behaviours(1,2). For instance, the learning of a reward site by rodents requires the development of an over-representation of that location in the hippocampus(3–6). How this learning-related change occurs remains unknown. Here we recorded hippocampal CA1 population activity as mice learned a reward location on a linear treadmill. Physiological and pharmacological evidence suggests that the adaptive over-representation required behavioural timescale synaptic plasticity (BTSP)(7). BTSP is known to be driven by dendritic voltage signals that we proposed were initiated by input from entorhinal cortex layer 3 (EC3). Accordingly, the CA1 over-representation was largely removed by optogenetic inhibition of EC3 activity. Recordings from EC3 neurons revealed an activity pattern that could provide an instructive signal directing BTSP to generate the over-representation. Consistent with this function, our observations show that exposure to a second environment possessing a prominent reward-predictive cue resulted in both EC3 activity and CA1 place field density that were more elevated at the cue than at the reward. These data indicate that learning-related changes in the hippocampus are produced by synaptic plasticity directed by an instructive signal from the EC3 that seems to be specifically adapted to the behaviourally relevant features of the environment. |
format | Online Article Text |
id | pubmed-9668747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96687472022-11-18 Entorhinal cortex directs learning-related changes in CA1 representations Grienberger, Christine Magee, Jeffrey C. Nature Article Learning-related changes in brain activity are thought to underlie adaptive behaviours(1,2). For instance, the learning of a reward site by rodents requires the development of an over-representation of that location in the hippocampus(3–6). How this learning-related change occurs remains unknown. Here we recorded hippocampal CA1 population activity as mice learned a reward location on a linear treadmill. Physiological and pharmacological evidence suggests that the adaptive over-representation required behavioural timescale synaptic plasticity (BTSP)(7). BTSP is known to be driven by dendritic voltage signals that we proposed were initiated by input from entorhinal cortex layer 3 (EC3). Accordingly, the CA1 over-representation was largely removed by optogenetic inhibition of EC3 activity. Recordings from EC3 neurons revealed an activity pattern that could provide an instructive signal directing BTSP to generate the over-representation. Consistent with this function, our observations show that exposure to a second environment possessing a prominent reward-predictive cue resulted in both EC3 activity and CA1 place field density that were more elevated at the cue than at the reward. These data indicate that learning-related changes in the hippocampus are produced by synaptic plasticity directed by an instructive signal from the EC3 that seems to be specifically adapted to the behaviourally relevant features of the environment. Nature Publishing Group UK 2022-11-02 2022 /pmc/articles/PMC9668747/ /pubmed/36323779 http://dx.doi.org/10.1038/s41586-022-05378-6 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Grienberger, Christine Magee, Jeffrey C. Entorhinal cortex directs learning-related changes in CA1 representations |
title | Entorhinal cortex directs learning-related changes in CA1 representations |
title_full | Entorhinal cortex directs learning-related changes in CA1 representations |
title_fullStr | Entorhinal cortex directs learning-related changes in CA1 representations |
title_full_unstemmed | Entorhinal cortex directs learning-related changes in CA1 representations |
title_short | Entorhinal cortex directs learning-related changes in CA1 representations |
title_sort | entorhinal cortex directs learning-related changes in ca1 representations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668747/ https://www.ncbi.nlm.nih.gov/pubmed/36323779 http://dx.doi.org/10.1038/s41586-022-05378-6 |
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