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Synaptic plasticity-dependent competition rule influences memory formation
Memory is supported by a specific collection of neurons distributed in broad brain areas, an engram. Despite recent advances in identifying an engram, how the engram is created during memory formation remains elusive. To explore the relation between a specific pattern of input activity and memory al...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225794/ https://www.ncbi.nlm.nih.gov/pubmed/34168140 http://dx.doi.org/10.1038/s41467-021-24269-4 |
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author | Jeong, Yire Cho, Hye-Yeon Kim, Mujun Oh, Jung-Pyo Kang, Min Soo Yoo, Miran Lee, Han-Sol Han, Jin-Hee |
author_facet | Jeong, Yire Cho, Hye-Yeon Kim, Mujun Oh, Jung-Pyo Kang, Min Soo Yoo, Miran Lee, Han-Sol Han, Jin-Hee |
author_sort | Jeong, Yire |
collection | PubMed |
description | Memory is supported by a specific collection of neurons distributed in broad brain areas, an engram. Despite recent advances in identifying an engram, how the engram is created during memory formation remains elusive. To explore the relation between a specific pattern of input activity and memory allocation, here we target a sparse subset of neurons in the auditory cortex and thalamus. The synaptic inputs from these neurons to the lateral amygdala (LA) are not potentiated by fear conditioning. Using an optogenetic priming stimulus, we manipulate these synapses to be potentiated by the learning. In this condition, fear memory is preferentially encoded in the manipulated cell ensembles. This change, however, is abolished with optical long-term depression (LTD) delivered shortly after training. Conversely, delivering optical long-term potentiation (LTP) alone shortly after fear conditioning is sufficient to induce the preferential memory encoding. These results suggest a synaptic plasticity-dependent competition rule underlying memory formation. |
format | Online Article Text |
id | pubmed-8225794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82257942021-07-09 Synaptic plasticity-dependent competition rule influences memory formation Jeong, Yire Cho, Hye-Yeon Kim, Mujun Oh, Jung-Pyo Kang, Min Soo Yoo, Miran Lee, Han-Sol Han, Jin-Hee Nat Commun Article Memory is supported by a specific collection of neurons distributed in broad brain areas, an engram. Despite recent advances in identifying an engram, how the engram is created during memory formation remains elusive. To explore the relation between a specific pattern of input activity and memory allocation, here we target a sparse subset of neurons in the auditory cortex and thalamus. The synaptic inputs from these neurons to the lateral amygdala (LA) are not potentiated by fear conditioning. Using an optogenetic priming stimulus, we manipulate these synapses to be potentiated by the learning. In this condition, fear memory is preferentially encoded in the manipulated cell ensembles. This change, however, is abolished with optical long-term depression (LTD) delivered shortly after training. Conversely, delivering optical long-term potentiation (LTP) alone shortly after fear conditioning is sufficient to induce the preferential memory encoding. These results suggest a synaptic plasticity-dependent competition rule underlying memory formation. Nature Publishing Group UK 2021-06-24 /pmc/articles/PMC8225794/ /pubmed/34168140 http://dx.doi.org/10.1038/s41467-021-24269-4 Text en © The Author(s) 2021 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 Jeong, Yire Cho, Hye-Yeon Kim, Mujun Oh, Jung-Pyo Kang, Min Soo Yoo, Miran Lee, Han-Sol Han, Jin-Hee Synaptic plasticity-dependent competition rule influences memory formation |
title | Synaptic plasticity-dependent competition rule influences memory formation |
title_full | Synaptic plasticity-dependent competition rule influences memory formation |
title_fullStr | Synaptic plasticity-dependent competition rule influences memory formation |
title_full_unstemmed | Synaptic plasticity-dependent competition rule influences memory formation |
title_short | Synaptic plasticity-dependent competition rule influences memory formation |
title_sort | synaptic plasticity-dependent competition rule influences memory formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225794/ https://www.ncbi.nlm.nih.gov/pubmed/34168140 http://dx.doi.org/10.1038/s41467-021-24269-4 |
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