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Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams
The organization of fear memory involves the participation of multiple brain regions. However, it is largely unknown how fear memory is formed, which circuit pathways are used for “printing” memory engrams across brain regions, and the role of identified brain circuits in memory retrieval. With adva...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590821/ https://www.ncbi.nlm.nih.gov/pubmed/37876798 http://dx.doi.org/10.1016/j.isci.2023.108050 |
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author | Bertocchi, Ilaria Rocha-Almeida, Florbela Romero-Barragán, María Teresa Cambiaghi, Marco Carretero-Guillén, Alejandro Botta, Paolo Dogbevia, Godwin K. Treviño, Mario Mele, Paolo Oberto, Alessandra Larkum, Matthew E. Gruart, Agnes Sprengel, Rolf Delgado-García, José Maria Hasan, Mazahir T. |
author_facet | Bertocchi, Ilaria Rocha-Almeida, Florbela Romero-Barragán, María Teresa Cambiaghi, Marco Carretero-Guillén, Alejandro Botta, Paolo Dogbevia, Godwin K. Treviño, Mario Mele, Paolo Oberto, Alessandra Larkum, Matthew E. Gruart, Agnes Sprengel, Rolf Delgado-García, José Maria Hasan, Mazahir T. |
author_sort | Bertocchi, Ilaria |
collection | PubMed |
description | The organization of fear memory involves the participation of multiple brain regions. However, it is largely unknown how fear memory is formed, which circuit pathways are used for “printing” memory engrams across brain regions, and the role of identified brain circuits in memory retrieval. With advanced genetic methods, we combinatorially blocked presynaptic output and manipulated N-methyl-D-aspartate receptor (NMDAR) in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC) before and after cued fear conditioning. Further, we tagged fear-activated neurons during associative learning for optogenetic memory recall. We found that presynaptic mPFC and postsynaptic BLA NMDARs are required for fear memory formation, but not expression. Our results provide strong evidence that NMDAR-dependent synaptic plasticity drives multi-trace systems consolidation for the sequential printing of fear memory engrams from BLA to mPFC and, subsequently, to the other regions, for flexible memory retrieval. |
format | Online Article Text |
id | pubmed-10590821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105908212023-10-24 Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams Bertocchi, Ilaria Rocha-Almeida, Florbela Romero-Barragán, María Teresa Cambiaghi, Marco Carretero-Guillén, Alejandro Botta, Paolo Dogbevia, Godwin K. Treviño, Mario Mele, Paolo Oberto, Alessandra Larkum, Matthew E. Gruart, Agnes Sprengel, Rolf Delgado-García, José Maria Hasan, Mazahir T. iScience Article The organization of fear memory involves the participation of multiple brain regions. However, it is largely unknown how fear memory is formed, which circuit pathways are used for “printing” memory engrams across brain regions, and the role of identified brain circuits in memory retrieval. With advanced genetic methods, we combinatorially blocked presynaptic output and manipulated N-methyl-D-aspartate receptor (NMDAR) in the basolateral amygdala (BLA) and medial prefrontal cortex (mPFC) before and after cued fear conditioning. Further, we tagged fear-activated neurons during associative learning for optogenetic memory recall. We found that presynaptic mPFC and postsynaptic BLA NMDARs are required for fear memory formation, but not expression. Our results provide strong evidence that NMDAR-dependent synaptic plasticity drives multi-trace systems consolidation for the sequential printing of fear memory engrams from BLA to mPFC and, subsequently, to the other regions, for flexible memory retrieval. Elsevier 2023-09-25 /pmc/articles/PMC10590821/ /pubmed/37876798 http://dx.doi.org/10.1016/j.isci.2023.108050 Text en © 2023. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Bertocchi, Ilaria Rocha-Almeida, Florbela Romero-Barragán, María Teresa Cambiaghi, Marco Carretero-Guillén, Alejandro Botta, Paolo Dogbevia, Godwin K. Treviño, Mario Mele, Paolo Oberto, Alessandra Larkum, Matthew E. Gruart, Agnes Sprengel, Rolf Delgado-García, José Maria Hasan, Mazahir T. Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title | Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title_full | Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title_fullStr | Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title_full_unstemmed | Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title_short | Pre- and postsynaptic N-methyl-D-aspartate receptors are required for sequential printing of fear memory engrams |
title_sort | pre- and postsynaptic n-methyl-d-aspartate receptors are required for sequential printing of fear memory engrams |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590821/ https://www.ncbi.nlm.nih.gov/pubmed/37876798 http://dx.doi.org/10.1016/j.isci.2023.108050 |
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