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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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