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Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning

It is widely accepted that some types of learning involve structural and functional changes of hippocampal synapses. Cell adhesion molecules neural cell adhesion molecule (NCAM), its polysialylated form polysialic acid to NCAM (PSA-NCAM), and L1 are prominent modulators of those changes. On the othe...

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Autores principales: Navarro-López, Juan D., Contreras, Ana, Touyarot, Katia, Herrero, Ana I., Venero, César, Cambon, Karine, Gruart, Agnés, Delgado-García, José M., Sandi, Carmen, Jiménez-Díaz, Lydia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811386/
https://www.ncbi.nlm.nih.gov/pubmed/36620194
http://dx.doi.org/10.3389/fnana.2022.1082701
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author Navarro-López, Juan D.
Contreras, Ana
Touyarot, Katia
Herrero, Ana I.
Venero, César
Cambon, Karine
Gruart, Agnés
Delgado-García, José M.
Sandi, Carmen
Jiménez-Díaz, Lydia
author_facet Navarro-López, Juan D.
Contreras, Ana
Touyarot, Katia
Herrero, Ana I.
Venero, César
Cambon, Karine
Gruart, Agnés
Delgado-García, José M.
Sandi, Carmen
Jiménez-Díaz, Lydia
author_sort Navarro-López, Juan D.
collection PubMed
description It is widely accepted that some types of learning involve structural and functional changes of hippocampal synapses. Cell adhesion molecules neural cell adhesion molecule (NCAM), its polysialylated form polysialic acid to NCAM (PSA-NCAM), and L1 are prominent modulators of those changes. On the other hand, trace eyeblink conditioning, an associative motor learning task, requires the active participation of hippocampal circuits. However, the involvement of NCAM, PSA-NCAM, and L1 in this type of learning is not fully known. Here, we aimed to investigate the possible time sequence modifications of such neural cell adhesion molecules in the hippocampus during the acquisition of a trace eyeblink conditioning. To do so, the hippocampal expression of NCAM, PSA-NCAM, and L1 was assessed at three different time points during conditioning: after one (initial acquisition), three (partial acquisition), and six (complete acquisition) sessions of the conditioning paradigm. The conditioned stimulus (CS) was a weak electrical pulse separated by a 250-ms time interval from the unconditioned stimuli (US, a strong electrical pulse). An acquisition-dependent regulation of these adhesion molecules was found in the hippocampus. During the initial acquisition of the conditioning eyeblink paradigm (12 h after 1 and 3 days of training), synaptic expression of L1 and PSA-NCAM was transiently increased in the contralateral hippocampus to the paired CS-US presentations, whereas, when the associative learning was completed, such increase disappeared, but a marked and bilateral upregulation of NCAM was found. In conclusion, our findings show a specific temporal pattern of hippocampal CAMs expression during the acquisition process, highlighting the relevance of NCAM, PSA-NCAM, and L1 as learning-modulated molecules critically involved in remodeling processes underlying associative motor-memories formation.
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spelling pubmed-98113862023-01-05 Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning Navarro-López, Juan D. Contreras, Ana Touyarot, Katia Herrero, Ana I. Venero, César Cambon, Karine Gruart, Agnés Delgado-García, José M. Sandi, Carmen Jiménez-Díaz, Lydia Front Neuroanat Neuroanatomy It is widely accepted that some types of learning involve structural and functional changes of hippocampal synapses. Cell adhesion molecules neural cell adhesion molecule (NCAM), its polysialylated form polysialic acid to NCAM (PSA-NCAM), and L1 are prominent modulators of those changes. On the other hand, trace eyeblink conditioning, an associative motor learning task, requires the active participation of hippocampal circuits. However, the involvement of NCAM, PSA-NCAM, and L1 in this type of learning is not fully known. Here, we aimed to investigate the possible time sequence modifications of such neural cell adhesion molecules in the hippocampus during the acquisition of a trace eyeblink conditioning. To do so, the hippocampal expression of NCAM, PSA-NCAM, and L1 was assessed at three different time points during conditioning: after one (initial acquisition), three (partial acquisition), and six (complete acquisition) sessions of the conditioning paradigm. The conditioned stimulus (CS) was a weak electrical pulse separated by a 250-ms time interval from the unconditioned stimuli (US, a strong electrical pulse). An acquisition-dependent regulation of these adhesion molecules was found in the hippocampus. During the initial acquisition of the conditioning eyeblink paradigm (12 h after 1 and 3 days of training), synaptic expression of L1 and PSA-NCAM was transiently increased in the contralateral hippocampus to the paired CS-US presentations, whereas, when the associative learning was completed, such increase disappeared, but a marked and bilateral upregulation of NCAM was found. In conclusion, our findings show a specific temporal pattern of hippocampal CAMs expression during the acquisition process, highlighting the relevance of NCAM, PSA-NCAM, and L1 as learning-modulated molecules critically involved in remodeling processes underlying associative motor-memories formation. Frontiers Media S.A. 2022-12-21 /pmc/articles/PMC9811386/ /pubmed/36620194 http://dx.doi.org/10.3389/fnana.2022.1082701 Text en Copyright © 2022 Navarro-López, Contreras, Touyarot, Herrero, Venero, Cambon, Gruart, Delgado-García, Sandi and Jiménez-Díaz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroanatomy
Navarro-López, Juan D.
Contreras, Ana
Touyarot, Katia
Herrero, Ana I.
Venero, César
Cambon, Karine
Gruart, Agnés
Delgado-García, José M.
Sandi, Carmen
Jiménez-Díaz, Lydia
Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title_full Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title_fullStr Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title_full_unstemmed Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title_short Acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
title_sort acquisition-dependent modulation of hippocampal neural cell adhesion molecules by associative motor learning
topic Neuroanatomy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811386/
https://www.ncbi.nlm.nih.gov/pubmed/36620194
http://dx.doi.org/10.3389/fnana.2022.1082701
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