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Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement
Cell adhesion molecules and downstream growth factor-dependent signaling are critical for brain development and synaptic plasticity, and they have been linked to cognitive function in adult animals. We have previously developed a mimetic peptide (FGL) from the neural cell adhesion molecule (NCAM) th...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283560/ https://www.ncbi.nlm.nih.gov/pubmed/22363206 http://dx.doi.org/10.1371/journal.pbio.1001262 |
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author | Knafo, Shira Venero, César Sánchez-Puelles, Cristina Pereda-Peréz, Inmaculada Franco, Ana Sandi, Carmen Suárez, Luz M. Solís, José M. Alonso-Nanclares, Lidia Martín, Eduardo D. Merino-Serrais, Paula Borcel, Erika Li, Shizhong Chen, Yongshuo Gonzalez-Soriano, Juncal Berezin, Vladimir Bock, Elisabeth DeFelipe, Javier Esteban, José A. |
author_facet | Knafo, Shira Venero, César Sánchez-Puelles, Cristina Pereda-Peréz, Inmaculada Franco, Ana Sandi, Carmen Suárez, Luz M. Solís, José M. Alonso-Nanclares, Lidia Martín, Eduardo D. Merino-Serrais, Paula Borcel, Erika Li, Shizhong Chen, Yongshuo Gonzalez-Soriano, Juncal Berezin, Vladimir Bock, Elisabeth DeFelipe, Javier Esteban, José A. |
author_sort | Knafo, Shira |
collection | PubMed |
description | Cell adhesion molecules and downstream growth factor-dependent signaling are critical for brain development and synaptic plasticity, and they have been linked to cognitive function in adult animals. We have previously developed a mimetic peptide (FGL) from the neural cell adhesion molecule (NCAM) that enhances spatial learning and memory in rats. We have now investigated the cellular and molecular basis of this cognitive enhancement, using biochemical, morphological, electrophysiological, and behavioral analyses. We have found that FGL triggers a long-lasting enhancement of synaptic transmission in hippocampal CA1 neurons. This effect is mediated by a facilitated synaptic delivery of AMPA receptors, which is accompanied by enhanced NMDA receptor-dependent long-term potentiation (LTP). Both LTP and cognitive enhancement are mediated by an initial PKC activation, which is followed by persistent CaMKII activation. These results provide a mechanistic link between facilitation of AMPA receptor synaptic delivery and improved hippocampal-dependent learning, induced by a pharmacological cognitive enhancer. |
format | Online Article Text |
id | pubmed-3283560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32835602012-02-23 Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement Knafo, Shira Venero, César Sánchez-Puelles, Cristina Pereda-Peréz, Inmaculada Franco, Ana Sandi, Carmen Suárez, Luz M. Solís, José M. Alonso-Nanclares, Lidia Martín, Eduardo D. Merino-Serrais, Paula Borcel, Erika Li, Shizhong Chen, Yongshuo Gonzalez-Soriano, Juncal Berezin, Vladimir Bock, Elisabeth DeFelipe, Javier Esteban, José A. PLoS Biol Research Article Cell adhesion molecules and downstream growth factor-dependent signaling are critical for brain development and synaptic plasticity, and they have been linked to cognitive function in adult animals. We have previously developed a mimetic peptide (FGL) from the neural cell adhesion molecule (NCAM) that enhances spatial learning and memory in rats. We have now investigated the cellular and molecular basis of this cognitive enhancement, using biochemical, morphological, electrophysiological, and behavioral analyses. We have found that FGL triggers a long-lasting enhancement of synaptic transmission in hippocampal CA1 neurons. This effect is mediated by a facilitated synaptic delivery of AMPA receptors, which is accompanied by enhanced NMDA receptor-dependent long-term potentiation (LTP). Both LTP and cognitive enhancement are mediated by an initial PKC activation, which is followed by persistent CaMKII activation. These results provide a mechanistic link between facilitation of AMPA receptor synaptic delivery and improved hippocampal-dependent learning, induced by a pharmacological cognitive enhancer. Public Library of Science 2012-02-21 /pmc/articles/PMC3283560/ /pubmed/22363206 http://dx.doi.org/10.1371/journal.pbio.1001262 Text en Knafo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Knafo, Shira Venero, César Sánchez-Puelles, Cristina Pereda-Peréz, Inmaculada Franco, Ana Sandi, Carmen Suárez, Luz M. Solís, José M. Alonso-Nanclares, Lidia Martín, Eduardo D. Merino-Serrais, Paula Borcel, Erika Li, Shizhong Chen, Yongshuo Gonzalez-Soriano, Juncal Berezin, Vladimir Bock, Elisabeth DeFelipe, Javier Esteban, José A. Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title | Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title_full | Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title_fullStr | Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title_full_unstemmed | Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title_short | Facilitation of AMPA Receptor Synaptic Delivery as a Molecular Mechanism for Cognitive Enhancement |
title_sort | facilitation of ampa receptor synaptic delivery as a molecular mechanism for cognitive enhancement |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283560/ https://www.ncbi.nlm.nih.gov/pubmed/22363206 http://dx.doi.org/10.1371/journal.pbio.1001262 |
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