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NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition
NMDA ionotropic glutamate receptors (NMDARs) are crucial in activity-dependent synaptic changes and in learning and memory. NMDARs are composed of two GluN1 essential subunits and two regulatory subunits which define their pharmacological and physiological profile. In CNS structures involved in cogn...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863338/ https://www.ncbi.nlm.nih.gov/pubmed/29706992 http://dx.doi.org/10.1155/2018/5093048 |
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author | Baez, María Verónica Cercato, Magalí Cecilia Jerusalinsky, Diana Alicia |
author_facet | Baez, María Verónica Cercato, Magalí Cecilia Jerusalinsky, Diana Alicia |
author_sort | Baez, María Verónica |
collection | PubMed |
description | NMDA ionotropic glutamate receptors (NMDARs) are crucial in activity-dependent synaptic changes and in learning and memory. NMDARs are composed of two GluN1 essential subunits and two regulatory subunits which define their pharmacological and physiological profile. In CNS structures involved in cognitive functions as the hippocampus and prefrontal cortex, GluN2A and GluN2B are major regulatory subunits; their expression is dynamic and tightly regulated, but little is known about specific changes after plasticity induction or memory acquisition. Data strongly suggest that following appropriate stimulation, there is a rapid increase in surface GluN2A-NMDAR at the postsynapses, attributed to lateral receptor mobilization from adjacent locations. Whenever synaptic plasticity is induced or memory is consolidated, more GluN2A-NMDARs are assembled likely using GluN2A from a local translation and GluN1 from local ER. Later on, NMDARs are mobilized from other pools, and there are de novo syntheses at the neuron soma. Changes in GluN1 or NMDAR levels induced by synaptic plasticity and by spatial memory formation seem to occur in different waves of NMDAR transport/expression/degradation, with a net increase at the postsynaptic side and a rise in expression at both the spine and neuronal soma. This review aims to put together that information and the proposed hypotheses. |
format | Online Article Text |
id | pubmed-5863338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58633382018-04-29 NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition Baez, María Verónica Cercato, Magalí Cecilia Jerusalinsky, Diana Alicia Neural Plast Review Article NMDA ionotropic glutamate receptors (NMDARs) are crucial in activity-dependent synaptic changes and in learning and memory. NMDARs are composed of two GluN1 essential subunits and two regulatory subunits which define their pharmacological and physiological profile. In CNS structures involved in cognitive functions as the hippocampus and prefrontal cortex, GluN2A and GluN2B are major regulatory subunits; their expression is dynamic and tightly regulated, but little is known about specific changes after plasticity induction or memory acquisition. Data strongly suggest that following appropriate stimulation, there is a rapid increase in surface GluN2A-NMDAR at the postsynapses, attributed to lateral receptor mobilization from adjacent locations. Whenever synaptic plasticity is induced or memory is consolidated, more GluN2A-NMDARs are assembled likely using GluN2A from a local translation and GluN1 from local ER. Later on, NMDARs are mobilized from other pools, and there are de novo syntheses at the neuron soma. Changes in GluN1 or NMDAR levels induced by synaptic plasticity and by spatial memory formation seem to occur in different waves of NMDAR transport/expression/degradation, with a net increase at the postsynaptic side and a rise in expression at both the spine and neuronal soma. This review aims to put together that information and the proposed hypotheses. Hindawi 2018-03-07 /pmc/articles/PMC5863338/ /pubmed/29706992 http://dx.doi.org/10.1155/2018/5093048 Text en Copyright © 2018 María Verónica Baez et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Baez, María Verónica Cercato, Magalí Cecilia Jerusalinsky, Diana Alicia NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title | NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title_full | NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title_fullStr | NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title_full_unstemmed | NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title_short | NMDA Receptor Subunits Change after Synaptic Plasticity Induction and Learning and Memory Acquisition |
title_sort | nmda receptor subunits change after synaptic plasticity induction and learning and memory acquisition |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863338/ https://www.ncbi.nlm.nih.gov/pubmed/29706992 http://dx.doi.org/10.1155/2018/5093048 |
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