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A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain

Glutamate receptors of the N-methyl-D-aspartate (NMDA) family are coincident detectors of pre- and postsynaptic activity, allowing Ca(2+) influx into neurons. These properties are central to neurological disease mechanisms and are proposed to be the basis of associative learning and memory. In addit...

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Autores principales: Warming, Hannah, Pegasiou, Chrysia-Maria, Pitera, Aleksandra P., Kariis, Hanna, Houghton, Steven D., Kurbatskaya, Ksenia, Ahmed, Aminul, Grundy, Paul, Vajramani, Girish, Bulters, Diederik, Altafaj, Xavier, Deinhardt, Katrin, Vargas-Caballero, Mariana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610962/
https://www.ncbi.nlm.nih.gov/pubmed/31272478
http://dx.doi.org/10.1186/s13041-019-0485-9
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author Warming, Hannah
Pegasiou, Chrysia-Maria
Pitera, Aleksandra P.
Kariis, Hanna
Houghton, Steven D.
Kurbatskaya, Ksenia
Ahmed, Aminul
Grundy, Paul
Vajramani, Girish
Bulters, Diederik
Altafaj, Xavier
Deinhardt, Katrin
Vargas-Caballero, Mariana
author_facet Warming, Hannah
Pegasiou, Chrysia-Maria
Pitera, Aleksandra P.
Kariis, Hanna
Houghton, Steven D.
Kurbatskaya, Ksenia
Ahmed, Aminul
Grundy, Paul
Vajramani, Girish
Bulters, Diederik
Altafaj, Xavier
Deinhardt, Katrin
Vargas-Caballero, Mariana
author_sort Warming, Hannah
collection PubMed
description Glutamate receptors of the N-methyl-D-aspartate (NMDA) family are coincident detectors of pre- and postsynaptic activity, allowing Ca(2+) influx into neurons. These properties are central to neurological disease mechanisms and are proposed to be the basis of associative learning and memory. In addition to the well-characterised canonical GluN2A NMDAR isoform, large-scale open reading frames in human tissues had suggested the expression of a primate-specific short GluN2A isoform referred to as GluN2A-S. Here, we confirm the expression of both GluN2A transcripts in human and primate but not rodent brain tissue, and show that they are translated to two corresponding GluN2A proteins present in human brain. Furthermore, we demonstrate that recombinant GluN2A-S co-assembles with the obligatory NMDAR subunit GluN1 to form functional NMDA receptors. These findings suggest a more complex NMDAR repertoire in human brain than previously thought.
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spelling pubmed-66109622019-07-16 A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain Warming, Hannah Pegasiou, Chrysia-Maria Pitera, Aleksandra P. Kariis, Hanna Houghton, Steven D. Kurbatskaya, Ksenia Ahmed, Aminul Grundy, Paul Vajramani, Girish Bulters, Diederik Altafaj, Xavier Deinhardt, Katrin Vargas-Caballero, Mariana Mol Brain Short Report Glutamate receptors of the N-methyl-D-aspartate (NMDA) family are coincident detectors of pre- and postsynaptic activity, allowing Ca(2+) influx into neurons. These properties are central to neurological disease mechanisms and are proposed to be the basis of associative learning and memory. In addition to the well-characterised canonical GluN2A NMDAR isoform, large-scale open reading frames in human tissues had suggested the expression of a primate-specific short GluN2A isoform referred to as GluN2A-S. Here, we confirm the expression of both GluN2A transcripts in human and primate but not rodent brain tissue, and show that they are translated to two corresponding GluN2A proteins present in human brain. Furthermore, we demonstrate that recombinant GluN2A-S co-assembles with the obligatory NMDAR subunit GluN1 to form functional NMDA receptors. These findings suggest a more complex NMDAR repertoire in human brain than previously thought. BioMed Central 2019-07-04 /pmc/articles/PMC6610962/ /pubmed/31272478 http://dx.doi.org/10.1186/s13041-019-0485-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Warming, Hannah
Pegasiou, Chrysia-Maria
Pitera, Aleksandra P.
Kariis, Hanna
Houghton, Steven D.
Kurbatskaya, Ksenia
Ahmed, Aminul
Grundy, Paul
Vajramani, Girish
Bulters, Diederik
Altafaj, Xavier
Deinhardt, Katrin
Vargas-Caballero, Mariana
A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title_full A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title_fullStr A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title_full_unstemmed A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title_short A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain
title_sort primate-specific short glun2a-nmda receptor isoform is expressed in the human brain
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610962/
https://www.ncbi.nlm.nih.gov/pubmed/31272478
http://dx.doi.org/10.1186/s13041-019-0485-9
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