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Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific

Heterotetrameric glutamate receptors are essential for the development, function, and plasticity of spine synapses but how they are organized to achieve this is not known. Here we show that the nanoscale organization of glutamate receptors containing specific subunits define distinct subsynaptic fea...

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Autores principales: Hruska, Martin, Cain, Rachel E., Dalva, Matthew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854560/
https://www.ncbi.nlm.nih.gov/pubmed/35177616
http://dx.doi.org/10.1038/s41467-022-28504-4
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author Hruska, Martin
Cain, Rachel E.
Dalva, Matthew B.
author_facet Hruska, Martin
Cain, Rachel E.
Dalva, Matthew B.
author_sort Hruska, Martin
collection PubMed
description Heterotetrameric glutamate receptors are essential for the development, function, and plasticity of spine synapses but how they are organized to achieve this is not known. Here we show that the nanoscale organization of glutamate receptors containing specific subunits define distinct subsynaptic features. Glutamate receptors containing GluA2 or GluN1 subunits establish nanomodular elements precisely positioned relative to Synaptotagmin-1 positive presynaptic release sites that scale with spine size. Glutamate receptors containing GluA1 or GluN2B specify features that exhibit flexibility: GluA1-subunit containing AMPARs are found in larger spines, while GluN2B-subunit containing NMDARs are enriched in the smallest spines with neither following a strict modular organization. Given that the precise positioning of distinct classes of glutamate receptors is linked to diverse events including cell death and synaptic plasticity, this unexpectedly robust synaptic nanoarchitecture provides a resilient system, where nanopositioned glutamate receptor heterotetramers define specific subsynaptic regions of individual spine synapses.
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spelling pubmed-88545602022-03-04 Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific Hruska, Martin Cain, Rachel E. Dalva, Matthew B. Nat Commun Article Heterotetrameric glutamate receptors are essential for the development, function, and plasticity of spine synapses but how they are organized to achieve this is not known. Here we show that the nanoscale organization of glutamate receptors containing specific subunits define distinct subsynaptic features. Glutamate receptors containing GluA2 or GluN1 subunits establish nanomodular elements precisely positioned relative to Synaptotagmin-1 positive presynaptic release sites that scale with spine size. Glutamate receptors containing GluA1 or GluN2B specify features that exhibit flexibility: GluA1-subunit containing AMPARs are found in larger spines, while GluN2B-subunit containing NMDARs are enriched in the smallest spines with neither following a strict modular organization. Given that the precise positioning of distinct classes of glutamate receptors is linked to diverse events including cell death and synaptic plasticity, this unexpectedly robust synaptic nanoarchitecture provides a resilient system, where nanopositioned glutamate receptor heterotetramers define specific subsynaptic regions of individual spine synapses. Nature Publishing Group UK 2022-02-17 /pmc/articles/PMC8854560/ /pubmed/35177616 http://dx.doi.org/10.1038/s41467-022-28504-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hruska, Martin
Cain, Rachel E.
Dalva, Matthew B.
Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title_full Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title_fullStr Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title_full_unstemmed Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title_short Nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
title_sort nanoscale rules governing the organization of glutamate receptors in spine synapses are subunit specific
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8854560/
https://www.ncbi.nlm.nih.gov/pubmed/35177616
http://dx.doi.org/10.1038/s41467-022-28504-4
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