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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8854560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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