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mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function
The unique perisynaptic distribution of postsynaptic metabotropic glutamate receptors (mGluRs) at excitatory synapses is predicted to directly shape synaptic function, but mechanistic insight into how this distribution is regulated and impacts synaptic signaling is lacking. We used live-cell and sup...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842668/ https://www.ncbi.nlm.nih.gov/pubmed/36646691 http://dx.doi.org/10.1038/s41467-022-35680-w |
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author | Scheefhals, Nicky Westra, Manon MacGillavry, Harold D. |
author_facet | Scheefhals, Nicky Westra, Manon MacGillavry, Harold D. |
author_sort | Scheefhals, Nicky |
collection | PubMed |
description | The unique perisynaptic distribution of postsynaptic metabotropic glutamate receptors (mGluRs) at excitatory synapses is predicted to directly shape synaptic function, but mechanistic insight into how this distribution is regulated and impacts synaptic signaling is lacking. We used live-cell and super-resolution imaging approaches, and developed molecular tools to resolve and acutely manipulate the dynamic nanoscale distribution of mGluR5. Here we show that mGluR5 is dynamically organized in perisynaptic nanodomains that localize close to, but not in the synapse. The C-terminal domain of mGluR5 critically controlled perisynaptic confinement and prevented synaptic entry. We developed an inducible interaction system to overcome synaptic exclusion of mGluR5 and investigate the impact on synaptic function. We found that mGluR5 recruitment to the synapse acutely increased synaptic calcium responses. Altogether, we propose that transient confinement of mGluR5 in perisynaptic nanodomains allows flexible modulation of synaptic function. |
format | Online Article Text |
id | pubmed-9842668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98426682023-01-18 mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function Scheefhals, Nicky Westra, Manon MacGillavry, Harold D. Nat Commun Article The unique perisynaptic distribution of postsynaptic metabotropic glutamate receptors (mGluRs) at excitatory synapses is predicted to directly shape synaptic function, but mechanistic insight into how this distribution is regulated and impacts synaptic signaling is lacking. We used live-cell and super-resolution imaging approaches, and developed molecular tools to resolve and acutely manipulate the dynamic nanoscale distribution of mGluR5. Here we show that mGluR5 is dynamically organized in perisynaptic nanodomains that localize close to, but not in the synapse. The C-terminal domain of mGluR5 critically controlled perisynaptic confinement and prevented synaptic entry. We developed an inducible interaction system to overcome synaptic exclusion of mGluR5 and investigate the impact on synaptic function. We found that mGluR5 recruitment to the synapse acutely increased synaptic calcium responses. Altogether, we propose that transient confinement of mGluR5 in perisynaptic nanodomains allows flexible modulation of synaptic function. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842668/ /pubmed/36646691 http://dx.doi.org/10.1038/s41467-022-35680-w Text en © The Author(s) 2023 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 Scheefhals, Nicky Westra, Manon MacGillavry, Harold D. mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title | mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title_full | mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title_fullStr | mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title_full_unstemmed | mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title_short | mGluR5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
title_sort | mglur5 is transiently confined in perisynaptic nanodomains to shape synaptic function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842668/ https://www.ncbi.nlm.nih.gov/pubmed/36646691 http://dx.doi.org/10.1038/s41467-022-35680-w |
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