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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...

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Autores principales: Scheefhals, Nicky, Westra, Manon, MacGillavry, Harold D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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.
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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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