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Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones
G protein–coupled receptors (GPCRs) play a fundamental role in the modulation of synaptic transmission. A pivotal example is provided by the metabotropic glutamate receptor type 4 (mGluR4), which inhibits glutamate release at presynaptic active zones (AZs). However, how GPCRs are organized within AZ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159906/ https://www.ncbi.nlm.nih.gov/pubmed/32494600 http://dx.doi.org/10.1126/sciadv.aay7193 |
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author | Siddig, Sana Aufmkolk, Sarah Doose, Sören Jobin, Marie-Lise Werner, Christian Sauer, Markus Calebiro, Davide |
author_facet | Siddig, Sana Aufmkolk, Sarah Doose, Sören Jobin, Marie-Lise Werner, Christian Sauer, Markus Calebiro, Davide |
author_sort | Siddig, Sana |
collection | PubMed |
description | G protein–coupled receptors (GPCRs) play a fundamental role in the modulation of synaptic transmission. A pivotal example is provided by the metabotropic glutamate receptor type 4 (mGluR4), which inhibits glutamate release at presynaptic active zones (AZs). However, how GPCRs are organized within AZs to regulate neurotransmission remains largely unknown. Here, we applied two-color super-resolution imaging by direct stochastic optical reconstruction microscopy (dSTORM) to investigate the nanoscale organization of mGluR4 at parallel fiber AZs in the mouse cerebellum. We find an inhomogeneous distribution, with multiple nanodomains inside AZs, each containing, on average, one to two mGluR4 subunits. Within these nanodomains, mGluR4s are often localized in close proximity to voltage-dependent Ca(V)2.1 channels and Munc-18-1, which are both essential for neurotransmitter release. These findings provide previously unknown insights into the molecular organization of GPCRs at AZs, suggesting a likely implication of a close association between mGluR4 and the secretory machinery in modulating synaptic transmission. |
format | Online Article Text |
id | pubmed-7159906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71599062020-06-02 Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones Siddig, Sana Aufmkolk, Sarah Doose, Sören Jobin, Marie-Lise Werner, Christian Sauer, Markus Calebiro, Davide Sci Adv Research Articles G protein–coupled receptors (GPCRs) play a fundamental role in the modulation of synaptic transmission. A pivotal example is provided by the metabotropic glutamate receptor type 4 (mGluR4), which inhibits glutamate release at presynaptic active zones (AZs). However, how GPCRs are organized within AZs to regulate neurotransmission remains largely unknown. Here, we applied two-color super-resolution imaging by direct stochastic optical reconstruction microscopy (dSTORM) to investigate the nanoscale organization of mGluR4 at parallel fiber AZs in the mouse cerebellum. We find an inhomogeneous distribution, with multiple nanodomains inside AZs, each containing, on average, one to two mGluR4 subunits. Within these nanodomains, mGluR4s are often localized in close proximity to voltage-dependent Ca(V)2.1 channels and Munc-18-1, which are both essential for neurotransmitter release. These findings provide previously unknown insights into the molecular organization of GPCRs at AZs, suggesting a likely implication of a close association between mGluR4 and the secretory machinery in modulating synaptic transmission. American Association for the Advancement of Science 2020-04-15 /pmc/articles/PMC7159906/ /pubmed/32494600 http://dx.doi.org/10.1126/sciadv.aay7193 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Siddig, Sana Aufmkolk, Sarah Doose, Sören Jobin, Marie-Lise Werner, Christian Sauer, Markus Calebiro, Davide Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title | Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title_full | Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title_fullStr | Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title_full_unstemmed | Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title_short | Super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
title_sort | super-resolution imaging reveals the nanoscale organization of metabotropic glutamate receptors at presynaptic active zones |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159906/ https://www.ncbi.nlm.nih.gov/pubmed/32494600 http://dx.doi.org/10.1126/sciadv.aay7193 |
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