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Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone

The balance between fast synchronous and delayed asynchronous release of neurotransmitters has a major role in defining computational properties of neuronal synapses and regulation of neuronal network activity. However, how it is tuned at the single synapse level remains poorly understood. Here, usi...

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Autores principales: Mendonça, Philipe R. F., Tagliatti, Erica, Langley, Helen, Kotzadimitriou, Dimitrios, Zamora-Chimal, Criseida G., Timofeeva, Yulia, Volynski, Kirill E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206079/
https://www.ncbi.nlm.nih.gov/pubmed/35715404
http://dx.doi.org/10.1038/s41467-022-31070-4
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author Mendonça, Philipe R. F.
Tagliatti, Erica
Langley, Helen
Kotzadimitriou, Dimitrios
Zamora-Chimal, Criseida G.
Timofeeva, Yulia
Volynski, Kirill E.
author_facet Mendonça, Philipe R. F.
Tagliatti, Erica
Langley, Helen
Kotzadimitriou, Dimitrios
Zamora-Chimal, Criseida G.
Timofeeva, Yulia
Volynski, Kirill E.
author_sort Mendonça, Philipe R. F.
collection PubMed
description The balance between fast synchronous and delayed asynchronous release of neurotransmitters has a major role in defining computational properties of neuronal synapses and regulation of neuronal network activity. However, how it is tuned at the single synapse level remains poorly understood. Here, using the fluorescent glutamate sensor SF-iGluSnFR, we image quantal vesicular release in tens to hundreds of individual synaptic outputs from single pyramidal cells with 4 millisecond temporal and 75 nm spatial resolution. We find that the ratio between synchronous and asynchronous synaptic vesicle exocytosis varies extensively among synapses supplied by the same axon, and that the synchronicity of release is reduced at low release probability synapses. We further demonstrate that asynchronous exocytosis sites are more widely distributed within the release area than synchronous sites. Together, our results reveal a universal relationship between the two major functional properties of synapses – the timing and the overall efficacy of neurotransmitter release.
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spelling pubmed-92060792022-06-19 Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone Mendonça, Philipe R. F. Tagliatti, Erica Langley, Helen Kotzadimitriou, Dimitrios Zamora-Chimal, Criseida G. Timofeeva, Yulia Volynski, Kirill E. Nat Commun Article The balance between fast synchronous and delayed asynchronous release of neurotransmitters has a major role in defining computational properties of neuronal synapses and regulation of neuronal network activity. However, how it is tuned at the single synapse level remains poorly understood. Here, using the fluorescent glutamate sensor SF-iGluSnFR, we image quantal vesicular release in tens to hundreds of individual synaptic outputs from single pyramidal cells with 4 millisecond temporal and 75 nm spatial resolution. We find that the ratio between synchronous and asynchronous synaptic vesicle exocytosis varies extensively among synapses supplied by the same axon, and that the synchronicity of release is reduced at low release probability synapses. We further demonstrate that asynchronous exocytosis sites are more widely distributed within the release area than synchronous sites. Together, our results reveal a universal relationship between the two major functional properties of synapses – the timing and the overall efficacy of neurotransmitter release. Nature Publishing Group UK 2022-06-17 /pmc/articles/PMC9206079/ /pubmed/35715404 http://dx.doi.org/10.1038/s41467-022-31070-4 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
Mendonça, Philipe R. F.
Tagliatti, Erica
Langley, Helen
Kotzadimitriou, Dimitrios
Zamora-Chimal, Criseida G.
Timofeeva, Yulia
Volynski, Kirill E.
Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title_full Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title_fullStr Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title_full_unstemmed Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title_short Asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
title_sort asynchronous glutamate release is enhanced in low release efficacy synapses and dispersed across the active zone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206079/
https://www.ncbi.nlm.nih.gov/pubmed/35715404
http://dx.doi.org/10.1038/s41467-022-31070-4
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