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Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse

A puzzling property of synaptic transmission, originally established at the neuromuscular junction, is that the time course of transmitter release is independent of the extracellular Ca(2+) concentration ([Ca(2+)](o)), whereas the rate of release is highly [Ca(2+)](o)-dependent. Here, we examine the...

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Detalles Bibliográficos
Autores principales: Arai, Itaru, Jonas, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270082/
https://www.ncbi.nlm.nih.gov/pubmed/25487988
http://dx.doi.org/10.7554/eLife.04057
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author Arai, Itaru
Jonas, Peter
author_facet Arai, Itaru
Jonas, Peter
author_sort Arai, Itaru
collection PubMed
description A puzzling property of synaptic transmission, originally established at the neuromuscular junction, is that the time course of transmitter release is independent of the extracellular Ca(2+) concentration ([Ca(2+)](o)), whereas the rate of release is highly [Ca(2+)](o)-dependent. Here, we examine the time course of release at inhibitory basket cell-Purkinje cell synapses and show that it is independent of [Ca(2+)](o). Modeling of Ca(2+)-dependent transmitter release suggests that the invariant time course of release critically depends on tight coupling between Ca(2+) channels and release sensors. Experiments with exogenous Ca(2+) chelators reveal that channel-sensor coupling at basket cell-Purkinje cell synapses is very tight, with a mean distance of 10–20 nm. Thus, tight channel-sensor coupling provides a mechanistic explanation for the apparent [Ca(2+)](o) independence of the time course of release. DOI: http://dx.doi.org/10.7554/eLife.04057.001
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spelling pubmed-42700822015-01-29 Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse Arai, Itaru Jonas, Peter eLife Neuroscience A puzzling property of synaptic transmission, originally established at the neuromuscular junction, is that the time course of transmitter release is independent of the extracellular Ca(2+) concentration ([Ca(2+)](o)), whereas the rate of release is highly [Ca(2+)](o)-dependent. Here, we examine the time course of release at inhibitory basket cell-Purkinje cell synapses and show that it is independent of [Ca(2+)](o). Modeling of Ca(2+)-dependent transmitter release suggests that the invariant time course of release critically depends on tight coupling between Ca(2+) channels and release sensors. Experiments with exogenous Ca(2+) chelators reveal that channel-sensor coupling at basket cell-Purkinje cell synapses is very tight, with a mean distance of 10–20 nm. Thus, tight channel-sensor coupling provides a mechanistic explanation for the apparent [Ca(2+)](o) independence of the time course of release. DOI: http://dx.doi.org/10.7554/eLife.04057.001 eLife Sciences Publications, Ltd 2014-12-09 /pmc/articles/PMC4270082/ /pubmed/25487988 http://dx.doi.org/10.7554/eLife.04057 Text en Copyright © 2014, Arai and Jonas http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Arai, Itaru
Jonas, Peter
Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title_full Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title_fullStr Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title_full_unstemmed Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title_short Nanodomain coupling explains Ca(2+) independence of transmitter release time course at a fast central synapse
title_sort nanodomain coupling explains ca(2+) independence of transmitter release time course at a fast central synapse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4270082/
https://www.ncbi.nlm.nih.gov/pubmed/25487988
http://dx.doi.org/10.7554/eLife.04057
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