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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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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 |
format | Online Article Text |
id | pubmed-4270082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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