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Physical determinants of vesicle mobility and supply at a central synapse
Encoding continuous sensory variables requires sustained synaptic signalling. At several sensory synapses, rapid vesicle supply is achieved via highly mobile vesicles and specialized ribbon structures, but how this is achieved at central synapses without ribbons is unclear. Here we examine vesicle m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025287/ https://www.ncbi.nlm.nih.gov/pubmed/27542193 http://dx.doi.org/10.7554/eLife.15133 |
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author | Rothman, Jason Seth Kocsis, Laszlo Herzog, Etienne Nusser, Zoltan Silver, Robin Angus |
author_facet | Rothman, Jason Seth Kocsis, Laszlo Herzog, Etienne Nusser, Zoltan Silver, Robin Angus |
author_sort | Rothman, Jason Seth |
collection | PubMed |
description | Encoding continuous sensory variables requires sustained synaptic signalling. At several sensory synapses, rapid vesicle supply is achieved via highly mobile vesicles and specialized ribbon structures, but how this is achieved at central synapses without ribbons is unclear. Here we examine vesicle mobility at excitatory cerebellar mossy fibre synapses which sustain transmission over a broad frequency bandwidth. Fluorescent recovery after photobleaching in slices from VGLUT1(Venus) knock-in mice reveal 75% of VGLUT1-containing vesicles have a high mobility, comparable to that at ribbon synapses. Experimentally constrained models establish hydrodynamic interactions and vesicle collisions are major determinants of vesicle mobility in crowded presynaptic terminals. Moreover, models incorporating 3D reconstructions of vesicle clouds near active zones (AZs) predict the measured releasable pool size and replenishment rate from the reserve pool. They also show that while vesicle reloading at AZs is not diffusion-limited at the onset of release, diffusion limits vesicle reloading during sustained high-frequency signalling. DOI: http://dx.doi.org/10.7554/eLife.15133.001 |
format | Online Article Text |
id | pubmed-5025287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50252872016-09-20 Physical determinants of vesicle mobility and supply at a central synapse Rothman, Jason Seth Kocsis, Laszlo Herzog, Etienne Nusser, Zoltan Silver, Robin Angus eLife Neuroscience Encoding continuous sensory variables requires sustained synaptic signalling. At several sensory synapses, rapid vesicle supply is achieved via highly mobile vesicles and specialized ribbon structures, but how this is achieved at central synapses without ribbons is unclear. Here we examine vesicle mobility at excitatory cerebellar mossy fibre synapses which sustain transmission over a broad frequency bandwidth. Fluorescent recovery after photobleaching in slices from VGLUT1(Venus) knock-in mice reveal 75% of VGLUT1-containing vesicles have a high mobility, comparable to that at ribbon synapses. Experimentally constrained models establish hydrodynamic interactions and vesicle collisions are major determinants of vesicle mobility in crowded presynaptic terminals. Moreover, models incorporating 3D reconstructions of vesicle clouds near active zones (AZs) predict the measured releasable pool size and replenishment rate from the reserve pool. They also show that while vesicle reloading at AZs is not diffusion-limited at the onset of release, diffusion limits vesicle reloading during sustained high-frequency signalling. DOI: http://dx.doi.org/10.7554/eLife.15133.001 eLife Sciences Publications, Ltd 2016-08-19 /pmc/articles/PMC5025287/ /pubmed/27542193 http://dx.doi.org/10.7554/eLife.15133 Text en © 2016, Rothman et al 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 Rothman, Jason Seth Kocsis, Laszlo Herzog, Etienne Nusser, Zoltan Silver, Robin Angus Physical determinants of vesicle mobility and supply at a central synapse |
title | Physical determinants of vesicle mobility and supply at a central synapse |
title_full | Physical determinants of vesicle mobility and supply at a central synapse |
title_fullStr | Physical determinants of vesicle mobility and supply at a central synapse |
title_full_unstemmed | Physical determinants of vesicle mobility and supply at a central synapse |
title_short | Physical determinants of vesicle mobility and supply at a central synapse |
title_sort | physical determinants of vesicle mobility and supply at a central synapse |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025287/ https://www.ncbi.nlm.nih.gov/pubmed/27542193 http://dx.doi.org/10.7554/eLife.15133 |
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