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Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence
Endocytosis is an essential process at sites of synaptic release. Not only are synaptic vesicles recycled by endocytosis, but the removal of proteins and lipids by endocytosis is needed to restore release site function at active zones after vesicle fusion. Synaptic exocytosis from vertebrate photore...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881445/ https://www.ncbi.nlm.nih.gov/pubmed/29555658 http://dx.doi.org/10.1085/jgp.201711919 |
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author | Wen, Xiangyi Van Hook, Matthew J. Grassmeyer, Justin J. Wiesman, Alex I. Rich, Grace M. Cork, Karlene M. Thoreson, Wallace B. |
author_facet | Wen, Xiangyi Van Hook, Matthew J. Grassmeyer, Justin J. Wiesman, Alex I. Rich, Grace M. Cork, Karlene M. Thoreson, Wallace B. |
author_sort | Wen, Xiangyi |
collection | PubMed |
description | Endocytosis is an essential process at sites of synaptic release. Not only are synaptic vesicles recycled by endocytosis, but the removal of proteins and lipids by endocytosis is needed to restore release site function at active zones after vesicle fusion. Synaptic exocytosis from vertebrate photoreceptors involves synaptic ribbons that serve to cluster vesicles near the presynaptic membrane. In this study, we hypothesize that this clustering increases the likelihood that exocytosis at one ribbon release site may disrupt release at an adjacent site and therefore that endocytosis may be particularly important for restoring release site competence at photoreceptor ribbon synapses. To test this, we combined optical and electrophysiological techniques in salamander rods. Pharmacological inhibition of dynamin-dependent endocytosis rapidly inhibits release from synaptic ribbons and slows recovery of ribbon-mediated release from paired pulse synaptic depression. Inhibiting endocytosis impairs the ability of second-order horizontal cells to follow rod light responses at frequencies as low as 2 Hz. Inhibition of endocytosis also increases lateral membrane mobility of individual Ca(2+) channels, showing that it changes release site structure. Visualization of single synaptic vesicles by total internal reflection fluorescence microscopy reveals that inhibition of endocytosis reduces the likelihood of fusion among vesicles docked near ribbons and increases the likelihood that they will retreat from the membrane without fusion. Vesicle advance toward the membrane is also reduced, but the number of membrane-associated vesicles is not. Endocytosis therefore appears to be more important for restoring later steps in vesicle fusion than for restoring docking. Unlike conventional synapses in which endocytic restoration of release sites is evident only at high frequencies, endocytosis is needed to maintain release from rod ribbon synapses even at modest frequencies. |
format | Online Article Text |
id | pubmed-5881445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58814452018-10-02 Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence Wen, Xiangyi Van Hook, Matthew J. Grassmeyer, Justin J. Wiesman, Alex I. Rich, Grace M. Cork, Karlene M. Thoreson, Wallace B. J Gen Physiol Research Articles Endocytosis is an essential process at sites of synaptic release. Not only are synaptic vesicles recycled by endocytosis, but the removal of proteins and lipids by endocytosis is needed to restore release site function at active zones after vesicle fusion. Synaptic exocytosis from vertebrate photoreceptors involves synaptic ribbons that serve to cluster vesicles near the presynaptic membrane. In this study, we hypothesize that this clustering increases the likelihood that exocytosis at one ribbon release site may disrupt release at an adjacent site and therefore that endocytosis may be particularly important for restoring release site competence at photoreceptor ribbon synapses. To test this, we combined optical and electrophysiological techniques in salamander rods. Pharmacological inhibition of dynamin-dependent endocytosis rapidly inhibits release from synaptic ribbons and slows recovery of ribbon-mediated release from paired pulse synaptic depression. Inhibiting endocytosis impairs the ability of second-order horizontal cells to follow rod light responses at frequencies as low as 2 Hz. Inhibition of endocytosis also increases lateral membrane mobility of individual Ca(2+) channels, showing that it changes release site structure. Visualization of single synaptic vesicles by total internal reflection fluorescence microscopy reveals that inhibition of endocytosis reduces the likelihood of fusion among vesicles docked near ribbons and increases the likelihood that they will retreat from the membrane without fusion. Vesicle advance toward the membrane is also reduced, but the number of membrane-associated vesicles is not. Endocytosis therefore appears to be more important for restoring later steps in vesicle fusion than for restoring docking. Unlike conventional synapses in which endocytic restoration of release sites is evident only at high frequencies, endocytosis is needed to maintain release from rod ribbon synapses even at modest frequencies. Rockefeller University Press 2018-04-02 /pmc/articles/PMC5881445/ /pubmed/29555658 http://dx.doi.org/10.1085/jgp.201711919 Text en © 2018 Wen et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Wen, Xiangyi Van Hook, Matthew J. Grassmeyer, Justin J. Wiesman, Alex I. Rich, Grace M. Cork, Karlene M. Thoreson, Wallace B. Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title | Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title_full | Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title_fullStr | Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title_full_unstemmed | Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title_short | Endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
title_sort | endocytosis sustains release at photoreceptor ribbon synapses by restoring fusion competence |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881445/ https://www.ncbi.nlm.nih.gov/pubmed/29555658 http://dx.doi.org/10.1085/jgp.201711919 |
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