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The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery
Several studies have suggested that the V0 domain of the vacuolar-type H(+)-adenosine triphosphatase (V-ATPase) is directly implicated in secretory vesicle exocytosis through a role in membrane fusion. We report in this paper that there was a rapid decrease in neurotransmitter release after acute ph...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812966/ https://www.ncbi.nlm.nih.gov/pubmed/24165939 http://dx.doi.org/10.1083/jcb.201303104 |
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author | Poëa-Guyon, Sandrine Ammar, Mohamed Raafet Erard, Marie Amar, Muriel Moreau, Alexandre W. Fossier, Philippe Gleize, Vincent Vitale, Nicolas Morel, Nicolas |
author_facet | Poëa-Guyon, Sandrine Ammar, Mohamed Raafet Erard, Marie Amar, Muriel Moreau, Alexandre W. Fossier, Philippe Gleize, Vincent Vitale, Nicolas Morel, Nicolas |
author_sort | Poëa-Guyon, Sandrine |
collection | PubMed |
description | Several studies have suggested that the V0 domain of the vacuolar-type H(+)-adenosine triphosphatase (V-ATPase) is directly implicated in secretory vesicle exocytosis through a role in membrane fusion. We report in this paper that there was a rapid decrease in neurotransmitter release after acute photoinactivation of the V0 a1-I subunit in neuronal pairs. Likewise, inactivation of the V0 a1-I subunit in chromaffin cells resulted in a decreased frequency and prolonged kinetics of amperometric spikes induced by depolarization, with shortening of the fusion pore open time. Dissipation of the granular pH gradient was associated with an inhibition of exocytosis and correlated with the V1–V0 association status in secretory granules. We thus conclude that V0 serves as a sensor of intragranular pH that controls exocytosis and synaptic transmission via the reversible dissociation of V1 at acidic pH. Hence, the V-ATPase membrane domain would allow the exocytotic machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmitter reloading. |
format | Online Article Text |
id | pubmed-3812966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38129662014-04-28 The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery Poëa-Guyon, Sandrine Ammar, Mohamed Raafet Erard, Marie Amar, Muriel Moreau, Alexandre W. Fossier, Philippe Gleize, Vincent Vitale, Nicolas Morel, Nicolas J Cell Biol Research Articles Several studies have suggested that the V0 domain of the vacuolar-type H(+)-adenosine triphosphatase (V-ATPase) is directly implicated in secretory vesicle exocytosis through a role in membrane fusion. We report in this paper that there was a rapid decrease in neurotransmitter release after acute photoinactivation of the V0 a1-I subunit in neuronal pairs. Likewise, inactivation of the V0 a1-I subunit in chromaffin cells resulted in a decreased frequency and prolonged kinetics of amperometric spikes induced by depolarization, with shortening of the fusion pore open time. Dissipation of the granular pH gradient was associated with an inhibition of exocytosis and correlated with the V1–V0 association status in secretory granules. We thus conclude that V0 serves as a sensor of intragranular pH that controls exocytosis and synaptic transmission via the reversible dissociation of V1 at acidic pH. Hence, the V-ATPase membrane domain would allow the exocytotic machinery to discriminate fully loaded and acidified vesicles from vesicles undergoing neurotransmitter reloading. The Rockefeller University Press 2013-10-28 /pmc/articles/PMC3812966/ /pubmed/24165939 http://dx.doi.org/10.1083/jcb.201303104 Text en © 2013 Poëa-Guyon et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Poëa-Guyon, Sandrine Ammar, Mohamed Raafet Erard, Marie Amar, Muriel Moreau, Alexandre W. Fossier, Philippe Gleize, Vincent Vitale, Nicolas Morel, Nicolas The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title | The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title_full | The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title_fullStr | The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title_full_unstemmed | The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title_short | The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery |
title_sort | v-atpase membrane domain is a sensor of granular ph that controls the exocytotic machinery |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812966/ https://www.ncbi.nlm.nih.gov/pubmed/24165939 http://dx.doi.org/10.1083/jcb.201303104 |
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