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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...

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Autores principales: Poëa-Guyon, Sandrine, Ammar, Mohamed Raafet, Erard, Marie, Amar, Muriel, Moreau, Alexandre W., Fossier, Philippe, Gleize, Vincent, Vitale, Nicolas, Morel, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
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.
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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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