The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery

Author:

Poëa-Guyon Sandrine1,Ammar Mohamed Raafet2,Erard Marie3,Amar Muriel1,Moreau Alexandre W.,Fossier Philippe1,Gleize Vincent1,Vitale Nicolas2,Morel Nicolas1

Affiliation:

1. Centre de Neurosciences Paris-Sud, Centre National de la Recherche Scientifique Unité Mixte de Recherche 8195 and Université Paris-Sud, F-91405 Orsay, France

2. Institut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique Unité Propre de Recherche 3212 and Université de Strasbourg, 67084 Strasbourg, France

3. Laboratoire de Chimie Physique, Centre National de la Recherche Scientifique Unité Mixte de Recherche 8000 and Université Paris-Sud, F-91405 Orsay, France

Abstract

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

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