| Literature DB >> 30155790 |
Sylvain Rama1,2, Norah Boumedine-Guignon1,2, Marion Sangiardi1,2, Fahamoe Youssouf1,2, Yves Maulet1,2, Christian Lévêque1,2, Maya Belghazi2,3, Michael Seagar1,2, Dominique Debanne1,2, Oussama El Far4,5.
Abstract
Synaptic vesicle proton V-ATPase is an essential component in synaptic vesicle function. Active acidification of synaptic vesicles, triggered by the V-ATPase, is necessary for neurotransmitter storage. Independently from its proton transport activity, an additional important function of the membrane-embedded sector of the V-ATPase has been uncovered over recent years. Subunits a and c of the membrane sector of this multi-molecular complex have been shown to interact with SNARE proteins and to be involved in modulating neurotransmitter release. The c-subunit interacts with the v-SNARE VAMP2 and facilitates neurotransmission. In this study, we used chromophore-assisted light inactivation and monitored the consequences on neurotransmission on line in CA3 pyramidal neurons. We show that V-ATPase c-subunit V0c is a key element in modulating neurotransmission and that its specific inactivation rapidly inhibited neurotransmission.Entities:
Keywords: Chromophore-assisted light inactivation (CALI); GeneGun; Hippocampal organotypic slice culture; Neurons; Neurotransmission; V-ATPase
Mesh:
Substances:
Year: 2018 PMID: 30155790 DOI: 10.1007/s12035-018-1324-1
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590