Na+/H+ exchange via the Drosophila vesicular glutamate transporter mediates activity‐induced acid efflux from presynaptic terminals

• Published in: The Journal of physiology Vol. 595; no. 3; pp. 805 - 824
• Main Authors: Rossano, Adam J., Kato, Akira, Minard, Karyl I., Romero, Michael F., Macleod, Gregory T.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01-02-2017; John Wiley and Sons Inc
• Subjects: Acids; Animals; Cellular and Molecular Neuroscience; Cytosol - physiology; Dissection; Drosophila; Hydrogen - physiology; Hydrogen-Ion Concentration; Insects; ion transport; Larva; Membrane Physiology; motor nerve terminal; Motor Neurons - physiology; Neuroscience ‐ Cellular/Molecular; Oocytes; pH regulation; Presynaptic Terminals - physiology; Proteins; Research Paper; Sodium - physiology; Sodium-Hydrogen Exchangers - physiology; Vesicular Glutamate Transport Proteins - physiology; Xenopus laevis; pH regulation; motor nerve terminal; ion transport
• ISSN: 0022-3751; 1469-7793
• DOI: 10.1113/JP273105

Key points
Intracellular pH regulation is vital to neurons as nerve activity produces large and rapid acid loads in presynaptic terminals.
Rapid clearance of acid loads is necessary to maintain control of neurotransmission, but neuronal acid clearance mechanisms remain poorly understood.
Glutamate is loaded into synaptic vesicles via the vesicular glutamate transporter (VGLUT), a mechanism conserved across phyla, and this study reports a previously unknown role for VGLUT as an acid‐extruding protein when deposited in the plasmamembrane during exocytosis.
The finding was made in Drosophila (fruit fly) larval motor neurons through a combined pharamacological and genetic dissection of presynaptic pH homeostatic mechanisms.
A dual role for VGLUT serves to integrate neuronal activity and pH regulation in presynaptic nerve terminals.
Neuronal activity can result in transient acidification of presynaptic terminals, and such shifts in cytosolic pH (pHcyto) probably influence mechanisms underlying forms of synaptic plasticity with a presynaptic locus. As neuronal activity drives acid loading in presynaptic terminals, we hypothesized that the same activity might drive acid efflux mechanisms to maintain pHcyto homeostasis. To better understand the integration of neuronal activity and pHcyto regulation we investigated the acid extrusion mechanisms at Drosophila glutamatergic motorneuron terminals. Expression of a fluorescent genetically encoded pH indicator, named ‘pHerry’, in the presynaptic cytosol revealed acid efflux following nerve activity to be greater than that predicted from measurements of the intrinsic rate of acid efflux. Analysis of activity‐induced acid transients in terminals deficient in either endocytosis or exocytosis revealed an acid efflux mechanism reliant upon synaptic vesicle exocytosis. Pharmacological and genetic dissection in situ and in a heterologous expression system indicate that this acid efflux is mediated by conventional plasmamembrane acid transporters, and also by previously unrecognized intrinsic H+/Na+ exchange via the Drosophila vesicular glutamate transporter (DVGLUT). DVGLUT functions not only as a vesicular glutamate transporter but also serves as an acid‐extruding protein when deposited on the plasmamembrane.
Key points
Intracellular pH regulation is vital to neurons as nerve activity produces large and rapid acid loads in presynaptic terminals.
Rapid clearance of acid loads is necessary to maintain control of neurotransmission, but neuronal acid clearance mechanisms remain poorly understood.
Glutamate is loaded into synaptic vesicles via the vesicular glutamate transporter (VGLUT), a mechanism conserved across phyla, and this study reports a previously unknown role for VGLUT as an acid‐extruding protein when deposited in the plasmamembrane during exocytosis.
The finding was made in Drosophila (fruit fly) larval motor neurons through a combined pharamacological and genetic dissection of presynaptic pH homeostatic mechanisms.
A dual role for VGLUT serves to integrate neuronal activity and pH regulation in presynaptic nerve terminals.