Spontaneous Vesicle Recycling in the Synaptic Bouton

The trigger for synaptic vesicle exocytosis is Ca2+, which enters the synaptic bouton following action potential stimulation. However, spontaneous release of neurotransmitter also occurs in the absence of stimulation in virtually all synaptic boutons. It has long been thought that this represents ex...

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Main Authors: Sven eTruckenbrodt, Silvio O Rizzoli
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-12-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00409/full
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spelling doaj-bad47b3a305b4998ab27401a914518d02020-11-24T23:04:23ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-12-01810.3389/fncel.2014.00409119954Spontaneous Vesicle Recycling in the Synaptic BoutonSven eTruckenbrodt0Sven eTruckenbrodt1Sven eTruckenbrodt2Silvio O Rizzoli3Silvio O Rizzoli4University of Göttingen Medical CenterEuropean Neuroscience Institute GöttingenIMPRS for Molecular BiologyUniversity of Göttingen Medical CenterEuropean Neuroscience Institute GöttingenThe trigger for synaptic vesicle exocytosis is Ca2+, which enters the synaptic bouton following action potential stimulation. However, spontaneous release of neurotransmitter also occurs in the absence of stimulation in virtually all synaptic boutons. It has long been thought that this represents exocytosis driven by fluctuations in local Ca2+ levels. The vesicles responding to these fluctuations are thought to be the same ones that release upon stimulation, albeit potentially triggered by different Ca2+ sensors. This view has been challenged by several recent works, which have suggested that spontaneous release is driven by a separate pool of synaptic vesicles. Numerous articles appeared during the last few years in support of each of these hypotheses, and it has been challenging to bring them into accord. We speculate here on the origins of this controversy, and propose a solution that is related to developmental effects. Constitutive membrane traffic, needed for the biogenesis of vesicles and synapses, is responsible for high levels of spontaneous membrane fusion in young neurons, probably independent of Ca2+. The vesicles releasing spontaneously in such neurons are not related to other synaptic vesicle pools and may represent constitutively releasing vesicles (CRVs) rather than bona fide synaptic vesicles. In mature neurons, constitutive traffic is much dampened, and the few remaining spontaneous release events probably represent bona fide spontaneously releasing synaptic vesicles (SRSVs) responding to Ca2+ fluctuations, along with a handful of CRVs that participate in synaptic vesicle turnover.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00409/fullsynapse developmentspontaneous releasesynaptic vesicle poolssynaptic vesicle recyclingsynaptic vesicle biogenesis
collection DOAJ
language English
format Article
sources DOAJ
author Sven eTruckenbrodt
Sven eTruckenbrodt
Sven eTruckenbrodt
Silvio O Rizzoli
Silvio O Rizzoli
spellingShingle Sven eTruckenbrodt
Sven eTruckenbrodt
Sven eTruckenbrodt
Silvio O Rizzoli
Silvio O Rizzoli
Spontaneous Vesicle Recycling in the Synaptic Bouton
Frontiers in Cellular Neuroscience
synapse development
spontaneous release
synaptic vesicle pools
synaptic vesicle recycling
synaptic vesicle biogenesis
author_facet Sven eTruckenbrodt
Sven eTruckenbrodt
Sven eTruckenbrodt
Silvio O Rizzoli
Silvio O Rizzoli
author_sort Sven eTruckenbrodt
title Spontaneous Vesicle Recycling in the Synaptic Bouton
title_short Spontaneous Vesicle Recycling in the Synaptic Bouton
title_full Spontaneous Vesicle Recycling in the Synaptic Bouton
title_fullStr Spontaneous Vesicle Recycling in the Synaptic Bouton
title_full_unstemmed Spontaneous Vesicle Recycling in the Synaptic Bouton
title_sort spontaneous vesicle recycling in the synaptic bouton
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2014-12-01
description The trigger for synaptic vesicle exocytosis is Ca2+, which enters the synaptic bouton following action potential stimulation. However, spontaneous release of neurotransmitter also occurs in the absence of stimulation in virtually all synaptic boutons. It has long been thought that this represents exocytosis driven by fluctuations in local Ca2+ levels. The vesicles responding to these fluctuations are thought to be the same ones that release upon stimulation, albeit potentially triggered by different Ca2+ sensors. This view has been challenged by several recent works, which have suggested that spontaneous release is driven by a separate pool of synaptic vesicles. Numerous articles appeared during the last few years in support of each of these hypotheses, and it has been challenging to bring them into accord. We speculate here on the origins of this controversy, and propose a solution that is related to developmental effects. Constitutive membrane traffic, needed for the biogenesis of vesicles and synapses, is responsible for high levels of spontaneous membrane fusion in young neurons, probably independent of Ca2+. The vesicles releasing spontaneously in such neurons are not related to other synaptic vesicle pools and may represent constitutively releasing vesicles (CRVs) rather than bona fide synaptic vesicles. In mature neurons, constitutive traffic is much dampened, and the few remaining spontaneous release events probably represent bona fide spontaneously releasing synaptic vesicles (SRSVs) responding to Ca2+ fluctuations, along with a handful of CRVs that participate in synaptic vesicle turnover.
topic synapse development
spontaneous release
synaptic vesicle pools
synaptic vesicle recycling
synaptic vesicle biogenesis
url http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00409/full
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