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      Fluorescent false neurotransmitter reveals functionally silent dopamine vesicle clusters in the striatum

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          Abstract

          Neurotransmission at dopaminergic synapses has been studied with techniques that provide high temporal resolution but cannot resolve individual synapses. To elucidate the spatial dynamics and heterogeneity of individual dopamine boutons, we developed fluorescent false neurotransmitter 200 (FFN200), a vesicular monoamine transporter 2 (VMAT2) substrate that is the first probe to selectively trace monoamine exocytosis in both neuronal cell culture and brain tissue. By monitoring electrically-evoked Ca 2+ transients with GCaMP3 and FFN200 release simultaneously, we find that only a small fraction of dopamine boutons that exhibit Ca 2+ influx engage in exocytosis, a result confirmed with activity-dependent loading of the endocytic probe FM 1-43. Thus, only a low fraction of striatal dopamine axonal sites with uptake-competent VMAT2 vesicles are capable of transmitter release. This is consistent with the presence of functionally “silent” dopamine vesicle clusters and represents a first report suggestive of presynaptically silent neuromodulatory synapses.

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          Most cited references50

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          Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system.

          alpha-Synuclein (alpha-Syn) is a 14 kDa protein of unknown function that has been implicated in the pathophysiology of Parkinson's disease (PD). Here, we show that alpha-Syn-/- mice are viable and fertile, exhibit intact brain architecture, and possess a normal complement of dopaminergic cell bodies, fibers, and synapses. Nigrostriatal terminals of alpha-Syn-/- mice display a standard pattern of dopamine (DA) discharge and reuptake in response to simple electrical stimulation. However, they exhibit an increased release with paired stimuli that can be mimicked by elevated Ca2+. Concurrent with the altered DA release, alpha-Syn-/- mice display a reduction in striatal DA and an attenuation of DA-dependent locomotor response to amphetamine. These findings support the hypothesis that alpha-Syn is an essential presynaptic, activity-dependent negative regulator of DA neurotransmission.
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            The control of firing pattern in nigral dopamine neurons: burst firing.

            In addition to firing in a single spiking mode, dopamine (DA) cells have been observed to fire in a bursting pattern with consecutive spikes in a burst displaying progressively decreasing amplitude and increasing duration. In vivo intracellular recording demonstrated the bursts to typically ride on a depolarizing wave (5 to 15 mV amplitude). Although the burst-firing frequency of DA cells showed little correlation with the base line firing rate, increases in firing rate were usually associated with an increase in burst firing. Increases in burst firing could also be elicited by intracellular calcium injection and could be prevented by intracellular injection of EGTA, suggesting a calcium involvement in bursting. Blockade of potassium conductances with extracellular iontophoresis of barium or intracellular injection of tetraethylammonium bromide could also trigger an increased degree of burst firing in DA cells. These data suggest that the increased calcium influx accompanying an increased firing rate triggers burst firing, possibly by inactivating a potassium conductance. A switch from a single spiking mode to a burst-firing mode may be important in modulating striatal DA release, as shown for burst firing in other preparations.
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              Characterization of a mouse strain expressing Cre recombinase from the 3' untranslated region of the dopamine transporter locus.

              Dopamine (DA) neurotransmission has been implicated in several neurological and psychiatric disorders. The dopamine transporter (DAT) is highly expressed in dopaminergic neurons of the ventral mesencephalon and regulates neurotransmission by transporting DA back into the presynaptic terminals. To mediate restricted DNA recombination events into DA neurons using the Cre/loxP technology, we have generated a knockin mouse expressing Cre recombinase under the transcriptional control of the endogenous DAT promoter. To minimize interference with DAT function by preservation of both DAT alleles, Cre recombinase expression was driven from the 3' untranslated region (3'UTR) of the endogenous DAT gene by means of an internal ribosomal entry sequence. Crossing this murine line with a LacZ reporter showed colocalization of DAT immunocytochemistry and beta-galactosidase staining in all regions analyzed. This knockin mouse can be used for generating tissue specific knockouts in mice carrying genes flanked by loxP sites, and will facilitate the analysis of gene function in dopaminergic neurons. Copyright 2006 Wiley-Liss, Inc.
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                Author and article information

                Journal
                9809671
                21092
                Nat Neurosci
                Nat. Neurosci.
                Nature neuroscience
                1097-6256
                1546-1726
                12 February 2016
                22 February 2016
                April 2016
                22 August 2016
                : 19
                : 4
                : 578-586
                Affiliations
                [1 ]Department of Neurology, Columbia University Medical Center, New York, NY
                [2 ]Department of Psychiatry, Columbia University Medical Center, New York, NY
                [3 ]Department of Pharmacology, Columbia University Medical Center, New York, NY
                [4 ]Department of Neuroscience, New York Psychiatric Institute, New York, NY
                [5 ]Department of Chemistry, Columbia University, New York, NY
                Author notes
                Corresponding Authors: David Sulzer, Columbia University Medical Center, 650 West 168 th Street BB308, New York, NY 10032, ds43@ 123456cumc.columbia.edu and Dalibor Sames, Columbia University, 3000 Broadway, MC3101, New York, NY 10027, ds584@ 123456columbia.edu , and Daniela B. Pereira, Champalimaud Neuroscience Program, Champalimaud Center for the Unknown, Av. De Brasília, Doca de Pedrouços, 1400-038 Lisbon, Portugal, nydp2003@ 123456gmail.com
                [6]

                current address: Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Lisbon, Portugal.

                [7]

                current address: Infineum USA L.P., Linden, NJ.

                [8]

                current address: Pharmasan Labs. Inc., Osceola, WI.

                [9]

                current address: California Institute for Biomedical Research, La Jolla, CA.

                [10]

                current address: Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Perelman School of Medicine, University of Pennsylvania, PA.

                [11]

                current address: Institute of Biology, École Normale Supérieure, Paris, France.

                [12]

                co-corresponding authors

                Article
                NIHMS754393
                10.1038/nn.4252
                4853199
                26900925
                947188a9-1a15-4eb9-a9e0-6a1dce47d1cc

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