Abstract
The excitability of dopaminergic (DA) neurons in the substantia nigra is controlled by the convergent activity of multiple glutamatergic afferents. Here, we show that vesicular glutamate transporter 3 (VGLUT3)-immunoreactive (ir) terminals segregate to the perisomatic region of DA neurons in the substantia nigra pars compacta, and VGLUT3 decorates a synapse population distinct from those marked by vesicular glutamate transporters 1 and 2. VGLUT3-ir nerve endings form asymmetric terminals on DA neurons. Retrograde tracing suggests the superior colliculus as an origin of excitatory VGLUT3-ir afferents. Collectively, our data indicate that VGLUT3 identifies a novel excitatory terminal subset that contributes to the tuning of DA cell excitability in the substantia nigra.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Biotin / analogs & derivatives
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Biotin / metabolism
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Blotting, Western / methods
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Chromones
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Dextrans / metabolism
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Fluorescent Antibody Technique / methods
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Microscopy, Immunoelectron / methods
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Neurons / cytology*
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Neurons / metabolism
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Neurons / ultrastructure
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Phosphopyruvate Hydratase / metabolism
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Presynaptic Terminals / metabolism*
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Presynaptic Terminals / ultrastructure
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Rats
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Rats, Sprague-Dawley
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Receptor, Cannabinoid, CB1 / metabolism
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Serotonin / metabolism
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Substantia Nigra / cytology*
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Tyrosine 3-Monooxygenase / metabolism
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Vesicle-Associated Membrane Protein 2 / metabolism
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Vesicular Glutamate Transport Protein 2 / metabolism
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Vesicular Glutamate Transport Proteins / metabolism*
Substances
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5-hydroxy-2-(14'-nonadecenyl) chromone
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Chromones
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Dextrans
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Receptor, Cannabinoid, CB1
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Slc17a8 protein, rat
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Vesicle-Associated Membrane Protein 2
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Vesicular Glutamate Transport Protein 2
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Vesicular Glutamate Transport Proteins
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biotinylated dextran amine
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Serotonin
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Biotin
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Tyrosine 3-Monooxygenase
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Phosphopyruvate Hydratase