Abstract
Synaptic incorporation of NMDA receptors (NMDARs) is regulated by GluN2 subunits with different rules controlling GluN2A- and GluN2B-containing receptors; whereas GluN2B-containing receptors are constitutively incorporated into synapses, GluN2A incorporation is activity-dependent. We expressed electrophysiologically tagged NMDARs in rat hippocampal slices to identify the molecular determinants controlling the mode of synaptic incorporation of NMDARs. Expressing chimeric GluN2 subunits, we identified a putative N-glycosylation site present in GluN2B, but not in GluN2A, as necessary and sufficient to drive NMDARs into synapses in an activity-independent manner. This suggests a novel mechanism for regulating activity-driven changes and trafficking of NMDARs to the synapse.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Animals, Newborn
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Biophysics
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Electric Stimulation / methods
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Excitatory Amino Acid Antagonists / pharmacology
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Excitatory Postsynaptic Potentials / genetics
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Excitatory Postsynaptic Potentials / physiology
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Green Fluorescent Proteins / genetics
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Hippocampus / cytology*
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Macromolecular Substances / chemistry
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Male
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Mutation / genetics
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Neurons / physiology*
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Organ Culture Techniques
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Patch-Clamp Techniques / methods
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Protein Subunits
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Rats
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Rats, Sprague-Dawley
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Receptors, N-Methyl-D-Aspartate / chemistry
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Receptors, N-Methyl-D-Aspartate / genetics
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Receptors, N-Methyl-D-Aspartate / physiology*
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Synapses / physiology*
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Time Factors
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Transfection / methods
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Valine / analogs & derivatives
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Valine / pharmacology
Substances
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Excitatory Amino Acid Antagonists
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Macromolecular Substances
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NR2A NMDA receptor
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NR2B NMDA receptor
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Protein Subunits
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Receptors, N-Methyl-D-Aspartate
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Green Fluorescent Proteins
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2-amino-5-phosphopentanoic acid
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Valine