Abstract
Excitatory amino-acid transporters (EAATs) in the central nervous system maintain extracellular glutamate concentrations below excitotoxic levels and may limit the activation of glutamate receptors. Here we report the cloning of a novel human aspartate/glutamate transporter, EAAT4, which is expressed predominantly in the cerebellum. The transport activity encoded by EAAT4 has high apparent affinity for L-aspartate and L-glutamate, and has a pharmacological profile consistent with previously described cerebellar transport activities. In Xenopus oocytes expressing EAAT4, L-aspartate and L-glutamate elicited a current predominantly carried by chloride ions. This chloride conductance was not blocked by components that block endogenous oocyte chloride channels. Thus EAAT4 combines the re-uptake of neurotransmitter with a mechanism for increasing chloride permeability, both of which could regulate excitatory neurotransmission.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Amino Acid Sequence
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Amino Acid Transport System X-AG*
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Animals
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Aspartic Acid / metabolism
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Base Sequence
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Cells, Cultured
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Cerebellum / metabolism*
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Chloride Channels / genetics
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Chloride Channels / metabolism*
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Chlorides / metabolism
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DNA, Complementary
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Excitatory Amino Acid Transporter 4
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Glutamate Plasma Membrane Transport Proteins
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Humans
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Ion Channel Gating
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Ligands
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Membrane Potentials
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Molecular Sequence Data
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Oocytes / metabolism
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Receptors, Amino Acid / genetics
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Receptors, Amino Acid / metabolism*
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Receptors, Glutamate / genetics
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Receptors, Glutamate / metabolism*
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Sequence Homology, Amino Acid
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Sodium / metabolism
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Symporters*
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Xenopus
Substances
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Amino Acid Transport System X-AG
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Chloride Channels
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Chlorides
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DNA, Complementary
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Excitatory Amino Acid Transporter 4
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Glutamate Plasma Membrane Transport Proteins
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Ligands
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Receptors, Amino Acid
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Receptors, Glutamate
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SLC1A6 protein, human
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Symporters
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aspartic acid receptor
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Aspartic Acid
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Sodium