Cited by 268Amino Acid Enzymes and MetabolismBarrier Structure and Function StudiesNeuroscience and Neuropharmacology Research

Na+-dependent Glutamate Transporters (EAAT1, EAAT2, and EAAT3) of the Blood-Brain Barrier

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O'Kane, Robyn L., Martı́nez-López, Itziar, DeJoseph, Mary R., Viña, Juan R., Hawkins, Richard A.·1999·Journal of Biological Chemistry

Abstract

Na(+)-dependent transporters for glutamate exist on astrocytes (EAAT1 and EAAT2) and neurons (EAAT3). These transporters presumably assist in keeping the glutamate concentration low in the extracellular fluid of brain. Recently, Na(+)-dependent glutamate transport was described on the abluminal membrane of the blood-brain barrier. To determine whether the above-mentioned transporters participate in glutamate transport of the blood-brain barrier, total RNA was extracted from bovine cerebral capillaries. cDNA for EAAT1, EAAT2, and EAAT3 was observed, indicating that mRNA was present. Western blot analysis demonstrated all three transporters were expressed on abluminal membranes, but none was detectable on luminal membranes of the blood-brain barrier. Measurement of transport kinetics demonstrated voltage dependence, K(+)-dependence, and an apparent K(m) of 14 microM (aggregate of the three transporters) at a transmembrane potential of -61 mV. Inhibition of glutamate transport was observed using inhibitors specific for EAAT2 (kainic acid and dihydrokainic acid) and EAAT3 (cysteine). The relative activity of the three transporters was found to be approximately 1:3:6 for EAAT1, EAAT2, and EAAT3, respectively. These transporters may assist in maintaining low glutamate concentrations in the extracellular fluid.

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Crossref · 10.1074/jbc.274.45.31891

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  • On the abluminal endothelial membrane, sodium-dependent transporters for excitatory amino acids (EAAT1/2/3) transport glutamate and aspartate out of the brain.

    “On the abluminal endothelial membrane, sodium-dependent transporters for excitatory AA (EAAT1/2/3) transport glutamate and aspartate out of the brain (451, 692), which limits their excitotoxic effects on neurons.”

    From Blood-Brain Barrier: From Physiology to Disease and Back (2019) · cites this paper as [451]

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References 47 · Cited by 268

Authors
O'Kane, R. L., Martı́nez-López, I., DeJoseph, M. R., Viña, J. R., & Hawkins, R. A.
Affiliations
Universitat de València (ES)
Corresponding author
Hawkins, Richard A.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1999-11
Volume
274
Issue
45
Pages
31891-31895
ISSN
0021-9258 (ISSN-L)
OpenAlex
W2078517229
Cited by
268
References
47
Citations by year
2026: 1 · 2025: 3 · 2024: 7 · 2023: 7 · 2022: 13 · 2021: 11 · 2020: 9 · 2019: 6 · 2018: 13 · 2017: 9 · 2016: 14 · 2015: 13 · 2014: 11 · 2013: 17 · 2012: 17
FWCI
3.20
Type
journal article
Language
en
Open access
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ns031017-03)
  • National Institute of Neurological Disorders and Stroke (NS-31017)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
  • Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
GLAST, GLT-1, EAAT3, blood-brain barrier, cerebral microvasculature, kainic acid, dihydrokainic acid, cysteine, voltage dependence, transporter expression
MeSH terms
Animals, Biological Transport, Blood-Brain Barrier, Carrier Proteins, Cattle, Kinetics, Models, Biological, Receptors, Neurotransmitter, ATP-Binding Cassette Transporters, Glutamic Acid, Amino Acid Transport System X-AG, Excitatory Amino Acid Transporter 2, Symporters, Glutamate Plasma Membrane Transport Proteins

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