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The Regulation of Astrocytic Glutamate Transporters in Health and Neurodegenerative Diseases
Abstract
The astrocytic glutamate transporters excitatory amino acid transporters 1 and 2 (EAAT1 and EAAT2) play a key role in nervous system function to maintain extracellular glutamate levels at low levels. In physiology, this is essential for the rapid uptake of synaptically released glutamate, maintaining the temporal fidelity of synaptic transmission. However, EAAT1/2 hypo-expression or hypo-function are implicated in several disorders, including epilepsy and neurodegenerative diseases, as well as being observed naturally with aging. This not only disrupts synaptic information transmission, but in extremis leads to extracellular glutamate accumulation and excitotoxicity. A key facet of EAAT1/2 expression in astrocytes is a requirement for signals from other brain cell types in order to maintain their expression. Recent evidence has shown a prominent role for contact-dependent neuron-to-astrocyte and/or endothelial cell-to-astrocyte Notch signalling for inducing and maintaining the expression of these astrocytic glutamate transporters. The relevance of this non-cell-autonomous dependence to age- and neurodegenerative disease-associated decline in astrocytic EAAT expression is discussed, plus the implications for disease progression and putative therapeutic strategies.
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Excitotoxicity has been associated with several neurodegenerative disorders as well as epilepsy.
“Excitotoxicity has been associated with several neurodegenerative disorders as well as epilepsy [124,125].”
From Global identification of neuronal and astrocytic integral membrane proteins that require Retromer for their endosomal recycling (2026) · cites this paper as [124]
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Rosen, D. R., Siddique, T., Patterson, D., Figlewicz, D. A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J. P., Deng, H.-X., et al. (1993) · Nature · doi:10.1038/362059a0 · Cited by 7,062
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129 · cited 1×
“This is consistent with the observation that in astrocytes 22 isolated ex vivo both EAAT1/2 expression and notch target genes decline in culture compared to their 23 levels immediately post-isolation [101, 127].”
ResultSynaptic versus extrasynaptic NMDA receptor signalling: implications for neurodegenerative disorders
Hardingham, G. E., & Bading, H. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2911 · Cited by 1,644 · cited 1×
“33 Significantly, if glutamate escapes the synaptic region it can activate extrasynaptic NMDA receptors: 34 too much Ca2+ influx via these extrasynaptic NMDA receptors induces signalling cascades that 35 initiate cell death programs [2, 3].”
BackgroundSelf-citationHomeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function
Turrigiano, G. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005736 · Cited by 1,139 · cited 1×
“[138-141], although direct evidence so far extends to Hebbian, spike timing14 dependent plasticity [142].”
BackgroundTrophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture
Banker, G. A. (1980) · Science · doi:10.1126/science.7403847 · Cited by 674
Deficient glutamate tranport is associated with neurodegeneration in Alzheimer's disease
Masliah, E., Hansen, L., Alford, M., Deteresa, R., & Mallory, M. (1996) · Annals of Neurology · doi:10.1002/ana.410400512 · Cited by 476
The SLC1 high-affinity glutamate and neutral amino acid transporter family
Kanai, Y., Clémençon, B., Simonin, A., Leuenberger, M., Lochner, M., Weisstanner, M., & Hediger, M. A. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2013.01.001 · Cited by 329
Jacob, C. P., Koutsilieri, E., Bartl, J., Neuen-Jacob, E., Arzberger, T., Zander, N., Ravid, R., Roggendorf, W., Riederer, P., & Grünblatt, E. (2007) · Journal of Alzheimer's Disease · doi:10.3233/jad-2007-11113 · Cited by 317
Petr, G. T., Sun, Y., Frederick, N. M., Zhou, Y., Dhamne, S. C., Hameed, M. Q., Miranda, C., Bedoya, E. A., Fischer, K. D., Armsen, W., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4255-14.2015 · Cited by 297
Lessons from a failed γ-secretase Alzheimer trial
De Strooper, B. (2014) · Cell · doi:10.1016/j.cell.2014.10.016 · Cited by 277
Surface diffusion of astrocytic glutamate transporters shapes synaptic transmission
Murphy-Royal, C., Dupuis, J. P., Varela, J. A., Panatier, A., Pinson, B., Baufreton, J., Groc, L., & Oliet, S. H. R. (2015) · Nature Neuroscience · doi:10.1038/nn.3901 · Cited by 252
Amyloid-β 1–42 Slows Clearance of Synaptically Released Glutamate by Mislocalizing Astrocytic GLT-1
Scimemi, A., Meabon, J. S., Woltjer, R. L., Sullivan, J. M., Diamond, J. S., & Cook, D. G. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5274-12.2013 · Cited by 185
A multiregional proteomic survey of the postnatal human brain
Carlyle, B. C., Kitchen, R. R., Kanyo, J. E., Voss, E. Z., Pletikos, M., Sousa, A. M. M., Lam, T. T., Gerstein, M. B., Sestan, N., & Nairn, A. C. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0011-2 · Cited by 143
Synaptic NMDA receptor activity is coupled to the transcriptional control of the glutathione system
Baxter, P. S., Bell, K. F. S., Hasel, P., Kaindl, A. M., Fricker, M., Thomson, D., Cregan, S. P., Gillingwater, T. H., & Hardingham, G. E. (2015) · Nature Communications · doi:10.1038/ncomms7761 · Cited by 139
Self-citationAge and Alzheimer’s disease gene expression profiles reversed by the glutamate modulator riluzole
Pereira, A. C., Gray, J. D., Kogan, J. F., Davidson, R. L., Rubin, T. G., Okamoto, M., Morrison, J. H., & McEwen, B. S. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.33 · Cited by 116
Higashimori, H., Schin, C. S., Chiang, M. S. R., Morel, L., Shoneye, T. A., Nelson, D. L., & Yang, Y. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1069-16.2016 · Cited by 105
Lewerenz, J., Baxter, P., Kassubek, R., Albrecht, P., Van Liefferinge, J., Westhoff, M.-A., Halatsch, M.-E., Karpel-Massler, G., Meakin, P. J., Hayes, J. D., et al. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5455 · Cited by 66
Self-citationHardingham, N. R., Read, J. C. A., Trevelyan, A. J., Nelson, J. C., Jack, J. J. B., & Bannister, N. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3244-09.2010 · Cited by 57
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease
Ferrarese, C., Tremolizzo, L., Rigoldi, M., Sala, G., Brighina, L., Ricci, G., Albizzati, M. G., Piolti, R., Crosti, F., Dalpr�, L., et al. (2001) · Neurological Sciences · doi:10.1007/s100720170049 · Cited by 39
Flagged first, then by citations
Research works printed but not linked: 216
- Danbolt, 2001, Glutamate uptake, Prog. Neurobiol., 65, 1, 10.1016/S0301-0082(00)00067-8 · DOI · Paper page
- Wahl, 2009, Hypoxic/ischemic conditions induce expression of the putative pro-death gene Clca1 via activation of extrasynaptic N-methyl-d-aspartate receptors, Neuroscience, 158, 344, 10.1016/j.neuroscience.2008.06.018 · DOI
- Lindsay, 1979, Adult rat brain astrocytes support survival of both NGF-dependent and NGF-insensitive neurones, Nat. Cell Biol., 282, 80
- Rosenberg, 1992, Glutamate uptake disguises neurotoxic potency of glutamate agonists in cerebral cortex in dissociated cell culture, J. Neurosci., 12, 56, 10.1523/JNEUROSCI.12-01-00056.1992 · DOI
- Rosenberg, 1989, Hundred-fold increase in neuronal vulnerability to glutamate toxicity in astrocyte-poor cultures of rat cerebral cortex, Neurosci. Lett., 103, 162, 10.1016/0304-3940(89)90569-7 · DOI
- Hardingham, 2011, Regulation of Neuronal Oxidative and Nitrosative Stress by Endogenous Protective Pathways and Disease Processes, Antioxid. Redox Signal., 14, 1421, 10.1089/ars.2010.3573 · DOI
- Gupta, 2013, NMDA receptor-dependent glutamate excitotoxicity in human embryonic stem cell-derived neurons, Neurosci. Lett., 543, 95, 10.1016/j.neulet.2013.03.010 · DOI
- Hertz, 2014, Astrocytic—Neuronal—Astrocytic Pathway Selection for Formation and Degradation of Glutamate/GABA, Front. Endocrinol., 5, 5, 10.3389/fendo.2014.00042 · DOI
- Schousboe, A., and Sonnewald, U. (2016). Introduction to the Glutamate–Glutamine Cycle. The Glutamate/GABA-Glutamine Cycle: Amino Acid Neurotransmitter Homeostasis, Springer International Publishing. · DOI
- Billups, 2013, Inducible Presynaptic Glutamine Transport Supports Glutamatergic Transmission at the Calyx of Held Synapse, J. Neurosci., 33, 17429, 10.1523/JNEUROSCI.1466-13.2013 · DOI
- Tani, 2014, A Local Glutamate-Glutamine Cycle Sustains Synaptic Excitatory Transmitter Release, Neuron, 81, 888, 10.1016/j.neuron.2013.12.026 · DOI
- Todd, 2017, SNAT3-mediated glutamine transport in perisynaptic astrocytesin situis regulated by intracellular sodium, Glia, 65, 900, 10.1002/glia.23133 · DOI
- Uwechue, 2012, Activation of glutamate transport evokes rapid glutamine release from perisynaptic astrocytes, J. Physiol., 590, 2317, 10.1113/jphysiol.2011.226605 · DOI
- Freidman, 2020, Amino Acid Transporters and Exchangers from the SLC1A Family: Structure, Mechanism and Roles in Physiology and Cancer, Neurochem. Res., 45, 1268, 10.1007/s11064-019-02934-x · DOI
- Grewer, 2013, SLC1 glutamate transporters, Pflügers Arch. Eur. J. Physiol., 466, 3, 10.1007/s00424-013-1397-7 · DOI
- Verkhratsky, A., Ho, M.S., Zorec, R., and Parpura, V. (2019). Physiology of Astroglia. Neuroglia in Neurodegenerative Diseases, Springer. · DOI
- Wirth, 2013, Effects of age and sex on the concentrations of glutamate and glutamine in the human brain, J. Magn. Reson. Imaging, 38, 1480, 10.1002/jmri.24123 · DOI
- Schubert, 2004, Glutamate concentrations in human brain using single voxel proton magnetic resonance spectroscopy at 3 Tesla, NeuroImage, 21, 1762, 10.1016/j.neuroimage.2003.11.014 · DOI
- Lehmann, 1983, Effects of In Vivo Administration of Kainic Acid on the Extracellular Amino Acid Pool in the Rabbit Hippocampus, J. Neurochem., 40, 1314, 10.1111/j.1471-4159.1983.tb13572.x · DOI
- Hamberger, 1984, Extra- and intracellular amino acids in the hippocampus during development of hepatic encephalopathy, Neurochem. Res., 9, 1181, 10.1007/BF00973033 · DOI
- Erecinska, 1990, Metabolism and role of glutamate in mammalian brain, Prog. Neurobiol., 35, 245, 10.1016/0301-0082(90)90013-7 · DOI
- Ortega, A., and Schousboe, A. (2017). Glutamate Transporters in the Blood-Brain Barrier. Advances in Neurobiology, Springer International Publishing. · DOI
- Fotiadis, 2013, The SLC3 and SLC7 families of amino acid transporters, Mol. Asp. Med., 34, 139, 10.1016/j.mam.2012.10.007 · DOI
- Bridges, 2011, System xc- cystine/glutamate antiporter: An update on molecular pharmacology and roles within the CNS, Br. J. Pharmacol., 165, 20, 10.1111/j.1476-5381.2011.01480.x · DOI
- Hu, 2018, The cystine-glutamate exchanger (xCT, Slc7a11) is expressed in significant concentrations in a subpopulation of astrocytes in the mouse brain, Glia, 66, 951, 10.1002/glia.23294 · DOI
- Logan, 1971, Unique High Affinity Uptake Systems for Glycine, Glutamic and Aspartic Acids in Central Nervous Tissue of the Rat, Nature, 234, 297, 10.1038/234297b0 · DOI
- Balcar, 1972, The Structural Specificity of the High Affinity Uptake of l-glutamate and l-Aspartate by Rat Brain Slices, J. Neurochem., 19, 2657, 10.1111/j.1471-4159.1972.tb01325.x · DOI
- Kanai, 1992, Primary structure and functional characterization of a high-affinity glutamate transporter, Nature, 360, 467, 10.1038/360467a0 · DOI
- Pines, 1992, Cloning and expression of a rat brain l-glutamate transporter, Nature, 360, 464, 10.1038/360464a0 · DOI
- Storck, 1992, Structure, expression, and functional analysis of a Na(+)-dependent glutamate/aspartate transporter from rat brain, Proc. Natl. Acad. Sci. USA, 89, 10955, 10.1073/pnas.89.22.10955 · DOI
- Balcar, 1977, High affinity uptake of l-glutamate and l-Aspartate by glial cells, J. Neurochem., 28, 87, 10.1111/j.1471-4159.1977.tb07712.x · DOI
- Tanaka, 1993, Cloning and expression of a glutamate transporter from mouse brain, Neurosci. Lett., 159, 183, 10.1016/0304-3940(93)90829-A · DOI
- Fairman, 1995, An excitatory amino-acid transporter with properties of a ligand-gated chloride channel, Nature, 375, 599, 10.1038/375599a0 · DOI
- Arriza, 1997, Excitatory amino acid transporter 5, a retinal glutamate transporter coupled to a chloride conductance, Proc. Natl. Acad. Sci. USA, 94, 4155, 10.1073/pnas.94.8.4155 · DOI
- Arriza, 1994, Functional comparisons of three glutamate transporter subtypes cloned from human motor cortex, J. Neurosci., 14, 5559, 10.1523/JNEUROSCI.14-09-05559.1994 · DOI
- Wadiche, 1998, Macroscopic and Microscopic Properties of a Cloned Glutamate Transporter/Chloride Channel, J. Neurosci., 18, 7650, 10.1523/JNEUROSCI.18-19-07650.1998 · DOI
- Wadiche, 1995, Ion fluxes associated with excitatory amino acid transport, Neuron, 15, 721, 10.1016/0896-6273(95)90159-0 · DOI
- Jensen, 2004, Pharmacological characterization of human excitatory amino acid transporters EAAT1, EAAT2 and EAAT3 in a fluorescence-based membrane potential assay, Biochem. Pharmacol., 67, 2115, 10.1016/j.bcp.2004.02.013 · DOI
- Grewer, 2000, Glutamate translocation of the neuronal glutamate transporter EAAC1 occurs within milliseconds, Proc. Natl. Acad. Sci. USA, 97, 9706, 10.1073/pnas.160170397 · DOI
- Gameiro, 2011, The Discovery of Slowness: Low-Capacity Transport and Slow Anion Channel Gating by the Glutamate Transporter EAAT5, Biophys. J., 100, 2623, 10.1016/j.bpj.2011.04.034 · DOI
- Mim, 2005, The Glutamate Transporter Subtypes EAAT4 and EAATs 1-3 Transport Glutamate with Dramatically Different Kinetics and Voltage Dependence but Share a Common Uptake Mechanism, J. Gen. Physiol., 126, 571, 10.1085/jgp.200509365 · DOI
- Bellocchio, 2000, Uptake of Glutamate into Synaptic Vesicles by an Inorganic Phosphate Transporter, Science, 289, 957, 10.1126/science.289.5481.957 · DOI
- Herzog, 2001, The Existence of a Second Vesicular Glutamate Transporter Specifies Subpopulations of Glutamatergic Neurons, J. Neurosci., 21, RC181, 10.1523/JNEUROSCI.21-22-j0001.2001 · DOI
- Fremeau, 2002, The identification of vesicular glutamate transporter 3 suggests novel modes of signaling by glutamate, Proc. Natl. Acad. Sci. USA, 99, 14488, 10.1073/pnas.222546799 · DOI
- Patel, 2004, Differentiation of substrate and non-substrate inhibitors of transport system xc−: An obligate exchanger of l-glutamate and L-cystine, Neuropharmacology, 46, 273, 10.1016/j.neuropharm.2003.08.006 · DOI
- Seib, 2011, Regulation of the System x−C cystine/glutamate exchanger by intracellular glutathione levels in rat astrocyte primary cultures, Glia, 59, 1387, 10.1002/glia.21176 · DOI
- Sheehan, 2016, Neuronal activity mediated regulation of glutamate transporter GLT-1 surface diffusion in rat astrocytes in dissociated and slice cultures, Glia, 64, 1252, 10.1002/glia.22997 · DOI
- Sultana, 2015, GLAST But Not Least—Distribution, Function, Genetics and Epigenetics of l-glutamate Transport in Brain—Focus on GLAST/EAAT1, Neurochem. Res., 40, 2461, 10.1007/s11064-015-1605-2 · DOI
- Zhou, 2013, GABA and Glutamate Transporters in Brain, Front. Endocrinol., 4, 165, 10.3389/fendo.2013.00165 · DOI
- Chaudhry, 1995, Glutamate transporters in glial plasma membranes: Highly differentiated localizations revealed by quantitative ultrastructural immunocytochemistry, Neuron, 15, 711, 10.1016/0896-6273(95)90158-2 · DOI
- Lehre, 1998, The Number of Glutamate Transporter Subtype Molecules at Glutamatergic Synapses: Chemical and Stereological Quantification in Young Adult Rat Brain, J. Neurosci., 18, 8751, 10.1523/JNEUROSCI.18-21-08751.1998 · DOI
- Lehre, 1995, Differential expression of two glial glutamate transporters in the rat brain: Quantitative and immunocytochemical observations, J. Neurosci., 15, 1835, 10.1523/JNEUROSCI.15-03-01835.1995 · DOI
- Schmitt, 1997, Cellular and Regional Distribution of the Glutamate Transporter GLAST in the CNS of Rats: Nonradioactive In Situ Hybridization and Comparative Immunocytochemistry, J. Neurosci., 17, 1, 10.1523/JNEUROSCI.17-01-00001.1997 · DOI
- Rothstein, 1994, Localization of neuronal and glial glutamate transporters, Neuron, 13, 713, 10.1016/0896-6273(94)90038-8 · DOI
- Derouiche, 1995, Coincidence of l-glutamate/l-Aspartate transporter (GLAST) and glutamine synthetase (GS) immunoreactions in retinal glia: Evidence for coupling of GLAST and GS in transmitter clearance, J. Neurosci. Res., 42, 131, 10.1002/jnr.490420115 · DOI
- Lehre, 1997, Localization of the glutamate transporter protein GLAST in rat retina, Brain Res., 744, 129, 10.1016/S0006-8993(96)01022-0 · DOI
- Pow, 1999, Changing patterns of spatial buffering of glutamate in developing rat retinae are mediated by the Müller cell glutamate transporter GLAST, Cell Tissue Res., 297, 57, 10.1007/s004410051333 · DOI
- Rose, 2018, Molecular and cellular physiology of sodium-dependent glutamate transporters, Brain Res. Bull., 136, 3, 10.1016/j.brainresbull.2016.12.013 · DOI
- Holmseth, 2012, The Density of EAAC1 (EAAT3) Glutamate Transporters Expressed by Neurons in the Mammalian CNS, J. Neurosci., 32, 6000, 10.1523/JNEUROSCI.5347-11.2012 · DOI
- Shashidharan, 1997, Immunohistochemical localization of the neuron-specific glutamate transporter EAAC1 (EAAT3) in rat brain and spinal cord revealed by a novel monoclonal antibody, Brain Res., 773, 139, 10.1016/S0006-8993(97)00921-9 · DOI
- Dehnes, 1998, The Glutamate Transporter EAAT4 in Rat Cerebellar Purkinje Cells: A Glutamate-Gated Chloride Channel Concentrated near the Synapse in Parts of the Dendritic Membrane Facing Astroglia, J. Neurosci., 18, 3606, 10.1523/JNEUROSCI.18-10-03606.1998 · DOI
- Massie, 2008, High-affinity Na+/K+-dependent glutamate transporter EAAT4 is expressed throughout the rat fore- and midbrain, J. Comp. Neurol., 511, 155, 10.1002/cne.21823 · DOI
- Pow, 2000, Developmental expression of excitatory amino acid transporter 5: A photoreceptor and bipolar cell glutamate transporter in rat retina, Neurosci. Lett., 280, 21, 10.1016/S0304-3940(99)00988-X · DOI
- Eliasof, 1998, Excitatory Amino Acid Transporters of the Salamander Retina: Identification, Localization, and Function, J. Neurosci., 18, 698, 10.1523/JNEUROSCI.18-02-00698.1998 · DOI
- Wersinger, 2006, The glutamate transporter EAAT5 works as a presynaptic receptor in mouse rod bipolar cells, J. Physiol., 577, 221, 10.1113/jphysiol.2006.118281 · DOI
- Gegelashvili, 1998, Cellular Distribution and Kinetic Properties of High-Affinity Glutamate Transporters, Brain Res. Bull., 45, 233, 10.1016/S0361-9230(97)00417-6 · DOI
- Levy, 1998, Stoichiometry of the Glial Glutamate Transporter GLT-1 Expressed Inducibly in a Chinese Hamster Ovary Cell Line Selected for Low Endogenous Na+-Dependent Glutamate Uptake, J. Neurosci., 18, 9620, 10.1523/JNEUROSCI.18-23-09620.1998 · DOI
- Zerangue, 1996, Flux coupling in a neuronal glutamate transporter, Nature, 383, 634, 10.1038/383634a0 · DOI
- Kanai, 1995, Electrogenic Properties of the Epithelial and Neuronal High Affinity Glutamate Transporter, J. Biol. Chem., 270, 16561, 10.1074/jbc.270.28.16561 · DOI
- Yernool, 2004, Structure of a glutamate transporter homologue from Pyrococcus horikoshii, Nature, 431, 811, 10.1038/nature03018 · DOI
- Jensen, 2013, Crystal structure of a substrate-free aspartate transporter, Nat. Struct. Mol. Biol., 20, 1224, 10.1038/nsmb.2663 · DOI
- Arkhipova, V., Trinco, G., Ettema, T.W., Jensen, S., Slotboom, D.J., and Guskov, A. (2019). Binding and transport of D-aspartate by the glutamate transporter homolog GltTk. eLife, 8. · DOI
- Kortzak, 2019, Allosteric gate modulation confers K + coupling in glutamate transporters, EMBO J., 38, e101468, 10.15252/embj.2019101468 · DOI
- Brew, 1987, Electrogenic glutamate uptake is a major current carrier in the membrane of axolotl retinal glial cells, Nature, 327, 707, 10.1038/327707a0 · DOI
- Vandenberg, 1995, Constitutive Ion Fluxes and Substrate Binding Domains of Human Glutamate Transporters, J. Biol. Chem., 270, 17668, 10.1074/jbc.270.30.17668 · DOI
- Wyllie, 1991, Activation of glutamate receptors and glutamate uptake in identified macroglial cells in rat cerebellar cultures, J. Physiol., 432, 235, 10.1113/jphysiol.1991.sp018383 · DOI
- Machtens, 2015, Mechanisms of Anion Conduction by Coupled Glutamate Transporters, Cell, 160, 542, 10.1016/j.cell.2014.12.035 · DOI
- Fahlke, 2016, Molecular physiology of EAAT anion channels, Pflügers Arch. Eur. J. Physiol., 468, 491, 10.1007/s00424-015-1768-3 · DOI
- Schneider, 2013, Functional Properties of the Retinal Glutamate Transporters GLT-1c and EAAT, J. Biol. Chem., 289, 1815, 10.1074/jbc.M113.517177 · DOI
- Tse, 2014, Possible roles of glutamate transporter EAAT5 in mouse cone depolarizing bipolar cell light responses, Vis. Res., 103, 63, 10.1016/j.visres.2014.06.005 · DOI
- McLennan, 1976, The autoradiographic localization of L-[3H]glutamate in rat brain tissue, Brain Res., 115, 139, 10.1016/0006-8993(76)90828-3 · DOI
- Wilkin, 1982, Putative acidic amino acid transmitters in the cerebellum. II. Electron microscopic localization of transport sites, Brain Res., 244, 69, 10.1016/0006-8993(82)90905-2 · DOI
- Bergles, 1998, Glial Contribution to Glutamate Uptake at Schaffer Collateral–Commissural Synapses in the Hippocampus, J. Neurosci., 18, 7709, 10.1523/JNEUROSCI.18-19-07709.1998 · DOI
- Bergles, 1997, Synaptic Activation of Glutamate Transporters in Hippocampal Astrocytes, Neuron, 19, 1297, 10.1016/S0896-6273(00)80420-1 · DOI
- Tanaka, 1997, Epilepsy and Exacerbation of Brain Injury in Mice Lacking the Glutamate Transporter GLT-1, Science, 276, 1699, 10.1126/science.276.5319.1699 · DOI
- Watase, 1998, Motor discoordination and increased susceptibility to cerebellar injury in GLAST mutant mice, Eur. J. Neurosci., 10, 976, 10.1046/j.1460-9568.1998.00108.x · DOI
- Matsugami, 2006, Indispensability of the glutamate transporters GLAST and GLT1 to brain development, Proc. Natl. Acad. Sci. USA, 103, 12161, 10.1073/pnas.0509144103 · DOI
- Peghini, 1997, Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration, EMBO J., 16, 3822, 10.1093/emboj/16.13.3822 · DOI
- Drejer, 1983, Novel neuron-related regulatory mechanisms for astrocytic glutamate and GABA high affinity uptake, Neurosci. Lett., 37, 301, 10.1016/0304-3940(83)90448-2 · DOI
- Levy, 1995, Down-regulation of Glial Glutamate Transporters after Glutamatergic Denervation in the Rat Brain, Eur. J. Neurosci., 7, 2036, 10.1111/j.1460-9568.1995.tb00626.x · DOI
- Gegelashvili, 1996, Glutamate receptor agonists up-regulate glutamate transporter GLAST in astrocytes, NeuroReport, 8, 261, 10.1097/00001756-199612200-00052 · DOI
- Swanson, 1997, Neuronal Regulation of Glutamate Transporter Subtype Expression in Astrocytes, J. Neurosci., 17, 932, 10.1523/JNEUROSCI.17-03-00932.1997 · DOI
- Gegelashvili, 1997, Neuronal soluble factors differentially regulate the expression of the GLT1 and GLAST glutamate transporters in cultured astroglia, J. Neurochem., 69, 2612, 10.1046/j.1471-4159.1997.69062612.x · DOI
- Hasel, 2017, Neurons and neuronal activity control gene expression in astrocytes to regulate their development and metabolism, Nat. Commun., 8, 15132, 10.1038/ncomms15132 · DOI
- Schlag, 1998, Regulation of the Glial Na+-Dependent Glutamate Transporters by Cyclic AMP Analogs and Neurons, Mol. Pharmacol., 53, 355, 10.1124/mol.53.3.355 · DOI · Paper page
- Zelenaia, 2000, Epidermal Growth Factor Receptor Agonists Increase Expression of Glutamate Transporter GLT-1 in Astrocytes through Pathways Dependent on Phosphatidylinositol 3-Kinase and Transcription Factor NF-κB, Mol. Pharmacol., 57, 667, 10.1124/mol.57.4.667 · DOI
- Ghosh, 2011, Nuclear Factor- B Contributes to Neuron-Dependent Induction of Glutamate Transporter-1 Expression in Astrocytes, J. Neurosci., 31, 9159, 10.1523/JNEUROSCI.0302-11.2011 · DOI
- Sitcheran, 2005, Positive and negative regulation of EAAT2 by NF-κB: A role for N-myc in TNFα-controlled repression, EMBO J., 24, 510, 10.1038/sj.emboj.7600555 · DOI
- Ghosh, 2016, The transcription factor Pax6 contributes to the induction of GLT-1 expression in astrocytes through an interaction with a distal enhancer element, J. Neurochem., 136, 262, 10.1111/jnc.13406 · DOI
- Stacey, 2010, Drosophila Glial Glutamate Transporter Eaat1 Is Regulated by Fringe-Mediated Notch Signaling and Is Essential for Larval Locomotion, J. Neurosci., 30, 14446, 10.1523/JNEUROSCI.1021-10.2010 · DOI
- Lee, 2017, Brain endothelial cells induce astrocytic expression of the glutamate transporter GLT-1 by a Notch-dependent mechanism, J. Neurochem., 143, 489, 10.1111/jnc.14135 · DOI
- Robinson, 2020, Reciprocal communication between astrocytes and endothelial cells is required for astrocytic glutamate transporter 1 (GLT-1) expression, Neurochem. Int., 139, 104787, 10.1016/j.neuint.2020.104787 · DOI
- Hertz, 1978, GFA Content, Glutamate Uptake and Activity of Glutamate Metabolizing Enzymes in Differentiating Mouse Astrocytes in Primary Cultures, Dev. Neurosci., 1, 226, 10.1159/000112577 · DOI
- Goldman, 1984, Dibutyryl cyclic AMP causes intermediate filament accumulation and actin reorganization in astrocytes, Brain Res., 306, 85, 10.1016/0006-8993(84)90358-5 · DOI
- Pisano, 1996, Activation of the Adenylate Cyclase-dependent Protein Kinase Pathway Increases High Affinity Glutamate Uptake into Rat Striatal Synaptosomes, Neuropharmacology, 35, 541, 10.1016/0028-3908(96)84624-7 · DOI
- Perego, 2002, The GLT-1 and GLAST Glutamate Transporters Are Expressed on Morphologically Distinct Astrocytes and Regulated by Neuronal Activity in Primary Hippocampal Cocultures, J. Neurochem., 75, 1076, 10.1046/j.1471-4159.2000.0751076.x · DOI
- Simantov, 1999, Changes in expression of neuronal and glial glutamate transporters in rat hippocampus following kainate-induced seizure activity, Mol. Brain Res., 65, 112, 10.1016/S0169-328X(98)00349-0 · DOI
- Duan, 1999, Glutamate Induces Rapid Upregulation of Astrocyte Glutamate Transport and Cell-Surface Expression of GLAST, J. Neurosci., 19, 10193, 10.1523/JNEUROSCI.19-23-10193.1999 · DOI
- Zafra, 2016, Activity dependent internalization of the glutamate transporter GLT-1 mediated by β-arrestin 1 and ubiquitination, Neuropharmacology, 107, 376, 10.1016/j.neuropharm.2016.03.042 · DOI
- Piniella, 2019, Activity dependent internalization of the glutamate transporter GLT-1 requires calcium entry through the NCX sodium/calcium exchanger, Neurochem. Int., 123, 125, 10.1016/j.neuint.2018.03.012 · DOI
- Gamboa, 2002, Insulin-like growth factor-1 increases activity and surface levels of the GLAST subtype of glutamate transporter, Neurochem. Int., 40, 397, 10.1016/S0197-0186(01)00106-1 · DOI
- Boehmer, 2003, Regulation of the glutamate transporter EAAT1 by the ubiquitin ligase Nedd4-2 and the serum and glucocorticoid-inducible kinase isoforms SGK1/3 and protein kinase B, J. Neurochem., 86, 1181, 10.1046/j.1471-4159.2003.01937.x · DOI
- Stoykova, 1998, Pax6 Controls Radial Glia Differentiation in the Cerebral Cortex, Neuron, 21, 1031, 10.1016/S0896-6273(00)80621-2 · DOI
- Sakurai, 2008, The Neurogenesis-Controlling Factor, Pax6, Inhibits Proliferation and Promotes Maturation in Murine Astrocytes, J. Neurosci., 28, 4604, 10.1523/JNEUROSCI.5074-07.2008 · DOI
- Gegelashvili, 2000, The high-affinity glutamate transporters GLT1, GLAST, and EAAT4 are regulated via different signalling mechanisms, Neurochem. Int., 37, 163, 10.1016/S0197-0186(00)00019-X · DOI
- Namihira, 2009, Committed Neuronal Precursors Confer Astrocytic Potential on Residual Neural Precursor Cells, Dev. Cell, 16, 245, 10.1016/j.devcel.2008.12.014 · DOI
- Kopan, 2009, The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism, Cell, 137, 216, 10.1016/j.cell.2009.03.045 · DOI
- Fischer, 2007, Delta Notch and then? Protein interactions and proposed modes of repression by Hes and Hey bHLH factors, Nucleic Acids Res., 35, 4583, 10.1093/nar/gkm477 · DOI
- Aguirre, 2013, Involvement of the Notch Pathway in Terminal Astrocytic Differentiation: Role of PKA, ASN Neuro, 5, AN20130023, 10.1042/AN20130023 · DOI
- Biswas, 2018, Epigenetic tools (The Writers, The Readers and The Erasers) and their implications in cancer therapy, Eur. J. Pharmacol., 837, 8, 10.1016/j.ejphar.2018.08.021 · DOI
- Zhang, 2016, Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse, Neuron, 89, 37, 10.1016/j.neuron.2015.11.013 · DOI · Paper page
- Zhang, 2014, Regulation of DNA methylation by ethanol induces tissue plasminogen activator expression in astrocytes, J. Neurochem., 128, 344, 10.1111/jnc.12465 · DOI
- Broide, 2007, Distribution of histone deacetylases 1–11 in the rat brain, J. Mol. Neurosci., 31, 47, 10.1007/BF02686117 · DOI
- Zhang, 2016, Silencing of histone deacetylase 2 suppresses malignancy for proliferation, migration, and invasion of glioblastoma cells and enhances temozolomide sensitivity, Cancer Chemother. Pharmacol., 78, 1289, 10.1007/s00280-016-3188-2 · DOI
- Karki, 2014, Yin Yang 1 Is a Repressor of Glutamate Transporter EAAT2, and It Mediates Manganese-Induced Decrease of EAAT2 Expression in Astrocytes, Mol. Cell. Biol., 34, 1280, 10.1128/MCB.01176-13 · DOI
- Zschocke, 2007, DNA methylation dependent silencing of the human glutamate transporterEAAT2 gene in glial cells, Glia, 55, 663, 10.1002/glia.20497 · DOI
- Liu, 2005, The Excitatory Amino Acid Transporter-2 Induces Apoptosis and Decreases Glioma GrowthIn vitroandIn vivo, Cancer Res., 65, 1934, 10.1158/0008-5472.CAN-04-3626 · DOI
- Alam, 2019, Epigenetic Regulation of Excitatory Amino Acid Transporter 2 in Neurological Disorders, Front. Pharmacol., 10, 1510, 10.3389/fphar.2019.01510 · DOI
- Hardingham, 2007, Presynaptic Efficacy Directs Normalization of Synaptic Strength in Layer 2/3 Rat Neocortex After Paired Activity, J. Neurophysiol., 97, 2965, 10.1152/jn.01352.2006 · DOI
- Larkman, 1995, Synaptic plasticity: Hippocampal LTP, Curr. Opin. Neurobiol., 5, 324, 10.1016/0959-4388(95)80045-X · DOI
- Valtcheva, 2016, Astrocytes gate Hebbian synaptic plasticity in the striatum, Nat. Commun., 7, 13845, 10.1038/ncomms13845 · DOI
- Rajatileka, 2017, Variants of the EAAT2 Glutamate Transporter Gene Promoter Are Associated with Cerebral Palsy in Preterm Infants, Mol. Neurobiol., 55, 2013, 10.1007/s12035-017-0462-1 · DOI
- Poletti, 2014, Effect of glutamate transporter EAAT2 gene variants and gray matter deficits on working memory in schizophrenia, Eur. Psychiatry, 29, 219, 10.1016/j.eurpsy.2013.07.003 · DOI
- Parkin, 2020, Excitatory amino acid transporter (EAAT)1 and EAAT2 mRNA levels are altered in the prefrontal cortex of subjects with schizophrenia, J. Psychiatr. Res., 123, 151, 10.1016/j.jpsychires.2020.02.004 · DOI
- Bauer, 2008, Abnormal expression of glutamate transporter and transporter interacting molecules in prefrontal cortex in elderly patients with schizophrenia, Schizophr. Res., 104, 108, 10.1016/j.schres.2008.06.012 · DOI
- Jansen, 2016, Duplications of SLC1A3: Associated with ADHD and autism, Eur. J. Med Genet., 59, 373, 10.1016/j.ejmg.2016.06.003 · DOI
- Huang, 2019, A functional variant in SLC1A3 influences ADHD risk by disrupting a hsa-miR-3171 binding site: A two-stage association study, Genes Brain Behav., 18, e12574, 10.1111/gbb.12574 · DOI
- Blacker, 2019, EAAT2 as a Research Target in Bipolar Disorder and Unipolar Depression: A Systematic Review, Mol. Neuropsychiatry, 5, 1
- Bernard, 2011, Altered expression of glutamate signaling, growth factor, and glia genes in the locus coeruleus of patients with major depression, Mol. Psychiatry, 16, 634, 10.1038/mp.2010.44 · DOI · Paper page
- Choudary, 2005, Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression, Proc. Natl. Acad. Sci. USA, 102, 15653, 10.1073/pnas.0507901102 · DOI
- Soriano, 2007, Compartmentalized NMDA receptor signalling to survival and death, J. Physiol., 584, 381, 10.1113/jphysiol.2007.138875 · DOI
- Bell, 2011, The influence of synaptic activity on neuronal health, Curr. Opin. Neurobiol., 21, 299, 10.1016/j.conb.2011.01.002 · DOI · Paper page
- Parsons, 2014, Extrasynaptic NMDA Receptor Involvement in Central Nervous System Disorders, Neuron, 82, 279, 10.1016/j.neuron.2014.03.030 · DOI
- Soria, 2014, Extrasynaptic glutamate release through cystine/glutamate antiporter contributes to ischemic damage, J. Clin. Investig., 124, 3645, 10.1172/JCI71886 · DOI
- Frasca, 2011, Misplaced NMDA receptors in epileptogenesis contribute to excitotoxicity, Neurobiol. Dis., 43, 507, 10.1016/j.nbd.2011.04.024 · DOI
- Stark, 2011, Synaptic and Extrasynaptic NMDA Receptors Differentially Modulate Neuronal Cyclooxygenase-2 Function, Lipid Peroxidation, and Neuroprotection, J. Neurosci., 31, 13710, 10.1523/JNEUROSCI.3544-11.2011 · DOI
- Milnerwood, 2010, Early increase in extrasynaptic NMDA receptor signalling and expression contributes to phenotype onset in Huntington’s disease mice, Neuron, 65, 178, 10.1016/j.neuron.2010.01.008 · DOI
- Okamoto, 2009, Balance between synaptic versus extrasynaptic NMDA receptor activity influences inclusions and neurotoxicity of mutant huntingtin, Nat. Med., 15, 1407, 10.1038/nm.2056 · DOI
- Talantova, 2013, A induces astrocytic glutamate release, extrasynaptic NMDA receptor activation, and synaptic loss, Proc. Natl. Acad. Sci. USA, 110, E2518, 10.1073/pnas.1306832110 · DOI · Paper page
- Bordji, 2010, Activation of Extrasynaptic, But Not Synaptic, NMDA Receptors Modifies Amyloid Precursor Protein Expression Pattern and Increases Amyloid-β Production, J. Neurosci., 30, 15927, 10.1523/JNEUROSCI.3021-10.2010 · DOI
- Molokanova, 2014, Differential Effects of Synaptic and Extrasynaptic NMDA Receptors on Aβ-Induced Nitric Oxide Production in Cerebrocortical Neurons, J. Neurosci., 34, 5023, 10.1523/JNEUROSCI.2907-13.2014 · DOI
- Li, 2011, Soluble A Oligomers Inhibit Long-Term Potentiation through a Mechanism Involving Excessive Activation of Extrasynaptic NR2B-Containing NMDA Receptors, J. Neurosci., 31, 6627, 10.1523/JNEUROSCI.0203-11.2011 · DOI
- Xia, 2010, Memantine Preferentially Blocks Extrasynaptic over Synaptic NMDA Receptor Currents in Hippocampal Autapses, J. Neurosci., 30, 11246, 10.1523/JNEUROSCI.2488-10.2010 · DOI
- Lau, 2015, BDNF Reduces Toxic Extrasynaptic NMDA Receptor Signaling via Synaptic NMDA Receptors and Nuclear-Calcium-Induced Transcription of inhba/Activin A, Cell Rep., 12, 1353, 10.1016/j.celrep.2015.07.038 · DOI · Paper page
- Puddifoot, 2012, PGC-1 Negatively Regulates Extrasynaptic NMDAR Activity and Excitotoxicity, J. Neurosci., 32, 6995, 10.1523/JNEUROSCI.6407-11.2012 · DOI
- Karpova, 2013, Encoding and Transducing the Synaptic or Extrasynaptic Origin of NMDA Receptor Signals to the Nucleus, Cell, 152, 1119, 10.1016/j.cell.2013.02.002 · DOI
- Yan, 2020, Coupling of NMDA receptors and TRPM4 guides discovery of unconventional neuroprotectants, Science, 370, eaay3302, 10.1126/science.aay3302 · DOI
- Malik, A.R., and Willnow, T.E. (2019). Excitatory Amino Acid Transporters in Physiology and Disorders of the Central Nervous System. Int. J. Mol. Sci., 20. · DOI · Paper page
- Harris, 1996, Amyloid ? Peptide (25–35) Inhibits Na+?Dependent Glutamate Uptake in Rat Hippocampal Astrocyte Cultures, J. Neurochem., 67, 277, 10.1046/j.1471-4159.1996.67010277.x · DOI
- Beitz, 1997, The inhibitory effects of β-amyloid on glutamate and glucose uptakes by cultured astrocytes, Brain Res., 754, 65, 10.1016/S0006-8993(97)00043-7 · DOI
- Matos, 2008, Amyloid-beta peptide decreases glutamate uptake in cultured astrocytes: Involvement of oxidative stress and mitogen-activated protein kinase cascades, Neuroscience, 156, 898, 10.1016/j.neuroscience.2008.08.022 · DOI
- Robinson, 2000, Neuronal expression of glutamine synthetase in Alzheimer’s disease indicates a profound impairment of metabolic interactions with astrocytes, Neurochem. Int., 36, 471, 10.1016/S0197-0186(99)00150-3 · DOI
- Scott, 2002, Aberrant expression of the glutamate transporter excitatory amino acid transporter 1 (EAAT1) in Alzheimer’s disease, J. Neurosci., 22, 201, 10.1523/JNEUROSCI.22-03-j0004.2002 · DOI
- Hoshi, 2018, Altered expression of glutamate transporter-1 and water channel protein aquaporin-4 in human temporal cortex with Alzheimer’s disease, Neuropathol. Appl. Neurobiol., 44, 628, 10.1111/nan.12475 · DOI
- Rothstein, 1995, Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis, Ann. Neurol., 38, 73, 10.1002/ana.410380114 · DOI · Paper page
- Rothstein, 1992, Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis, N. Engl. J. Med., 326, 1464, 10.1056/NEJM199205283262204 · DOI
- Trotti, 2001, Amyotrophic Lateral Sclerosis-linked Glutamate Transporter Mutant Has Impaired Glutamate Clearance Capacity, J. Biol. Chem., 276, 576, 10.1074/jbc.M003779200 · DOI
- Gibb, 2007, A Caspase-3-cleaved Fragment of the Glial Glutamate Transporter EAAT2 Is Sumoylated and Targeted to Promyelocytic Leukemia Nuclear Bodies in Mutant SOD1-linked Amyotrophic Lateral Sclerosis, J. Biol. Chem., 282, 32480, 10.1074/jbc.M704314200 · DOI
- Gibb, 2006, Caspase-3 Cleaves and Inactivates the Glutamate Transporter EAAT, J. Biol. Chem., 281, 14076, 10.1074/jbc.M600653200 · DOI
- Deng, 1993, Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase, Science, 261, 1047, 10.1126/science.8351519 · DOI
- Sugiyama, 2018, Spinal cord-specific deletion of the glutamate transporter GLT1 causes motor neuron death in mice, Biochem. Biophys. Res. Commun., 497, 689, 10.1016/j.bbrc.2018.02.132 · DOI
- Proper, 2002, Distribution of glutamate transporters in the hippocampus of patients with pharmaco-resistant temporal lobe epilepsy, Brain, 125, 32, 10.1093/brain/awf001 · DOI
- Mathern, 1999, Hippocampal GABA and glutamate transporter immunoreactivity in patients with temporal lobe epilepsy, Neurology, 52, 453, 10.1212/WNL.52.3.453 · DOI
- Sarac, 2009, Excitatory amino acid transporters EAAT-1 and EAAT-2 in temporal lobe and hippocampus in intractable temporal lobe epilepsy, APMIS, 117, 291, 10.1111/j.1600-0463.2009.02443.x · DOI
- Domercq, 2006, Increased expression and function of glutamate transporters in multiple sclerosis, Neurobiol. Dis., 21, 154, 10.1016/j.nbd.2005.06.017 · DOI
- Sulkowski, 2008, Expression of glutamate transporters GLT-1 and GLAST in different regions of rat brain during the course of experimental autoimmune encephalomyelitis, Neurosci., 155, 45, 10.1016/j.neuroscience.2008.05.025 · DOI
- Vercellino, 2007, Altered Glutamate Reuptake in Relapsing-Remitting and Secondary Progressive Multiple Sclerosis Cortex: Correlation With Microglia Infiltration, Demyelination, and Neuronal and Synaptic Damage, J. Neuropathol. Exp. Neurol., 66, 732, 10.1097/nen.0b013e31812571b0 · DOI · Paper page
- Diniz, 2020, Astrocyte glutamate transporters are increased in an early sporadic model of synucleinopathy, Neurochem. Int., 138, 104758, 10.1016/j.neuint.2020.104758 · DOI
- Chung, 2008, Downregulation of glial glutamate transporters after dopamine denervation in the striatum of 6-hydroxydopamine-lesioned rats, J. Comp. Neurol., 511, 421, 10.1002/cne.21852 · DOI
- Albertini, 2015, Alterations in the motor cortical and striatal glutamatergic system and d-serine levels in the bilateral 6-hydroxydopamine rat model for Parkinson’s disease, Neurochem. Int., 88, 88, 10.1016/j.neuint.2015.07.005 · DOI
- Kim, 2016, DJ-1 deficiency impairs glutamate uptake into astrocytes via the regulation of flotillin-1 and caveolin-1 expression, Sci. Rep., 6, 28823, 10.1038/srep28823 · DOI
- Arzberger, 1997, Changes of NMDA Receptor Subunit (NR1, NR2B) and Glutamate Transporter (GLT1) mRNA Expression in Huntington’s Disease—An In Situ Hybridization Study, J. Neuropathol. Exp. Neurol., 56, 440, 10.1097/00005072-199704000-00013 · DOI
- Behrens, 2002, Impaired glutamate transport and glutamate-glutamine cycling: Downstream effects of the Huntington mutation, Brain, 125, 1908, 10.1093/brain/awf180 · DOI
- Scarr, 2018, Changed gene expression in subjects with schizophrenia and low cortical muscarinic M1 receptors predicts disrupted upstream pathways interacting with that receptor, Mol. Psychiatry, 23, 295, 10.1038/mp.2016.195 · DOI
- Melone, 2005, Clozapine reduces GLT-1 expression and glutamate uptake in astrocyte cultures, Glia, 50, 276, 10.1002/glia.20172 · DOI
- Medina, 2013, Glutamate transporters: A key piece in the glutamate puzzle of major depressive disorder, J. Psychiatr. Res., 47, 1150, 10.1016/j.jpsychires.2013.04.007 · DOI
- Purcell, 2001, Postmortem brain abnormalities of the glutamate neurotransmitter system in autism, Neurology, 57, 1618, 10.1212/WNL.57.9.1618 · DOI · Paper page
- Guo, 2019, Altered glial glutamate transporter expression in descending circuitry and the emergence of pain chronicity, Mol. Pain, 15, 1744806918825044, 10.1177/1744806918825044 · DOI
- Cirillo, 2011, Reactive astrocytosis-induced perturbation of synaptic homeostasis is restored by nerve growth factor, Neurobiol. Dis., 41, 630, 10.1016/j.nbd.2010.11.012 · DOI
- Cavaliere, 2007, Gliosis alters expression and uptake of spinal glial amino acid transporters in a mouse neuropathic pain model, Neuron Glia Biol., 3, 141, 10.1017/S1740925X07000695 · DOI
- Aguirre, 2008, Valproate-dependent transcriptional regulation of GLAST/EAAT1 expression: Involvement of Ying-Yang, Neurochem. Int., 52, 1322, 10.1016/j.neuint.2008.01.015 · DOI
- Ortega, A., and Schousboe, A. (2017). Glutamate Transport System as a Novel Therapeutic Target in Chronic Pain: Molecular Mechanisms and Pharmacology. Advances in Neurobiology, Springer. · DOI
- Chivukula, 2020, Functional consequences of SLC1A3 mutations associated with episodic ataxia 6, Hum. Mutat., 41, 1892, 10.1002/humu.24089 · DOI
- During, 1993, Extracellular hippocampal glutamate and spontaneous seizure in the conscious human brain, Lancet, 341, 1607, 10.1016/0140-6736(93)90754-5 · DOI
- Binder, 2006, Functional changes in astroglial cells in epilepsy, Glia, 54, 358, 10.1002/glia.20394 · DOI
- Selvaraj, 2018, C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca2+-permeable AMPA receptor-mediated excitotoxicity, Nat. Commun., 9, 1, 10.1038/s41467-017-02729-0 · DOI
- Allen, 2002, Abundant Tau Filaments and Nonapoptotic Neurodegeneration in Transgenic Mice Expressing Human P301S Tau Protein, J. Neurosci., 22, 9340, 10.1523/JNEUROSCI.22-21-09340.2002 · DOI
- Potier, 2010, Reduction in glutamate uptake is associated with extrasynaptic NMDA and metabotropic glutamate receptor activation at the hippocampal CA1 synapse of aged rats, Aging Cell, 9, 722, 10.1111/j.1474-9726.2010.00593.x · DOI
- Brothers, 2013, Riluzole Partially Rescues Age-Associated, but not LPS-Induced, Loss of Glutamate Transporters and Spatial Memory, J. Neuroimmune Pharmacol., 8, 1098, 10.1007/s11481-013-9476-2 · DOI
- Wolfe, 2019, Structure and Function of the γ-Secretase Complex, Biochemistry, 58, 2953, 10.1021/acs.biochem.9b00401 · DOI
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Metadata
- Authors
- Todd, A. C., & Hardingham, G. E.
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2020-12-17
- Volume
- 21
- Issue
- 24
- Pages
- 9607
- ISSN
- 1422-0067
- PMC
- PMC7766851
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- en
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