GABA uptake and release by a mammalian cell line stably expressing a cloned rat brain GABA transporter

References

• Bernath S. Calcium-independent release of amino acid neurotransmitters: fact or artifact?. Progress in Neurobiology 1992; 38: 57–91
   Google Scholar
• Borden L. A., Smith K. E., Hartig P. R., Branchek T. A., Weinshank R. L. Molecular heterogeneity of the γ-aminobutyric acid (GABA) transport system. Journal of Biological Chemistry 1992; 267: 21098–21104
   PubMed Web of Science ®Google Scholar
• Bowery N. G., Jones G. P., Neal M. J. Selective ínhibition of neuronal GABA uptake by cis-1,3-aminocyclohexane carboxylic acid. Nature 1976; 264: 281–284
   Google Scholar
• Cabantchik Z. I., Greger R. Chemical probes for anion transporters of mammalian cell membranes. American Journal of Physiology 1992; 262: C803–C827
   Google Scholar
• Carvalho C. M., Bandeira-Duarte C., Ferreira I. L., Carvalho A. P. Regulation of carrier-mediated and exocytotic release of [3H]GABA in rat brain synaptosomes. Neurochemical Research 1991; 16: 763–772
   Google Scholar
• Clark J. A., Deutch A. Y., Gallipoli P. Z., Amara S. G. Functional expression and CNS distribution of a β-alanine sensitive neuronal GABA transporter. Neuron 1992; 9: 337–348
   Google Scholar
• Erecinska M., Troeger M. B. Amino acid neurotransmitters in the CNS. Characteristics of the acidic amino acid exchange. FEBS Letters 1986; 199: 95–99
   Google Scholar
• Giros B., Mestikawy S., Bertrand L., Caron M. G. Cloning and functional characterization of a cocaine-sensitive dopamine transporter. FEBS Letters 1991; 295: 149–154
   PubMed Web of Science ®Google Scholar
• Guastella J., Nelson N., Nelson H., Czyzyk L., Keynan S., Miedel M. C., Davidson N., Lester H. A., Kanner B. I. Cloning and expression of a rat brain GABA transporter. Science 1990; 249: 1303–1306
   PubMed Web of Science ®Google Scholar
• Guastella J., Brecha N., Weigmann C., Lester H. A., Davidson N. Cloning, expression, and localization of a rat brain high-affinity glycine transporter. Proceedings of the National Academy of Sciences, USA 1992; 89: 7189–7193
   PubMed Web of Science ®Google Scholar
• Henn F. A., Hamberger A. Glial cell function: uptake of transmitter substances. Proceedings of the National Academy of Sciences, USA 1971; 68: 2686–2690
   PubMed Web of Science ®Google Scholar
• Hoffman B. J., Mezey E., Brownstein M. J. Cloning of a serotonin transporter affected by antidepressants. Science 1991; 254: 579–580
   PubMed Web of Science ®Google Scholar
• Hutchison H. T., Werrbach K., Vance C., Haber B. Uptake of neurotransmitters by clonal lines of astrocytoma and neuroblastoma in culture. I. Transport of γ-aminobutyric acid. Brain Research 1974; 66: 265–274
   Google Scholar
• Kammermans M., Werblin F. GABA-mediated positive autofeedback loop controls horizontal cell kinetics in tiger salamander retina. Journal of Neuroscience 1992; 12: 2451–2463
   Google Scholar
• Kanner B. I. Active transport of γ-aminobutyric acid by membrane vesicles isolated from rat brain. Biochemistry 1978; 17: 1207–1211
   PubMed Web of Science ®Google Scholar
• Karbon E. W., Enna S. J., Ferkany J. W. Biochemical and behavioral studies following subchronic administration of GABA uptake inhibitors in mice. Neuropharmacology 1991; 30: 1187–1192
   Google Scholar
• Keynan S., Suh Y.-J., Kanner B. I., Rudnick G. Expression of a cloned γ-aminobutyric acid transporter in mammalian cells. Biochemistry 1992; 31: 1974–1979
   Google Scholar
• Kilty J. E., Lorang D., Amara S. G. Cloning and expression of a cocaine-sensitive rat dopamine transporter. Science 1991; 254: 578–579
   PubMed Web of Science ®Google Scholar
• Krogsgaard-Larsen P. Inhibitors of the GABA uptake systems. Molecular and Cellular Biochemistry 1980; 31: 105–121
   PubMed Web of Science ®Google Scholar
• Larsson O. M., Falch E., Krogsgaard-Larsen P., Schousboe A. Kinetic characterization of inhibition of γ-aminobutyric acid uptake into cultured neurons and astrocytes by 4,4-diphenyl-3-butenyl derivatives of nipecotic acid and guvacine. Journal of Neurochemistry 1988; 50: 818–823
   Google Scholar
• Levi G., Raiteri M. Exchange of neurotransmitter amino acid at nerve endings can simulate high affinity uptake. Nature 1974; 250: 735–737
   Google Scholar
• Lewin L., Mattsson M.-O., Rassin D. K., Sellstrom A. On the activity of γ-aminobutyric acid and glutamate transporters in chick embryonic neurons and rat synaptosomes. Neurochemical Research 1992; 17: 333–337
   Google Scholar
• Mager S., Naeve J., Quick M., Labarca C., Davidson N., Lester H. A. Steady states, charge movements, and rates for a cloned GABA transporter expressed in Xenopus oocytes. Neuron 1993; 1993: 177–188
   Google Scholar
• Malchow R. P., Ripps H. Effects of γ-aminobutyric acid on skate retinal horizontal cells: evidence for an electrogenic uptake mechanism. Proceedings of the National Academy of Sciences, USA 1990; 87: 8945–8949
   Google Scholar
• Martin D. L. Carrier-mediated transport and removal of GABA from synaptic regions. GABA in Nervous System Function, E. Roberts, T. N. Chase, D. B. Tower. Raven Press, New York 1976; 347–387
   Google Scholar
• Meldrum B. S. Epilepsy and γ-aminobutyric acid-mediated inhibition. International Review of Neurobiology 1976; 17: 1–36
   Google Scholar
• Neal M. J., Iversen L. L. Subcellular distribution of endogenous and [3H]γ-aminobutyric acid in rat cerebral cortex. Journal of Neurochemistry 1969; 16: 1245–1252
   Google Scholar
• Nelson M. T., Blaustein M. P. GABA efflux from synaptosomes: effects of membrane potential and external GABA and cations. Journal of Membrane Biology 1982; 69: 213–223
   PubMed Web of Science ®Google Scholar
• Nicholls D. G. Release of glutamate, aspartate, and γ-aminobutyric acid from isolated nerve terminals. Journal of Neurochemistry 1989; 52: 331–341
   PubMed Web of Science ®Google Scholar
• Pacholczyk T., Blakely R. D., Amara S. G. Expression cloning of a cocaine- and antidepressant-sensitive human noradrenaline transporter. Nature 1991; 350: 350–354
   PubMed Web of Science ®Google Scholar
• Passow H., Wood P. G., Lepke S., Muller H., Sovak M. Exploration of the functional significance of the stilbene disulfonate binding site in mouse band 3 by site-directed mutagenesis. Biophysics Journal 1992; 62: 98–100
   Google Scholar
• Radian R., Kanner B. I. Stoichiometry of sodium- and chloride-coupled γ-aminobutyric acid transport by synaptic plasma membrane vesicles isolated from rat brain. Biochemistry 1983; 22: 142–168
   Google Scholar
• Raiteri M., Federico R., Coletti A., Levi G. Release and exchange studies relating to the synaptosomal uptake of GABA. Journal of Neurochemistry 1975; 24: 1243–1250
   Google Scholar
• Sambrook J., Fritsch E. F., Maniatis T. Molecular cloning: A Laboratory Manual. Cold Spring Harbor Press, New York 1989
   Google Scholar
• Schon F. E., Kelly J. S. Autoradiographic localization of [3H]GABA and [3H]glutamate over satellite glial cells. Brain Research 1974a; 66: 275–288
   Google Scholar
• Schon F. E., Kelly J. S. The characterization of [3H]GABA uptake into the satellite glial cells of rat sensory ganglia. Brain Research 1974b; 66: 289–300
   Google Scholar
• Schon F. E., Kelly J. S. Selective uptake of [3H]β-alanine by glia-association with glial uptake system for GABA. Brain Research 1975; 86: 243–257
   PubMed Web of Science ®Google Scholar
• Schousboe A., Thorbek P., Hertz L., Krogsgaard-Larsen P. Effects of GABA analogues of restricted conformation of GABA transport in astrocytes and brain cortex slices and on GABA receptor binding. Journal of Neurochemistry 1979; 33: 181–189
   Google Scholar
• Schousboe A., Larsson O. M., Wood J. D., Krogsgaard-Larsen P. Transport and metabolism of γ-aminobutyric acid in neurons and glia: implications for epilepsy. Epilepsia 1983; 24: 531–538
   Google Scholar
• Schousboe A., Hjeds H., Engler J., Krogsgaard-Larsen P., Wood J. D. Tissue distribution, metabolism, anticonvulsant efficacy and effect on brain amino acid levels of the glia-selective γ-aminobutyric acid transport inhibitor 4,5,6,7-tetrahydroisoxazolo[4,5-c]pyrindin-3-ol in mice and chicks. Journal of Neurochemistry 1986; 47: 758–763
   Google Scholar
• Schwartz E. A. Depolarization without calcium can release gamma-aminobutyric acid from retinal neuron. Science 1987; 238: 350–355
   PubMed Web of Science ®Google Scholar
• Sellstrom A., Hamberger A. Neuronal and glial systems for γ-aminobutyric acid transport. Journal of Neurochemistry 1975; 24: 847–852
   Google Scholar
• Shimada S., Kitayama S., Lin C.-L., Patel A., Nanthakumar E., Gregor P., Kuhar M., Uhl G. Cloning and expression of a cocaine-sensitive dopamine transporter complementary DNA. Science 1991; 254: 576–578
   PubMed Web of Science ®Google Scholar
• Smith K. E., Borden L. A., Hartig P. R., Branchek T., Weinshank R. L. Cloning and expression of a glycine transporter reveal colocalization with NMDA receptors. Neuron 1992a; 8: 927–935
   PubMed Web of Science ®Google Scholar
• Smith K. E., Borden L. A., Wang C.-H., Hartig P. R., Branchek T. A., Weinshank R. L. Cloning and expression of a high affinity taurine transporter from rat brain. Molecular Pharmacology 1992b; 42: 563–569
   PubMed Web of Science ®Google Scholar
• Swinyard E. A., White H. S., Wolf H. H., Bondinell W. E. Anticonvulsant profiles of the potent and orally active GABA uptake inhibitors SK&F 89976-A and SK&F 100330-A and four prototype antiepileptic drugs in mice and rats. Epilepsia 1991; 32: 569–577
   Google Scholar
• Uchida S., Kwon J. M., Yamauchi A., Preston A. S., Marumo F., Handler J. S. Molecular cloning of the cDNA for an MDCK cell Na+- and Cl--dependent taurine transporter that is regulated by hypertonicity. Proceedings of the National Academy of Sciences, USA 1992; 89: 8230–8234
   PubMed Web of Science ®Google Scholar
• Usdin T. B., Mezey E., Chen C., Brownstein M. J., Hoffman B. J. Cloning of the cocaine-sensitive bovine dopamine transporter. Proceedings of the National Academy of Sciences, USA 1991; 88: 11168–11171
   Google Scholar
• Waldemeir P. C., Wicki P., Feldtrauer J. J., Baumann P. A. The measurement of release of endogenous GABA from rat brain slices by liquid chromatography with electrochemical detection. Naunyn-Schmiedeberg's Archives of Pharmacology 1988; 337: 284–288
   Google Scholar
• Yamauchi A., Uchida S., Kwon H. M., Preston A. S., Robey R. B., Garcia-Perez A., Burg M. B., Handler J. S. Cloning of a Na+- and Cl--dependent betaine transporter that is regulated by hypertonicity. Journal of Biological Chemistry 1992; 267: 649–652
   PubMedGoogle Scholar
• Yunger L. M., Fowler P. J., Zarevics P., Setler P. Novel inhibitors of γ-aminobutyric acid (GABA) uptake: anticonvulsant actions in rats and mice. Journal of Pharmacology and Experimental Therapeutics 1984; 228: 109–115
   PubMed Web of Science ®Google Scholar