Development of Stable Cell Lines Expressing Different Subtypes of Gaba_A Receptors

References

• Barnard E., Seeburg P. Structural basis of the GABA-activated chloride channel: molecular biology and molecular electrophysiology. Adv. Biochem. Psychopharmacol. 1988; 45: 1–18
   PubMedGoogle Scholar
• Möhler H. GABAergic synaptic transmission. Regulation by drugs. Arzneim. Forsch./Drug Res. 1992; 42: 211–214
   PubMed Web of Science ®Google Scholar
• Squires R. F., Benson C., Braestrup C., Coupet J., Klepner C. A., Myers V. A., Beer B. Some properties of brain specific benzodiazepine receptors : new evidence for multiple receptors. Pharmacol. Biochem. Behav. 1979; 10: 825–830
   PubMed Web of Science ®Google Scholar
• Nayeem N., Green T. P., Martin I. L., Barnard E. A. Quaternary structure of the native GABAA receptor determined by electron microscopic image analysis. J. Neurochem. 1994; 62: 815–818
   PubMed Web of Science ®Google Scholar
• Wisden W., Laurie D. J., Monyer H., Seeburg P. H. The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. I. Telencephalon, Diencephalon and Mesencephalon. J. Neurosci. 1992; 12: 1040–1062
   PubMed Web of Science ®Google Scholar
• Araki T., Tohyama M. Region-specific expression of GABAA receptor α3 and α4 subunits mRNAs in the rat brain. Mol. Brain Res. 1992; 12: 293–314
   PubMedGoogle Scholar
• Persohn E., Malherbe P., Richards J. G. Comparative molecular neuroanatomy of cloned GABAA receptor subunits in the rat CNS. J. Comp. Neurol. 1992; 326: 193–216
   PubMed Web of Science ®Google Scholar
• Fritschy J. M., Benke D., Mertens S., Oertel W. H., Bachi T., Möhler H. Five subtypes of type A gamma-aminobutyric acid receptors identified in neurons by double and triple immunofluorescence staining with subunit-specific antibodies. Proc. Natl. Acad. Sci. 1992; 89: 6726–6730
   PubMed Web of Science ®Google Scholar
• Sigel E., Baur R., Trube G., Möhler H., Malherbe P. The effect of subunit composition of rat brain GABAA receptors on channel function. Neuron. 1990; 5: 703–711
   PubMed Web of Science ®Google Scholar
• Ebert B., Wafford K., Whiting P., Krogsgaard-Larsen P., Kemp J. Molecular pharmacology of γ-aminobutyric acid type A receptor agonists and partial agonists in oocytes injected with different α, β and γ receptor subunit combinations. Mol. Pharmacol. 1994; 46: 957–963
   PubMed Web of Science ®Google Scholar
• Pritchett D. B., Sontheimer H., Shivers B. D., Ymer S., Kettenmann H., Schofield P. R., Seeburg P. H. Importance of novel GABAA receptor subunit for benzodiazepine pharmacology. Nature 1989a; 338: 582–585
   PubMed Web of Science ®Google Scholar
• Pritchett D. B., Lüddens H., Seeburg P. H. Type I and type II GABAA-benzodiazepine receptors produced in transfected cells. Science 1989b; 245: 1389–1392
   PubMed Web of Science ®Google Scholar
• Lüddens H., Pritchett D. B., Köhler M., Killish I., Keinäen K., Monyer H., Sprengel R., Seeburg P. H. Cerebellar GABAA receptor selective for a behavioural alcohol antagonist. Nature 1990; 346: 648–651
   PubMed Web of Science ®Google Scholar
• Faure-Halley C., Graham D., Arbilla S., Langer S. Z. Expression and properties of recombinant α1β2γ2 and α1β2γ2 forms of the rat GABAA receptor. Eur. J. Pharmacol. Mol. Pharmacol. Section 1993; 246: 283–287
   PubMed Web of Science ®Google Scholar
• Carter C., Thomsen D., Im W., Lennon D., Ngo D., Gale W., Im H., Seeburg P., Smith M. Functional expression of GABAA chloride channels and benzodiazepine binding sites in baculovirus infected insect cells. Biotechnology 1992; 10: 679–681
   PubMedGoogle Scholar
• Gallager D. W., Yu J., Xu J., Ramabhadran T., Hartnett C., Brown M., Meyyappan M., Kostas C., Tallman J., Primus R. J. Chronic benzodiazepine effects on the GABAA receptor complex observed in vivo is replicated in an in vitro recombinant expression system. 25th Annual Meeting Society of Neuroscience. 1995; 1590, San Diego. poster n° 624.8
   Google Scholar
• Higuchi R. Recombinant PCR. PCR protocols with guide to methods and applications, M. A. Innis, D. H. Gelfand, J. J. Snisky, T. J. White. Academic Press, San Diego, California 1990; 117–183
   Google Scholar
• Melera P. W., Davide J. P., Hession C. A., Scotto K. W. Phenotypic expression in Escherichia coli and nucleotide sequence of two Chinese hamster lung cell cDNAs encoding different dihydrofolate reductases. Mol. Cell. Biol. 1984; 4: 38–48
   PubMed Web of Science ®Google Scholar
• Hussain A., Lewis S. D., Yu M., Melera P. W. Construction of a dominant selectable marker using a novel dihydrofolate reductase. Gene 1992; 112: 179–188
   PubMed Web of Science ®Google Scholar
• Chen C., Okayama H. High-efficiency transformation of mammalian cells by plasmid DNA. Mol. Cell. Biol. 1987; 7: 2745–2752
   PubMed Web of Science ®Google Scholar
• Graham D., Faure C., Besnard F., Langer S. Z. Pharmacological profile of benzodiazepine site ligands with recombinant GABAA receptor subtypes. Eur. Neuropsychopharm. 1996, in press
   PubMed Web of Science ®Google Scholar
• De Lean A., Munson P. J., Rodbard D. Simultaneous analysis of families of sigmoidal curves : application to bioassay, radioligand assay and physiological dose-response curves. Am. J. Physiol. 1978; 235: E97–E102
   PubMed Web of Science ®Google Scholar
• Hadingham K. L., Harkness P. C., McKernan R. M., Quirk K., Le Bourdellès B., Horne A. L., Kemp J. A., Barnard E. A., Ragan C. I., Whiting P. J. Stable expression of mammalian type A γ-aminobutyric acid receptors in mouse cells : demonstration of functional assembly of benzodiazepine-responsive sites. Proc. Natl. Acad. Sci. USA 1992; 89: 6378–6382
   PubMed Web of Science ®Google Scholar
• Wong G., Sei Y., Skolnick P. Stable expression of type 1 γ-aminobutyric acid A/benzodiazepine receptors in a transfected cell line. Mol. Pharmacol. 1992; 42: 996–1003
   PubMed Web of Science ®Google Scholar
• Hamilton B. J., Lennon D. L., Im H. K., Seeburg P. H., Carter D. B. Stable expression of cloned rat GABAA receptor subunits in a human kidney cell line. Neurosci. Letts 1993; 153: 206–209
   PubMed Web of Science ®Google Scholar
• Lingueglia E., Renard S., Waldmann R., Voilley N., Champigny G., Plass H., Lazdunski M., Barbry P. Different homologous subunits of the amiloride-sensitive Na+ channel are differently regulated by aldosterone. J. Biol. Chem. 1994; 269: 13736–13739
   PubMed Web of Science ®Google Scholar
• Green W. N., Claudio T. Acetylcholine receptor assembly : subunit folding and oligomerization occur sequentially. Cell 1993; 74: 57–69
   PubMed Web of Science ®Google Scholar
• Laurie D. J., Seeburg P. H., Wisden W. The distribution of 13 GABAA receptor subunit mRNAs in the rat brain. II. Olfactory bulb and cerebellum. J. Neurosc. 1992; 12: 1063–1076
   PubMed Web of Science ®Google Scholar
• Benke D., Fritschy J. M., Trzeciak A., Bannwarth W., Möhler H. Distribution, prevalence, and drug binding profile of γ-aminobutyric acid type A receptor subtypes differing in the β-subunit variant. J. Biol. Chem. 1994; 269: 27100–27107
   PubMed Web of Science ®Google Scholar
• Korpi E. R., Luddens H. Regional γ-aminobutyric acid sensitivity of t-butylbicyclophosphor [35S]thionate binding depends on γ-aminobutyric acidA receptor α subunit. Mol. Pharmacol. 1993; 44: 87–92
   PubMed Web of Science ®Google Scholar
• Lüddens H., Seeburg P. H., Korpi E. R. Impact of β and γ variants on ligand-binding properties of γ-aminobutyric acid type A receptors. Mol. Pharmacol. 1994; 45: 810–814
   PubMed Web of Science ®Google Scholar
• Hadingham K. L., Wingrove P. B., Wafford K. A., Bain C. J., Kemp J. A., Palmer K. J., Wilson A. W., Wilcox A. S., Sikela J. M., Ragan C. I., Whiting P. J. The role of the beta subunit in determining the pharmacology of human GABAA receptors. Mol. Pharmacol. 1993; 44: 1211–1218
   PubMed Web of Science ®Google Scholar
• Langer S. Z., Arbilla S. Limitations of benzodiazepine receptor nomenclature : a proposal for a pharmacological classification as omega receptor subtypes. Fundam. Clin. Pharmacol. 1988; 2: 159–170
   PubMed Web of Science ®Google Scholar
• Bénavidès J., Peny B., Ruano D., Vitorica J., Scatton B. Comparative autoradiographic distribution of central ω (benzodiazepine) modulatory site subtypes with high, intermediate and low affinity for zolpidem and alpidem. Brain Res. 1993; 604: 240–250
   PubMed Web of Science ®Google Scholar