Expression and Study of Ligand‐Gated Ion Channels in Xenopus laevis Oocytes

  • A. Kapur
  • J. M. C. Derry
  • R. S. Hansen
Reference work entry

Abstract:

The study of neurotransmitter ion channels has been greatly facilitated by use of the Xenopus laevis oocyte expression system. The reliable expression of exogenous receptors in the Xenopus oocyte, including those belonging to the ligand‐gated ion channel family, has provided a powerful means for investigating structure‐function relationships in these receptors using a variety of methods such as two‐electrode voltage clamp electrophysiology, patch‐clamp studies, and radioligand binding assays. The following chapter outlines morphology of Xenopus laevis frogs and oocytes, and reviews the advantages and limitations of using Xenopus oocytes to study exogenously expressed proteins. Techniques for oocyte isolation and preparation, in vitro preparation and injection of RNA transcripts, and subsequent functional analysis of expressed ligand‐gated ion channel receptors which include the nAChR, the GABAA receptor, the 5‐HT3 and glycine receptors, are discussed in detail. The use of the two‐electrode voltage clamp setup to characterize whole‐cell receptor currents, and the types of concentration‐effect experiments that can be performed using this arrangement, are reviewed. Additional uses of Xenopus oocytes in characterizing the structure‐activity relationship of these receptors are also explored.

List of Abbreviations:

RNA

ribonucleic acid

nAChR

nicotinic acetylcholine receptor

GABAA

γ‐aminobutyric type A

5‐HT3

5‐hydroxytryptamine type 3

References

  1. Akabas MH, Karlin A. 1995. Identification of acetylcholine receptor channel‐lining residues in the M1 segment of the alpha‐subunit. Biochemistry 34(39): 12496.CrossRefPubMedGoogle Scholar
  2. Barnard EA, Miledi R, Sumikawa K. 1982. Translational of exogenous messenger RNA coding for nicotinic acetylcholine receptors produces functional receptors in Xenopus oocytes. Proc R Soc Lond B 215: 241.CrossRefPubMedGoogle Scholar
  3. Boileau AJ, Baur R, Sharkey LM, Sigel E, Czajkowski C. 2002. The relative amount of cRNA coding for γ2 subunits affects stimulation by benzodiazepines in GABAA receptors expressed in Xenopus oocytes. Neuropharmacology 43: 695.CrossRefPubMedGoogle Scholar
  4. Brejc K, van Dijk WJ, Klaassen RV, Schuurmans M, van Der Oost J, et al. 2001. Crystal structure of an Ach‐binding protein reveals the ligand‐binding domain of nicotinic receptors. Nature 411: 269.CrossRefPubMedGoogle Scholar
  5. Chang Y, Weiss DS. 1999. Channel opening locks agonist onto the GABAC receptor. Nat Neurosci 2(3): 219.CrossRefPubMedGoogle Scholar
  6. Chang Y, Weiss DS. 2002. Site‐specific fluorescence reveals distinct structural changes with GABA receptor activation and antagonism. Nat Neurosci 5(11): 1163.CrossRefPubMedGoogle Scholar
  7. Chang Y, Covey DF, Weiss DS. 2000. Correlation of the apparent affinities and efficacies of γ–aminobutyric acidC receptor agonists. Mol Pharmacol 58(6): 1375.PubMedGoogle Scholar
  8. Colman A. 1984. Translation of eukaryotic messenger RNA in Xenopus oocytes. Transcription and translation: a practical approach. Rickwood D, Hames BD, editors. Washington, DC: Oxford University Press; pp. 271–302.Google Scholar
  9. Colquhoun D. 1998. Binding, gating, affinity and efficacy: the interpretation of structure–activity relationships for agonists and of the effects of mutating receptors. Br J Pharmacol 125(5): 924.CrossRefPubMedGoogle Scholar
  10. Dascal N. 1987. The use of Xenopus oocytes for the study of ion channels. CRC Crit Rev Biochem 22 (4): 317.CrossRefPubMedGoogle Scholar
  11. Dascal N, Landau EM, Lass Y. 1984. Xenopus oocyte resting potential, muscarinic responses and the role of calcium and cyclic GMP. J Physiol 352: 551.CrossRefPubMedCentralPubMedGoogle Scholar
  12. Davies PA, Pistis M, Hanna MC, Peters JA, Lambert JJ, et al. 1999. The 5‐HT3B subunit is a major determinant of serotonin‐receptor function. Nature 397 (6717): 359.CrossRefPubMedGoogle Scholar
  13. Dumont JN. 1972. Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals. J Morphol 136: 153.CrossRefPubMedGoogle Scholar
  14. Elsner HA, Honck HH, Willmann F, Kreienkamp HJ, Iglauer F. 2000. Poor quality of oocytes from Xenopus laevis used in laboratory experiments: prevention by use of antiseptic surgical technique and antibiotic supplementation. Comp Med 50(2): 206.PubMedGoogle Scholar
  15. Geib S, Sandoz G, Carlier E, Cornet V, Cheynet‐Sauvion V, De Waard M. 2001. A novel Xenopus oocyte expression system based on cytoplasmic coinjection of T7‐driven plasmids and purified T7‐RNA polymerase. Receptors Channels 7(5): 331.PubMedGoogle Scholar
  16. Goldin AL. 1992. Maintenance of Xenopus laevis and oocyte injection. Methods in Enzmology, Vol. 207. Ion Channels. Rudy B, Iverson LE, editors. London: Academic Press; pp. 266–279.CrossRefGoogle Scholar
  17. Grenningloh G, Rienitz A, Schmitt B, Methfessel C, Zensen M, et al. 1987. The strychnine‐binding subunit of the glycine receptor shows homology with nicotinic acetylcholine receptors. Nature 328: 215.CrossRefPubMedGoogle Scholar
  18. Gurdon JB, Lane CD, Woodland HR, Marbaix G. 1971. Use of frog eggs and oocytes for the study of messenger RNA and its translation in living cells. Nature. 233: 177.CrossRefPubMedGoogle Scholar
  19. Holden JH, Czajkowski C. 2002. Different residues in the GABA(A) receptor alpha 1T60–alpha K70 mediate GABA and SR‐95531 actions. J Biol Chem 277(21): 18785.CrossRefPubMedGoogle Scholar
  20. Joshi PR, Suryanarayanan A, Schulte MK. 2004. A vertical flow chamber for Xenopus oocyte electrophysiology and automated drug screening. J Neurosci Methods 132: 69.CrossRefPubMedGoogle Scholar
  21. Kusano K, Miledi R, Stinnakre J. 1982. Cholinergic and catecholaminergic receptors in the Xenopus oocyte membrane. J Physiol 328: 143.CrossRefPubMedCentralPubMedGoogle Scholar
  22. Le Caherec F, Bron P, Verbavatz JM, GarretA, Morel G, et al. 1996. Incorporation of proteins into (Xenopus) oocytes by proteoliposome microinjection: functional characterization of a novel aquaporin. J Cell Sci 109(Pt 6): 1285.PubMedGoogle Scholar
  23. Lupu‐ Meiri M, Shapira H, Oron Y. 1988. Hemispheric asymmetry of rapid chloride responses to inositol triphosphate and calcium in Xenopus oocytes. FEBS Lett 240(1,2): 83.CrossRefPubMedGoogle Scholar
  24. Maricq AV, Peterson AS, Brake AJ, Myers RM, Julius D. 1991. Primary structure and functional expression of the 5HT3 receptor, a serotonin‐gated ion channel. Science 254: 432.CrossRefPubMedGoogle Scholar
  25. Marshal J, Tigyi G, Miledi R. 1995. Incorporation of acetylcholine receptors and chloride channels in Xenopus oocytes injected with Torpedo electroplaque membranes. Proc Natl Acad Sci USA 92: 5224.CrossRefGoogle Scholar
  26. Miledi R. 1980. Intracellular calcium and the desensitization of acetylcholine receptors. Proc R Soc Lond B Biol Sci 209: 447.CrossRefPubMedGoogle Scholar
  27. Miledi R. 1982. A calcium‐dependent transient outward current in Xenopus laevis oocytes. Proc R Soc Lond B Biol Sci 215: 491.CrossRefPubMedGoogle Scholar
  28. Miledi R, Parker I. 1984. Chloride current induced by injection of calcium into Xenopus oocytes. J Physiol 357: 173.CrossRefPubMedCentralPubMedGoogle Scholar
  29. Mishina M, Tobimatsu T, Imoto K, Tanaka KI, Fujita Y, et al. 1985. Location of functional regions of acetylcholine receptor α‐subunit by site‐directed mutagenesis. Nature 313: 364.CrossRefPubMedGoogle Scholar
  30. Newell JG, Dunn SMJ. 2002. Functional consequences of the loss of high affinity agonist binding to gamma‐aminobutyric acid type A receptors. Implication for receptor desensitization. J Biol Chem 277(24): 21423.CrossRefPubMedGoogle Scholar
  31. Nishizaki T, Morales A, Gehle VM, Sumikawa K. 1994. Differential interactions of gentamicin with mouse junctional and extrajunctional ACh receptors expressed in Xenopus oocytes. Brain Res Mol Brain Res 21(1–2): 99.CrossRefPubMedGoogle Scholar
  32. Okamoto T, Sumikawa K. 1991. Antibiotics cause changes in the desensitization of ACh receptors expressed in Xenopus oocytes. Brain Res Mol Brain Res 9(1–2): 165.CrossRefPubMedGoogle Scholar
  33. Quick MW, Lester HA. 1994. Methods for expression of excitability proteins in Xenopus oocytes. Methods in Neuroscience. London: Academic Press, Vol. 19; pp. 261–279.Google Scholar
  34. Schenborn ET, Mierendorf RC. 1985. A novel transcription property of SP6 and T7 RNA polymerases: Dependence on template structure. Nucl Acids Res 13: 6223.CrossRefPubMedCentralPubMedGoogle Scholar
  35. Schnizler K, Kuster M, Methfessel C, Fejtl M. 2003. The roboocyte: Automated cDNA/mRNA injection and subsequent TEVC recording on Xenopus oocytes in 96‐well microtiter plates. Receptors Channels 9: 41.CrossRefPubMedGoogle Scholar
  36. Schofield PR, Darlison MG, Fujita N, Burt DR, Stephenson FA, et al. 1987. Sequence and functional expression of the GABAA receptor shows a ligand‐gated receptor superfamily. Nature 328: 221.CrossRefPubMedGoogle Scholar
  37. Sigel E, Buhr E. 1997. The benzodiazepine binding site of GABAA receptors. Trends Pharmacol Sci 18(11): 425.CrossRefPubMedGoogle Scholar
  38. Sigel E, Baur R, Kellenberger S, Malherbe P. 1992. Point mutations affecting antagonist affinity and agonist dependent gating of GABAA receptor channels. EMBO J 11(6): 2017.PubMedCentralPubMedGoogle Scholar
  39. Stühmer W, Parekh AB. 1995. Electrophysiological recordings from Xenopus oocytes. Single‐channel recording, Second edition. Sakmann B, Neher E, editors. New York: Plenum Press; pp 341–356.Google Scholar
  40. Sumikawa K, Houghton M, Emtage JS, Richards BM, Barnard EA. 1981. Active multi‐subunit ACh receptor assembled by translation of heterologous mRNA in Xenopus oocytes. Nature 292: 862.CrossRefPubMedGoogle Scholar
  41. Theodoulou FL, Miller AJ. 1995. Xenopus oocytes as a heterologous expression system. Methods Mol Biol 49: 317.PubMedGoogle Scholar
  42. Wagner DA, Czajkowski C. 2001. Structure and dynamics of the GABA binding pocket: a narrowing cleft that constricts during activation. J Neurosci 21(1): 67.PubMedGoogle Scholar
  43. Wallace RA, Steinhardt J. 1977. Maturation of Xenopus oocytes. II. Observations on membrane potential. Dev Biol 57: 305.CrossRefPubMedGoogle Scholar
  44. White MM, Aylwin M. 1990. Niflumic and flufenamic acids are potent reversible blockers of Ca2+‐activated Cl channels in Xenopus oocytes. Mol Pharmcol 37: 720.Google Scholar
  45. Woodward RM, Polenzani L, Miledi R. 1994. Effects of fenamates and other nonsteroidal anti‐inflammatory drugs on rat brain GABAA receptors expressed in Xenopus oocytes. J Pharmacol Exp Ther 268(2): 806.PubMedGoogle Scholar
  46. Xie Y, Cohen JB. 2001. Contributions of Torpedo nicotinic acetylcholine receptor γTrp‐55 and δTrp‐57 to agonist and competitive antagonist function. J Biol Chem 276(4): 2417.CrossRefPubMedGoogle Scholar
  47. Yang XC, Karschin A, Labarca C, Elroy‐Stein O, Moss B, et al. 1991. Expression of ion channels and receptors in Xenopus oocytes using vaccinia virus. FASEB J 5(8): 2209.PubMedGoogle Scholar
  48. Yao SYM, Cass CE, Young JD. 2000. The Xenopus oocyte expression system for the cDNA cloning and characterization of plasma membrane transport proteins. In: Membrane transport: A Practical Approach. Baldwin SA, editor. Oxford University Press, Oxford, pp. 47-78.Google Scholar

Copyright information

© Springer Science+Business Media, LLC 2007

Authors and Affiliations

  • A. Kapur
  • J. M. C. Derry
  • R. S. Hansen

There are no affiliations available

Personalised recommendations