Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1993 Jul;466:157–172.

Light-induced currents in Xenopus oocytes expressing bovine rhodopsin.

B E Knox 1, H G Khorana 1, E Nasi 1
PMCID: PMC1175472  PMID: 7692039

Abstract

1. We have investigated the functioning of bovine rod opsin, which is efficiently synthesized from RNA made by in vitro transcription, following injection into Xenopus oocytes. We found that oocytes expressing the gene for opsin exhibit light-dependent ionic currents only after pigment generation by incubation with 11-cis-retinal. These currents are similar to the endogenous muscarinic acetylcholine (ACh) response of oocytes, but their amplitude is substantially smaller. 2. In order to optimize the conditions for obtaining light-induced currents in RNA-injected oocytes, the native ACh response was examined under several conditions. It was found that elevated external calcium markedly enhances the muscarinic response and that these currents have a non-linear dependence on membrane voltage, increasing substantially with depolarization. 3. Using the optimal conditions for evoking the largest ACh responses, (28 mM [Ca2+]o, 0 mV, omission of serum and Hepes from the media), the light-evoked currents obtained in RNA-injected oocytes were remarkably enhanced, and responses to multiple light stimuli could be obtained. 4. The light response appeared to desensitize, even after long periods of recovery and pigment regeneration. By contrast, the ACh responses continued to appear normal. These results suggest that desensitization of photoresponses expressed in Xenopus oocytes involve changes at early stages of the pathway, resulting in a reduced ability of rhodopsin to couple to the endogenous signalling system.

Full text

PDF
157

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barish M. E. A transient calcium-dependent chloride current in the immature Xenopus oocyte. J Physiol. 1983 Sep;342:309–325. doi: 10.1113/jphysiol.1983.sp014852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benovic J. L., Mayor F., Jr, Somers R. L., Caron M. G., Lefkowitz R. J. Light-dependent phosphorylation of rhodopsin by beta-adrenergic receptor kinase. 1986 Jun 26-Jul 2Nature. 321(6073):869–872. doi: 10.1038/321869a0. [DOI] [PubMed] [Google Scholar]
  3. Berridge M. J. Inositol trisphosphate-induced membrane potential oscillations in Xenopus oocytes. J Physiol. 1988 Sep;403:589–599. doi: 10.1113/jphysiol.1988.sp017266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Boton R., Singer D., Dascal N. Inactivation of calcium-activated chloride conductance in Xenopus oocytes: roles of calcium and protein kinase C. Pflugers Arch. 1990 Apr;416(1-2):1–6. doi: 10.1007/BF00370214. [DOI] [PubMed] [Google Scholar]
  5. Dascal N., Ifune C., Hopkins R., Snutch T. P., Lübbert H., Davidson N., Simon M. I., Lester H. A. Involvement of a GTP-binding protein in mediation of serotonin and acetylcholine responses in Xenopus oocytes injected with rat brain messenger RNA. Brain Res. 1986 Dec;387(3):201–209. doi: 10.1016/0169-328x(86)90026-4. [DOI] [PubMed] [Google Scholar]
  6. Dascal N., Landau E. M., Lass Y. Xenopus oocyte resting potential, muscarinic responses and the role of calcium and guanosine 3',5'-cyclic monophosphate. J Physiol. 1984 Jul;352:551–574. doi: 10.1113/jphysiol.1984.sp015310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dascal N. The use of Xenopus oocytes for the study of ion channels. CRC Crit Rev Biochem. 1987;22(4):317–387. doi: 10.3109/10409238709086960. [DOI] [PubMed] [Google Scholar]
  8. Hanrahan J. W., Tabcharani J. A. Inhibition of an outwardly rectifying anion channel by HEPES and related buffers. J Membr Biol. 1990 Jun;116(1):65–77. doi: 10.1007/BF01871673. [DOI] [PubMed] [Google Scholar]
  9. Hargrave P. A., McDowell J. H. Rhodopsin and phototransduction: a model system for G protein-linked receptors. FASEB J. 1992 Mar;6(6):2323–2331. doi: 10.1096/fasebj.6.6.1544542. [DOI] [PubMed] [Google Scholar]
  10. Henselman R. A., Cusanovich M. A. Characterization of the recombination reaction of rhodopsin. Biochemistry. 1976 Nov 30;15(24):5321–5325. doi: 10.1021/bi00669a019. [DOI] [PubMed] [Google Scholar]
  11. Hirono C., Ito I., Sugiyama H. Neurotensin and acetylcholine evoke common responses in frog oocytes injected with rat brain messenger ribonucleic acid. J Physiol. 1987 Jan;382:523–535. doi: 10.1113/jphysiol.1987.sp016382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ito I., Hirono C., Yamagishi S., Nomura Y., Kaneko S., Sugiyama H. Roles of protein kinases in neurotransmitter responses in Xenopus oocytes injected with rat brain mRNA. J Cell Physiol. 1988 Jan;134(1):155–160. doi: 10.1002/jcp.1041340120. [DOI] [PubMed] [Google Scholar]
  13. Kato K., Kaneko S., Nomura Y. Phorbol ester inhibition of current responses and simultaneous protein phosphorylation in Xenopus oocyte injected with brain mRNA. J Neurochem. 1988 Mar;50(3):766–773. doi: 10.1111/j.1471-4159.1988.tb02980.x. [DOI] [PubMed] [Google Scholar]
  14. Kelleher D. J., Johnson G. L. Phosphorylation of rhodopsin by protein kinase C in vitro. J Biol Chem. 1986 Apr 5;261(10):4749–4757. [PubMed] [Google Scholar]
  15. Khorana H. G., Knox B. E., Nasi E., Swanson R., Thompson D. A. Expression of a bovine rhodopsin gene in Xenopus oocytes: demonstration of light-dependent ionic currents. Proc Natl Acad Sci U S A. 1988 Nov;85(21):7917–7921. doi: 10.1073/pnas.85.21.7917. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kusano K., Miledi R., Stinnakre J. Cholinergic and catecholaminergic receptors in the Xenopus oocyte membrane. J Physiol. 1982 Jul;328:143–170. doi: 10.1113/jphysiol.1982.sp014257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lupu-Meiri M., Shapira H., Matus-Leibovitch N., Oron Y. Two types of intrinsic muscarinic responses in Xenopus oocytes. I. Differences in latencies and 45Ca efflux kinetics. Pflugers Arch. 1990 Dec;417(4):391–397. doi: 10.1007/BF00370658. [DOI] [PubMed] [Google Scholar]
  18. Lupu-Meiri M., Shapira H., Oron Y. Extracellular calcium participates in responses to acetylcholine in Xenopus oocytes. FEBS Lett. 1990 Mar 26;262(2):165–169. doi: 10.1016/0014-5793(90)80180-q. [DOI] [PubMed] [Google Scholar]
  19. Matthews G., Neher E., Penner R. Second messenger-activated calcium influx in rat peritoneal mast cells. J Physiol. 1989 Nov;418:105–130. doi: 10.1113/jphysiol.1989.sp017830. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Miledi R. A calcium-dependent transient outward current in Xenopus laevis oocytes. Proc R Soc Lond B Biol Sci. 1982 Jul 22;215(1201):491–497. doi: 10.1098/rspb.1982.0056. [DOI] [PubMed] [Google Scholar]
  21. Miledi R., Parker I. Chloride current induced by injection of calcium into Xenopus oocytes. J Physiol. 1984 Dec;357:173–183. doi: 10.1113/jphysiol.1984.sp015495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Miledi R., Parker I. Latencies of membrane currents evoked in Xenopus oocytes by receptor activation, inositol trisphosphate and calcium. J Physiol. 1989 Aug;415:189–210. doi: 10.1113/jphysiol.1989.sp017718. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Miledi R., Parker I., Sumikawa K. Oscillatory chloride current evoked by temperature jumps during muscarinic and serotonergic activation in Xenopus oocyte. J Physiol. 1987 Feb;383:213–229. doi: 10.1113/jphysiol.1987.sp016405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Nomura Y., Kaneko S., Kato K., Yamagishi S., Sugiyama H. Inositol phosphate formation and chloride current responses induced by acetylcholine and serotonin through GTP-binding proteins in Xenopus oocyte after injection of rat brain messenger RNA. Brain Res. 1987 Jul;388(2):113–123. doi: 10.1016/s0006-8993(87)80004-5. [DOI] [PubMed] [Google Scholar]
  25. Oron Y., Dascal N., Nadler E., Lupu M. Inositol 1,4,5-trisphosphate mimics muscarinic response in Xenopus oocytes. Nature. 1985 Jan 10;313(5998):141–143. doi: 10.1038/313141a0. [DOI] [PubMed] [Google Scholar]
  26. Parker I., Miledi R. Changes in intracellular calcium and in membrane currents evoked by injection of inositol trisphosphate into Xenopus oocytes. Proc R Soc Lond B Biol Sci. 1986 Aug 22;228(1252):307–315. doi: 10.1098/rspb.1986.0057. [DOI] [PubMed] [Google Scholar]
  27. Parker I., Miledi R. Inositol trisphosphate activates a voltage-dependent calcium influx in Xenopus oocytes. Proc R Soc Lond B Biol Sci. 1987 Jun 22;231(1262):27–36. doi: 10.1098/rspb.1987.0033. [DOI] [PubMed] [Google Scholar]
  28. Parker I., Sumikawa K., Miledi R. Neurotensin and substance P receptors expressed in Xenopus oocytes by messenger RNA from rat brain. Proc R Soc Lond B Biol Sci. 1986 Nov 22;229(1255):151–159. doi: 10.1098/rspb.1986.0079. [DOI] [PubMed] [Google Scholar]
  29. Pepperberg D. R., Lurie M., Brown P. K., Dowling J. E. Visual adaptation: effects of externally applied retinal on the light-adapted, isolated skate retina. Science. 1976 Jan 30;191(4225):394–396. doi: 10.1126/science.1246621. [DOI] [PubMed] [Google Scholar]
  30. Shapira H., Wada E., Battey J. F., Jensen R. T., Coy D. H., Kusano K. Distinguishing bombesin receptor subtypes using the oocyte assay. Biochem Biophys Res Commun. 1991 Apr 15;176(1):79–86. doi: 10.1016/0006-291x(91)90892-b. [DOI] [PubMed] [Google Scholar]
  31. Shimada S., Spivak C., Uhl G. Endothelin receptor: a profoundly desensitizing receptor expressed in Xenopus oocytes. Eur J Pharmacol. 1991 Jan 25;193(1):123–125. doi: 10.1016/0014-2999(91)90211-8. [DOI] [PubMed] [Google Scholar]
  32. Singer D., Boton R., Moran O., Dascal N. Short- and long-term desensitization of serotonergic response in Xenopus oocytes injected with brain RNA: roles for inositol 1,4,5-trisphosphate and protein kinase C. Pflugers Arch. 1990 Apr;416(1-2):7–16. doi: 10.1007/BF00370215. [DOI] [PubMed] [Google Scholar]
  33. Snyder P. M., Krause K. H., Welsh M. J. Inositol trisphosphate isomers, but not inositol 1,3,4,5-tetrakisphosphate, induce calcium influx in Xenopus laevis oocytes. J Biol Chem. 1988 Aug 15;263(23):11048–11051. [PubMed] [Google Scholar]
  34. Tanaka K., Masu M., Nakanishi S. Structure and functional expression of the cloned rat neurotensin receptor. Neuron. 1990 Jun;4(6):847–854. doi: 10.1016/0896-6273(90)90137-5. [DOI] [PubMed] [Google Scholar]
  35. Tigyi G., Dyer D., Matute C., Miledi R. A serum factor that activates the phosphatidylinositol phosphate signaling system in Xenopus oocytes. Proc Natl Acad Sci U S A. 1990 Feb;87(4):1521–1525. doi: 10.1073/pnas.87.4.1521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Tsien R. W., Hess P., McCleskey E. W., Rosenberg R. L. Calcium channels: mechanisms of selectivity, permeation, and block. Annu Rev Biophys Biophys Chem. 1987;16:265–290. doi: 10.1146/annurev.bb.16.060187.001405. [DOI] [PubMed] [Google Scholar]
  37. Yamamoto D., Suzuki N. Blockage of chloride channels by HEPES buffer. Proc R Soc Lond B Biol Sci. 1987 Feb 23;230(1258):93–100. doi: 10.1098/rspb.1987.0011. [DOI] [PubMed] [Google Scholar]
  38. Yau K. W., Baylor D. A. Cyclic GMP-activated conductance of retinal photoreceptor cells. Annu Rev Neurosci. 1989;12:289–327. doi: 10.1146/annurev.ne.12.030189.001445. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES