Skip to main content
Log in

Potassium channel in rabbit corneal endothelium activated by external anions

  • Articles
  • Published:
The Journal of Membrane Biology Aims and scope Submit manuscript

Summary

The apical membrane of the rabbit corneal endothelium contains a potassium-selective ionic channel. In patch-clamp recordings, the probability of finding the channel in the open state (P o) depends on the presence of either HCO 3 or Cl in the bathing medium. In a methane sulfonate-containing bath,P o is <0.05 at all physiologically relevant transmembrane voltages. With 0mm [HCO 3 ] o at +60 mV,P o was 0.085 and increased to 0.40 when [HCO 3 ] o was 15mm. With 4mm [Cl] o at +60 mV,P o was 0.083 and with 150mm Cl,P o increased to 0.36. LowP o's are also found when propionate, sulphate, bromide, and nitrate are the primary bath anions. The mechanism of action of the anion-stimulated K+ channel gating is not yet known, but a direct action of pH seems unlikely. The alkalinization of cytoplasm associated with the addition of 10mm (NH4)2SO4 to the bath and the acidification accompanying its removal do not result in channel activation nor does the use of Nigericin to equilibrate intracellular pH with that of the bath over the pH range of 6.8 to 7.8. Channel gating also is not affected by bathing the internal surface of the patch with cAMP, cGMP, GTP-γ-s, Mg2+ or ATP. Blockers of Na/H+ exchange, Na+−HCO 3 cotransport, Na+−K+ ATPase and carbonic anhydrase do not block the HCO 3 stimulation ofP o. Several of the properties of the channel could explain some of the previously reported voltage changes that occur in corneal endothelial cells stimulated by extracellular anions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Anderson, E.I., Fischbarg, J., Spector, A. 1974. Disulfide stimulation of fluid transport and effect on ATP level in rabbit corneal endothelium.Exp. Eye Res. 19:1–10

    Google Scholar 

  • Boron, W.F., de Weer, P. 1976. Intracellular pH transients in squid giant axons caused by CO2, NH3 and metabolic inhibitors.J. Gen. Physiol. 67:91–112

    Google Scholar 

  • Colquhoun, D., Hawkes, A.G. 1983. The principles of the stochastic interpretation of ion-channel mechanisms.In: Single-Channel Recording. B. Sakmann and E. Neher, editors, pp. 135–175. Plenum: New York

    Google Scholar 

  • Cook, N.S. 1988. The pharmacology of potassium channels and their therapeutic potential.Trends Pharmacol. Sci. 9:21–28

    Google Scholar 

  • Dikstein, S. 1973. Efficiency and survival of the corneal endothelial pump.Exp. Eye Res. 15:639–644

    Google Scholar 

  • Dikstein, S., Maurice, D.M. 1972. The active control of corneal hydration.Israel J. Med. Sci. 8:1523–1528

    Google Scholar 

  • Fischbarg, J., Hernandez, J., Liebovitch, L.S., Koniarek, J.P. 1985. The mechanism of fluid and electrolyte transport across corneal endothelium: Critical revision and update of a model.Curr. Eye Res. 4:351–360

    Google Scholar 

  • Fischbarg, J., Lim, J.J., Bourguet, J. 1977. Adenosine stimulation of fluid transport across rabbit corneal endothelium.J. Membrane Biol. 35:95–112

    Google Scholar 

  • Hodson, S. 1971. Evidence for a bicarbonate-dependent sodium pump in corneal endothelium.Exp. Eye Res. 11:20–29

    Google Scholar 

  • Jentsch, T.J., Keller, S.K., Koch, M., Wiederholt, M. 1984a. Evidence for coupled transport of bicarbonate and sodium in cultured bovine corneal endothelial cells.J. Membrane Biol. 81:189–204

    Google Scholar 

  • Jentsch, T.J., Keller, S.K., Wiederholt, M. 1985a. Ion transport mechanisms in cultured bovine corneal endothelial cells.Curr. Eye Res. 4:361–369

    Google Scholar 

  • Jentsch, T.J., Koch, M., Bleckmann, H., Wiederholt, M. 1984b. Effect of bicarbonate, pH, methazolamide, and stilbenes on the intracellular potentials of cultured bovine corneal endothelial cells.J. Membrane Biol. 78:103–117

    Google Scholar 

  • Jentsch, T.J., Korbmacher, C., Janicke, I., Fischer, D.G., Stahl, F., Helbig, H., Hollwede, H., Cragoe, E.J., Jr., Keller, S.K., Weiderholt, M. 1988. Regulation of cytoplasmic pH of cultured bovine endothelial cells in the absence and presence of bicarbonate.J. Membrane Biol. 103:29–40

    Google Scholar 

  • Jentsch, T.J., Matthes, H., Keller, S.K., Wiederholt, M. 1985b. Anion dependence of electrical effects of bicarbonate and sodium on cultured bovine corneal endothelial cells.Pfluegers Arch. 403:175–185

    Google Scholar 

  • Jentsch, T.J., Stahlknecht, T.R., Hollwede, H., Fischer, D.G., Keller, S.K., Wiederholt, M. 1985c. A bicarbonate-dependent process inhibitable by disulfonic stilbenes and a Na+/H+ exchange mediate22Na++ uptake into cultured bovine corneal endothelium.J. Biol. Chem. 206:795–801

    Google Scholar 

  • Kaye, G., Tice, L. 1968. Studies on the cornea. V. Electron microscopic localization of adenosine triphosphatase activity in the rabbit cornea in relation to transport.Invest. Ophthalmol. 5:22–32

    Google Scholar 

  • Leuenberger, P., Novikoff, A. 1974. Localization of transport adenosine triphosphatase in rat cornea.J. Cell Biol. 60:721–731

    Google Scholar 

  • Liebovitch, L.S., Fischbarg, J. 1982/1983. Effects of inhibitors of passive Na+ and HCO 3 fluxes on electrical potential and fluid transport across rabbit corneal endothelium.Curr. Eye Res. 2:183–186

    Google Scholar 

  • Lim, J., 1982/1983. Effects of bicarbonate on the potential difference across the rabbit corneal endothelium.Curr. Eye Res. 2:529–535

    Google Scholar 

  • Lysio, A., Kvernes, S., Garlid, K., Ratkje, S.K. 1985. Ionic transport across corneal endothelium.Acta Ophthalmol. 63:116–125

    Google Scholar 

  • Midelfart, A., Ratkje, S.K. 1985. Amiloride inhibition of Na+-entry into corneal endothelium.Pfluegers Arch. 403:377–383

    Google Scholar 

  • Moczydlowski, E. 1986. Single-channel enzymology.In: Ion Channel Reconstitution. C. Miller, editor. pp. 75–113. Plenum, New York

    Google Scholar 

  • O'Grady, S.M., Palfrey, H.C., Field, M. 1987. Characteristics and functions of Na−K−Cl cotransport in epithelial tissues.Am. J. Physiol. 253:C177-C192

    Google Scholar 

  • Rae, J.L. 1985. The application of patch clamp methods to ocular epithelia.Curr. Eye Res. 4:409–420

    Google Scholar 

  • Rae, J.L. 1986. Single ionic channels in mammalian corneal endothelium.Invest. Ophthalmol. Vis. Sci. 27(Suppl):86

    Google Scholar 

  • Rae, J.L., Dewey, J.D., Cooper, K.E. 1988a. A Cs+ blockable, K+ selective ionic channel from rabbit corneal endothelium.Invest. Ophthalmol. Vis. Sci. 29(Suppl):175

    Google Scholar 

  • Rae, J.L., Dewey, J., Cooper, K. 1989. Properties of single potassium-selective ionic channels from the apical membrane of rabbit corneal endothelium.Exp. Eye Res. 49:591–609

    Google Scholar 

  • Rae, J.L., Levis, R.A., Eisenberg, R.S. 1988b. Ionic channels in ocular epithelia.In: Ion Channels. T. Narashi, editor. pp. 283–327. Plenum: New York

    Google Scholar 

  • Roos, A., Boron, W.F. 1981. Intracellular pH.Physiol. Rev. 61:296–434

    Google Scholar 

  • Sachs, F., Neil, J., Barkakati, N. 1982. The automated analysis of data from single ionic channels.Pfluegers Arch. 395:331–340

    Google Scholar 

  • Stoddard, J.S., Reuss, L. 1988. Dependence of cell membrane conductances on bathing solution HCO 3 /CO2 inNecturus gallbladder.J. Membrane Biol. 102:163–174

    Google Scholar 

  • Tervo, T., Palkama, A. 1975. Electron microscopic localization of adenosine triphosphatase (NaK-ATPase) activity in the rat cornea.Exp. Eye Res. 21:269–279

    Google Scholar 

  • Wiederholt, M., Jentsch, T.J., Keller, S.K. 1985. Electrogenic sodium-bicarbonate symport in cultured corneal endothelial cells.Pfluegers Arch. 405(Suppl. 1):S167-S171

    Google Scholar 

  • Wigham, C., Hodson, S. 1981. The effect of bicarbonate ion concentration on trans-endothelial short circuit in ox corneas.Curr. Eye Res. I:37–41

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rae, J.L., Dewey, J., Cooper, K. et al. Potassium channel in rabbit corneal endothelium activated by external anions. J. Membrain Biol. 114, 29–36 (1990). https://doi.org/10.1007/BF01869382

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01869382

Key Words

Navigation