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Characterization of a voltage-dependent Ca2+-selective channel from wheat roots

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Abstract

A new mechanism for calcium flux in wheat (Triticum aestivum L.) root cells has been characterized. Membrane vesicles were enriched in plasma membrane using aqueous-polymer two-phase partitioning and incorporated into artificial lipid bilayers, allowing characterization of single channels under voltage-clamp conditions. Membrane marker activities showed 74% and 83% purity in plasma membrane when expressed in terms of membrane area and activity, respectively. Since membrane vesicles obtained by aqueous-polymer two-phase partitioning yield a population of membrane vesicles of regular orientation, and vesicle fusion into planar lipid bilayers occurs in a defined manner, the orientation of the channel upon vesicle incorporation could be determined. Thus ionic activities and potentials could be controlled appropriately on what we propose to be the cytosolic (trans) and extracellular (cis) faces of the channel. The unitary conductance in symmetrical 1 mM CaCl2 was 27±0.4 (pS). The correlation between the theoretical and observed reversal potentials in asymmetrical conditions showed that the channel was highly selective for Ca2+ over Cl. Experiments simulating physiological ionic conditions showed a PCa 2+/PK + of 17–26, decreasing in this range as the extracellular CaCl2 concentration increased from 0.1 to 1 mM. The channel was also permeable to the essential nutrient ions, Mg2+ and Mn2+. The open probability of the channel was strongly dependent on the membrane potential. Inactivation with time was observed at more negative membrane potentials, and was immediately reversed as soon as the membrane potential was decreased. At membrane potentials more negative than -130mV, the channel remained mainly in the closed state, suggesting that in vivo the channel would remain largely closed and would open only upon membrane depolarization. The channel was blocked by micromolar concentrations of extracellular verapamil and trivalent cations, Al3+ being the most effective of those tested. Exposure of the cytosolic and extracellular sides of the channel to inositol 1,4,5-trisphosphate had no effect on the channel activity. We suggest a plasma-membrane origin for the channel as shown by biochemical and electrophysiological evidence, and discuss possible physiological roles of this channel, both in Ca2+ uptake into roots and in signal transduction.

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Abbreviations

IP3 :

1,4,5-trisphosphate

PM:

plasma membrane

References

  • Alexandre, J., Lassalles, J.P. (1992) Intracellular Ca2+ release by InsP3 in plants and effect of buffers on Ca2+ diffusion. Philos. Trans. R. Soc. London Ser. B 338, 53–61

    Google Scholar 

  • Alexandre, J., Lassalles, J.P., Kado, R.T. (1990) Opening of Ca2+ channels in isolated red beet root vacuole membrane by inositol 1,4,5-trisphosphate. Nature 343, 567–570

    Google Scholar 

  • Alexandrov, A.A., Alexandrova, L.A., Berestovsky, G.N. (1990) Block of Ca2+ channel from algae cells reconstituted in planar lipid bilayers by verapamil. Stud. Biophys. 138, 127–130

    Google Scholar 

  • Allen, G., Sanders, D. (1994) Two voltage-gated, calcium release channels coreside in the vacuolar membrane of broad bean guard cells. Plant Cell 6, 685–694

    Google Scholar 

  • Brosnan J.M., Sanders D. (1990) Inositol trisphosphate-mediated Ca2+ release in beet microsomes is inhibited by heparin. FEBS Lett. 260, 70–72

    Google Scholar 

  • Cohen, S. (1986) Fusion of liposomes to planar bilayers. In: Ion channel reconstitution, pp. 131–139. Miller, C., ed. Plenum Press, New York

    Google Scholar 

  • Colquhoun, D., Sigworth, F.J. (1983) Fitting and statistical analysis of single channel records. In: Single-channel recording, pp. 191–264. Sakman, B., Neher, E., eds. Plenum Press, N.Y. London

    Google Scholar 

  • Cosgrove, D.J., Hedrich, R. (1991) Stretch-activated chloride, potassium, and calcium channels coexisting in plasma membranes of guard cells of Vicia faba L. Planta 186, 143–153

    Google Scholar 

  • Ding, J.P., Pickard, B.G. (1993) Mechanosensory calcium-selective cation channels in epidermal cells. Plant J. 3, 83–110

    Google Scholar 

  • Evans, D.E., Briars, S.A., Williams, L. (1991) Active calcium transport by plant cell membranes. J. Exp. Bot. 42, 285–303

    Google Scholar 

  • Fatt, P., Ginsborg, B.L. (1958) The ionic requirements for the production of action potentials in crustacean muscle fibres. J. Physiol. 142, 516–543

    Google Scholar 

  • Gelli, A., Blumwald, E. (1993) Calcium retrieval from vacuolar pools. Characterization of a vacuolar calcium channel. Plant Physiol. 102, 1139–1146

    Google Scholar 

  • Graziana, A., Fosset, M., Ranjeva, R., Hetherington, A.M., Lazdunski, M. (1988) Ca2+ channel inhibitors that bind to plant cell membranes block Ca2+ entry into protoplasts. Biochemistry 27, 764–768

    Google Scholar 

  • Hanke, W. (1986) Incorporation of ion channels by fusion. In: Ion channel reconstitution, pp. 141–153. Miller, C., ed. Plenum Press, New York

    Google Scholar 

  • Harvey, H., Venis, M., Trewavas, J. (1989) Partial purification of a protein from maize (Zea mays) coleoptile membranes binding the Ca2+-channel antagonist verapamil. Biochem. J. 257, 95–100

    Google Scholar 

  • Hille, B. (1992) Ionic channels of excitable membranes, 2nd edn. Sinauer Associates Inc., Sunderland, Massachusetts

    Google Scholar 

  • Hodick, D., Sievers, A. (1988) The action potential of Dionaea muscipula Ellis. Planta 174, 8–18

    Google Scholar 

  • Huang, J.W., Grunes, D.L., Kochian, L. (1992a) Aluminium effects on the kinetics of calcium uptake into cells of the wheat root apex. Quantification of calcium fluxes using a calcium-selective vibrating microelectrode. Planta 188, 414–421

    Google Scholar 

  • Huang, J.W., Shaff, J.E., Grunes, D.L., Kochian, L.V. (1992b) Aluminium effects on calcium fluxes at the root apex of aluminium-tolerant and aluminium-sensitive wheat cultivars. Plant Physiol. 98, 230–237

    Google Scholar 

  • Johannes, E., Brosnan, J.M., Sanders, D. (1991) Calcium channels and signal transduction in plant cells. BioEssays 13, 331–336

    Google Scholar 

  • Johannes, E., Brosnan, J.M., Sanders, D. (1992a) Calcium channels in the vacuolar membrane of plants: multiple pathways for intracellular calcium mobilization. Philos. Trans. R. Soc. London Ser. B 338, 105–112

    Google Scholar 

  • Johannes, E., Brosnan, J.M., Sanders, D. (1992b) Parallel pathways for intracellular Ca2+ release from the vacuole of higher plants. Plant J. 2, 97–102

    Google Scholar 

  • Klughammer, B., Benz, R., Betz, M., Thume, M., Dietz, K. (1992a) Reconstitution of vacuolar ion channels into planar lipid bilayers. Biochim. Biophys. Acta 1104, 308–316

    Google Scholar 

  • Klughammer, B., Betz, M., Benz, R., Dietz, K.J. (1992b) Partial purification of a potassium channel with low permeability for sodium from tonoplast membranes of Hordeum vulgare cv. Gerbel. J. Membr. Biol. 128, 17–25

    Google Scholar 

  • Larsson, C., Widell, S., Kjellbom, P. (1987) Preparation of high-purity plasma membranes. Methods Enzymol. 148, 558–568

    Google Scholar 

  • Maathius F.J., Sanders, D. (1993) Energization of potassium uptake in Arabidopsis thaliana. Planta 191, 302–307

    Google Scholar 

  • Morré, D.J., Buckhout, T.J. (1979). In: Plant organelles, pp. 117–134. Reid, E., ed. Ellis Horwood, Chichester

  • Pantoja, O., Gelli, A., Blumwald, E. (1992) Voltage-dependent calcium channels in plant vacuoles. Science 255, 1567–1570

    Google Scholar 

  • Ping, Z., Yabe, I., Muto, S. (1992) Voltage-dependent Ca2+ channels in the plasma membrane and the vacuolar membrane of Arabidopsis thaliana. Biochim. Biophys. Acta 1112, 278–290

    Google Scholar 

  • Pineros, M., Tester, M. (1993) Plasma membrane Ca2+ channels in roots of higher plants and their role in aluminium toxicity. Plant Soil 155/156, 119–122

    Google Scholar 

  • Reid, R.J., Tester, M. (1992) Measurements of Ca2+ fluxes in intact plant cells. Philos. Trans. R. Soc. London Ser. B 338, 73–82

    Google Scholar 

  • Reid, R.J., Tester, M., Smith, F.A. (1994) Calcium/Aluminium interactions in the cell wall and plasma membrane of Chara. Planta, in press

  • Rengel, Z., Elliot, D. (1992a) Mechanisms of aluminium inhibition of net 45Ca2+ uptake by Amaranthus protoplasts. Plant Physiol. 98, 632–638

    Google Scholar 

  • Rengel, Z., Elliot, D. (1992b) Aluminium inhibits net 45Ca2+ uptake by Amaranthus protoplasts. Biochem. Physiol. Pflanz. 188, 177–186

    Google Scholar 

  • Rengel, Z., Pineros, M., Tester, M. (1994) Transmembrane calcium fluxes during Al stress. In: Proceedings of the third international symposium on plant-soil interactions at low pH. Brisbane, September 1993, Kluwer Academic, in press

  • Rosenberg, R., Hess, P., Tsien, R. (1988) Cardiac calcium channels in planar lipid bilayers. L-type channels and calcium-permeable channels open at negative membrane potentials. J. Gen. Physiol. 92, 27–54

    Google Scholar 

  • Ryan, P.R., Kochian, L.V. (1993) Interaction between aluminium toxicity and calcium uptake at the root apex in near-isogenic lines of wheat (Triticum aestivum L.) differing in aluminium tolerance. Plant Physiol. 102, 975–982

    Google Scholar 

  • Schroeder, J.I., Hagiwara, S. (1990) Repetitive increseases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels. Proc. Natl. Acad. Sci. USA 87, 9305–9309

    Google Scholar 

  • Schumaker, K.S., Sze, H. (1987) Inositol 1,4,5-trisphosphate release Ca2+ from vacuolar membrane vesicles of oat roots. J. Biol. Chem. 262, 3944–3946

    Google Scholar 

  • Shiina, T, Tazawa, M. (1986) Regulation of membrane excitation by protein phosphorylation in Nitellopsis obtusa. Protoplasma 134, 60–61

    Google Scholar 

  • Tester, M. (1990) Plant ion channels: whole-cell and single-channel studies. New Phytol. 114, 305–340

    Google Scholar 

  • Tester, M., Harvey, H. (1989) Verapamil-binding fraction forms Ca2+ channels in planar lipid bilayers. In: Plant membrane transport: The current position, pp. 277–278, Dainty, J., De Michaelis, M.I., Marre, E., Rasi-Caldogno, F., eds. Elsevier, Amsterdam

    Google Scholar 

  • Thuleau, P., Graziana, A., Canut, H., Ranjeva, R. (1990) A 75-kDa polypeptide, located primarily at the plasma membrane of carrot cell-suspension cultures, is photoaffmity labeled by the calcium channel blocker LU 49888. Proc. Natl. Acad. Sci. USA 87, 10000–10004

    Google Scholar 

  • Thuleau, P., Graziana, A., Ranjeva, R., Schroeder, J.I. (1993) Solubilized proteins from carrot (Daucus carota L.) membranes bind calcium channel blockers and form calcium-permeable ion channels. Proc. Natl. Acad. Sci. USA 90, 765–769

    Google Scholar 

  • White, P.J. (1993) Characterization of a high-conductance, voltage-dependent cation channel from the plasma membrane of rye roots in planar lipid bilayers. Planta 191, 541–551

    Google Scholar 

  • White, P.J., Tester, M. (1992) Potassium channels from plasma membrane of rye roots characterized following incorporation into planar bilayers. Planta 186, 188–202

    Google Scholar 

  • Zherelova, O.M. (1985) The necessity of ATP and Mg2+ for maintenance of the functional activity of calcium channels of Charophyta algae. Dokl. Biophys. 281, 37–39

    Google Scholar 

  • Zherelova, O.M. (1989a) Protein kinase C is involved in regulation of Ca2+ channels in plasmalemma of Nitella syncarpa. FEBS Lett. 242, 330–332

    Google Scholar 

  • Zherelova, O.M. (1989b) Ca2+ channels in Nitellopsis obtusa (Characeae) cell plasmalemma and regulation of their activity. Comp. Biochem. Physiol. 94A, 141–145

    Google Scholar 

  • Zherelova, O.M., Kataev, A.A., Berestovsky, G.N. (1987) Regulation of the calcium channels of the plasmalemma of Nitellopsis obtusa by intracellular calcium. Biophysics 32, 379–380

    Google Scholar 

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Correspondence to M. Tester.

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We wish to thank Dr. Christa Niemietz, Dr. Robert Reid and Prof. Andrew Smith for valuable discussions. This work was supported by the Australian Research Council and an OPRS award to M.P.

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Piñeros, M., Tester, M. Characterization of a voltage-dependent Ca2+-selective channel from wheat roots. Planta 195, 478–488 (1995). https://doi.org/10.1007/BF00195704

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