Skip to main content
The Plant Cell logoLink to The Plant Cell
. 1994 May;6(5):685–694. doi: 10.1105/tpc.6.5.685

Two Voltage-Gated, Calcium Release Channels Coreside in the Vacuolar Membrane of Broad Bean Guard Cells.

G J Allen 1, D Sanders 1
PMCID: PMC160468  PMID: 12244254

Abstract

Voltage-gated, Ca2+ release channels have been characterized at the vacuolar membrane of broad bean guard cells using patch clamps of excised, inside-out membrane patches. The most prevalent Ca2+ release channel had a conductance of 27 pS over voltages negative of the reversal potential (Erev) (cytosol referenced to vacuole), with 5,10, or 20 mM Ca2+ as the charge carrier on the vacuolar side and 50 mM K+ on the cytosolic side. The single-channel current saturated at ~2.6 pA. The relative permeability of the channel was in the range of a Pca2+:Pk+ ratio of 6:1. Divalent cations could act as charge carriers on the vacuolar side with a conductance series of Ba2+ > Mg2+ > Sr2+ > Ca2+ and a selectivity sequence of Ca2+ [approximately equals to] Ba2+ [approximately equals to] Sr2+ > Mg2+. The channel was gated open by cytosol-negative (physiological) transmembrane voltages, increases in vacuolar Ca2+ concentration, and increases in the vacuolar pH. The channel was potently inhibited by the Ca2+ channel blockers Gd3+ (half-maximal inhibition at 10.3 [mu]M) and nifedipine (half-maximal inhibition at 77 [mu]M). The stilbene derivative 4,4[prime]-diisothiocyano-2,2[prime]-stilbene disulfonate was also inhibitory (half-maximal inhibition for a 4-min incubation period at 6.3[mu]M). The 27-pS channel coresides in individual guard cell vacuoles with a less frequently observed 14-pS Ca2+ release channel that had similar, although not identical, voltage dependence and gating characteristics and a lower selectivity for Ca2+ over K+. The requirement for two channels with a similar function at the vacuolar membrane of guard cells is discussed.

Full Text

The Full Text of this article is available as a PDF (781.8 KB).

Selected References

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

  1. Barry P. H., Lynch J. W. Liquid junction potentials and small cell effects in patch-clamp analysis. J Membr Biol. 1991 Apr;121(2):101–117. doi: 10.1007/BF01870526. [DOI] [PubMed] [Google Scholar]
  2. Bertl A., Blumwald E., Coronado R., Eisenberg R., Findlay G., Gradmann D., Hille B., Köhler K., Kolb H. A., MacRobbie E. Electrical measurements on endomembranes. Science. 1992 Nov 6;258(5084):873–874. doi: 10.1126/science.1439795. [DOI] [PubMed] [Google Scholar]
  3. Brosnan J. M., Sanders D. Identification and Characterization of High-Affinity Binding Sites for Inositol Trisphosphate in Red Beet. Plant Cell. 1993 Aug;5(8):931–940. doi: 10.1105/tpc.5.8.931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cosgrove D. J., Hedrich R. Stretch-activated chloride, potassium, and calcium channels coexisting in plasma membranes of guard cells of Vicia faba L. Planta. 1991 Dec;186(1):143–153. doi: 10.1007/BF00201510. [DOI] [PubMed] [Google Scholar]
  5. FATT P., GINSBORG B. L. The ionic requirements for the production of action potentials in crustacean muscle fibres. J Physiol. 1958 Aug 6;142(3):516–543. doi: 10.1113/jphysiol.1958.sp006034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fairley-Grenot K. A., Assmann S. M. Permeation of Ca2+ through K+ channels in the plasma membrane of Vicia faba guard cells. J Membr Biol. 1992 Jun;128(2):103–113. doi: 10.1007/BF00231883. [DOI] [PubMed] [Google Scholar]
  7. Gelli A., Blumwald E. Calcium Retrieval from Vacuolar Pools (Characterization of a Vacuolar Calcium Channel). Plant Physiol. 1993 Aug;102(4):1139–1146. doi: 10.1104/pp.102.4.1139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gilroy S., Fricker M. D., Read N. D., Trewavas A. J. Role of Calcium in Signal Transduction of Commelina Guard Cells. Plant Cell. 1991 Apr;3(4):333–344. doi: 10.1105/tpc.3.4.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gilroy S., Read N. D., Trewavas A. J. Elevation of cytoplasmic calcium by caged calcium or caged inositol triphosphate initiates stomatal closure. Nature. 1990 Aug 23;346(6286):769–771. doi: 10.1038/346769a0. [DOI] [PubMed] [Google Scholar]
  10. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  11. Lemtiri-Chlieh F., MacRobbie E. A. Role of calcium in the modulation of Vicia guard cell potassium channels by abscisic acid: a patch-clamp study. J Membr Biol. 1994 Jan;137(2):99–107. doi: 10.1007/BF00233479. [DOI] [PubMed] [Google Scholar]
  12. Maathuis F. J., Sanders D. Plant membrane transport. Curr Opin Cell Biol. 1992 Aug;4(4):661–669. doi: 10.1016/0955-0674(92)90087-s. [DOI] [PubMed] [Google Scholar]
  13. McAinsh M. R., Brownlee C., Hetherington A. M. Visualizing Changes in Cytosolic-Free Ca2+ during the Response of Stomatal Guard Cells to Abscisic Acid. Plant Cell. 1992 Sep;4(9):1113–1122. doi: 10.1105/tpc.4.9.1113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Pantoja O., Gelli A., Blumwald E. Voltage-dependent calcium channels in plant vacuoles. Science. 1992 Mar 20;255(5051):1567–1570. doi: 10.1126/science.255.5051.1567. [DOI] [PubMed] [Google Scholar]
  15. Schroeder J. I., Hagiwara S. Repetitive increases in cytosolic Ca2+ of guard cells by abscisic acid activation of nonselective Ca2+ permeable channels. Proc Natl Acad Sci U S A. 1990 Dec;87(23):9305–9309. doi: 10.1073/pnas.87.23.9305. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Plant Cell are provided here courtesy of Oxford University Press

RESOURCES