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.
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]