Abstract
The slowly activating vacuolar (SV) channel of plant vacuoles is gated open by cytosolic free Ca2+ and by cytosol-positive potentials. Using vacuoles isolated from broad bean guard cell protoplasts, SV-mediated currents could be measured in the whole-vacuole configuration of a patch clamp as the time-dependent increase in current at cytosol-positive voltages. Time-dependent deactivation of the SV currents when changing from activating to nonactivating voltages (tail currents) was used to calculate the selectivity of the channel to Ca2+ and Cl- with respect to K+. Changing the equilibrium potential for each permeant ion (Ca2+, Cl-, and K+) at least once for individual vacuoles allowed the relative permeabilities (P) of each of these ions to be calculated in a single experiment. The resulting Pca:Pcl:Pk ratio was close to 3:0.1:1. In accord with its characterization as a weakly selective Ca2+ channel, the SV-mediated current density decreased with increasing Ca2+ activity in the vacuole lumen. SV currents were potently modulated by the Ca2+-dependent, calmodulin-stimulated protein phosphatase 2B (calcineurin). At low concentrations ([less than or equal to]0.4 units per mL), calcineurin stimulated SV currents by ~60%, whereas at higher concentrations the phosphatase was inhibitory, reaching ~90% inhibition at 3 units per mL. Bovine calmodulin had no direct effect on SV-mediated currents, although calcineurin stimulated by exogenous calmodulin inhibited SV currents at all concentrations tested with half-maximal inhibition for calcineurin at 0.16 units per mL. The inhibitory effect of calcineurin could be blocked by the pyrethroid deltamethrin, indicating inhibition of SV channels by calcineurin via dephosphorylation. A model is discussed in which vacuolar Ca2+ release through SV channels is subject to both positive feedforward and negative feedback control through cytosolic Ca2+ and dephosphorylation, respectively.
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- Allen G. J., Muir S. R., Sanders D. Release of Ca2+ from individual plant vacuoles by both InsP3 and cyclic ADP-ribose. Science. 1995 May 5;268(5211):735–737. doi: 10.1126/science.7732384. [DOI] [PubMed] [Google Scholar]
- Allen G. J., Sanders D. Two Voltage-Gated, Calcium Release Channels Coreside in the Vacuolar Membrane of Broad Bean Guard Cells. Plant Cell. 1994 May;6(5):685–694. doi: 10.1105/tpc.6.5.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Bertl A., Gradmann D., Slayman C. L. Calcium- and voltage-dependent ion channels in Saccharomyces cerevisiae. Philos Trans R Soc Lond B Biol Sci. 1992 Oct 29;338(1283):63–72. doi: 10.1098/rstb.1992.0129. [DOI] [PubMed] [Google Scholar]
- Bertl A., Slayman C. L. Complex modulation of cation channels in the tonoplast and plasma membrane of Saccharomyces cerevisiae: single-channel studies. J Exp Biol. 1992 Nov;172:271–287. doi: 10.1242/jeb.172.1.271. [DOI] [PubMed] [Google Scholar]
- Bethke P. C., Jones R. L. Ca2+-Calmodulin Modulates Ion Channel Activity in Storage Protein Vacuoles of Barley Aleurone Cells. Plant Cell. 1994 Feb;6(2):277–285. doi: 10.1105/tpc.6.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bowler C., Chua N. H. Emerging themes of plant signal transduction. Plant Cell. 1994 Nov;6(11):1529–1541. doi: 10.1105/tpc.6.11.1529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen P., Cohen P. T. Protein phosphatases come of age. J Biol Chem. 1989 Dec 25;264(36):21435–21438. [PubMed] [Google Scholar]
- Cohen P. The structure and regulation of protein phosphatases. Annu Rev Biochem. 1989;58:453–508. doi: 10.1146/annurev.bi.58.070189.002321. [DOI] [PubMed] [Google Scholar]
- Gilroy S., Bethke P. C., Jones R. L. Calcium homeostasis in plants. J Cell Sci. 1993 Oct;106(Pt 2):453–461. doi: 10.1242/jcs.106.2.453. [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]
- Hedrich R., Kurkdjian A. Characterization of an anion-permeable channel from sugar beet vacuoles: effect of inhibitors. EMBO J. 1988 Dec 1;7(12):3661–3666. doi: 10.1002/j.1460-2075.1988.tb03247.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li W., Luan S., Schreiber S. L., Assmann S. M. Evidence for protein phosphatase 1 and 2A regulation of K+ channels in two types of leaf cells. Plant Physiol. 1994 Nov;106(3):963–970. doi: 10.1104/pp.106.3.963. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Luan S., Albers M. W., Schreiber S. L. Light-regulated, tissue-specific immunophilins in a higher plant. Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):984–988. doi: 10.1073/pnas.91.3.984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meyer K., Leube M. P., Grill E. A protein phosphatase 2C involved in ABA signal transduction in Arabidopsis thaliana. Science. 1994 Jun 3;264(5164):1452–1455. doi: 10.1126/science.8197457. [DOI] [PubMed] [Google Scholar]
- Neher E. Correction for liquid junction potentials in patch clamp experiments. Methods Enzymol. 1992;207:123–131. doi: 10.1016/0076-6879(92)07008-c. [DOI] [PubMed] [Google Scholar]
- Poole R. J. Cellular signaling machinery: conservation from plant stomata to lymphocytes. Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3125–3126. doi: 10.1073/pnas.90.8.3125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Price A. H., Taylor A., Ripley S. J., Griffiths A., Trewavas A. J., Knight M. R. Oxidative Signals in Tobacco Increase Cytosolic Calcium. Plant Cell. 1994 Sep;6(9):1301–1310. doi: 10.1105/tpc.6.9.1301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosenberg R. L., Chen X. H. Characterization and localization of two ion-binding sites within the pore of cardiac L-type calcium channels. J Gen Physiol. 1991 Jun;97(6):1207–1225. doi: 10.1085/jgp.97.6.1207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward J. M., Schroeder J. I. Calcium-Activated K+ Channels and Calcium-Induced Calcium Release by Slow Vacuolar Ion Channels in Guard Cell Vacuoles Implicated in the Control of Stomatal Closure. Plant Cell. 1994 May;6(5):669–683. doi: 10.1105/tpc.6.5.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weiser T., Bentrup F. W. Pharmacology of the SV channel in the vacuolar membrane of Chenopodium rubrum suspension cells. J Membr Biol. 1993 Oct;136(1):43–54. doi: 10.1007/BF00241488. [DOI] [PubMed] [Google Scholar]
