Abstract
Intracellular microelectrode recordings and a two-electrode voltage clamp have been used to characterize the current carried by inward rectifying K+ channels of stomatal guard cells from the broadbean, Vicia faba L. Superficially, the current displayed many features common to inward rectifiers of neuromuscular and egg cell membranes. In millimolar external K+ concentrations (Ko+), it activated on hyperpolarization with half-times of 100-200 ms, showed no evidence of time- or voltage-dependent inactivation, and deactivated rapidly (tau approximately 10 ms) on clamping to 0 mV. Steady-state conductance- voltage characteristics indicated an apparent gating charge of 1.3-1.6. Current reversal showed a Nernstian dependence on Ko+ over the range 3- 30 mM, and the inward rectifier was found to be highly selective for K+ over other monovalent cations (K+ greater than Rb+ greater than Cs+ much greater than Na+). Unlike the inward rectifiers of animal membranes, the current was blocked by charybdotoxin and alpha- dendrotoxin (Kd much less than 50 nM), as well as by tetraethylammonium chloride (K1/2 = 9.1 mM); gating of the guard cell K+ current was fixed to voltages near -120 mV, independent of Ko+, and the current activated only with supramillimolar K+ outside (EK+ greater than -120 mV). Most striking, however, was inward rectifier sensitivity to [H+] with the K+ current activated reversibly by mild acid external pH. Current through the K+ inward rectifier was found to be largely independent of intracellular pH and the current reversal (equilibrium) potential was unaffected by pHo from 7.4 to 5.5. By contrast, current through the K+ outward rectifier previously characterized in these cells (1988. J. Membr. Biol. 102:235) was largely insensitive to pHo, but was blocked reversibly by acid-going intracellular pH. The action of pHo on the K+ inward rectifier could not be mimicked by extracellular Ca2+ for which changes in activation, deactivation, and conductance were consonant with an effect on surface charge ([Ca2+] less than or equal to 1 mM). Rather, extracellular pH affected activation and deactivation kinetics disproportionately, with acid-going pHo raising the K+ conductance and shifting the conductance-voltage profile positive-going along the voltage axis and into the physiological voltage range. Voltage and pH dependencies for gating were consistent with a single, titratable group (pKa approximately 7 at -200 mV) residing deep within the membrane electric field and accessible from the outside.(ABSTRACT TRUNCATED AT 400 WORDS)
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- Armstrong C. M., Lopez-Barneo J. External calcium ions are required for potassium channel gating in squid neurons. Science. 1987 May 8;236(4802):712–714. doi: 10.1126/science.2437654. [DOI] [PubMed] [Google Scholar]
- Begenisich T., Danko M. Hydrogen ion block of the sodium pore in squid giant axons. J Gen Physiol. 1983 Nov;82(5):599–618. doi: 10.1085/jgp.82.5.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blatt M. R., Beilby M. J., Tester M. Voltage dependence of the Chara proton pump revealed by current-voltage measurement during rapid metabolic blockade with cyanide. J Membr Biol. 1990 Apr;114(3):205–223. doi: 10.1007/BF01869215. [DOI] [PubMed] [Google Scholar]
- Blatt M. R., Thiel G., Trentham D. R. Reversible inactivation of K+ channels of Vicia stomatal guard cells following the photolysis of caged inositol 1,4,5-trisphosphate. Nature. 1990 Aug 23;346(6286):766–769. doi: 10.1038/346766a0. [DOI] [PubMed] [Google Scholar]
- Bush D. S., McColl J. G. Mass-Action Expressions of Ion Exchange Applied to Ca, H, K, and Mg Sorption on Isolated Cells Walls of Leaves from Brassica oleracea. Plant Physiol. 1987 Sep;85(1):247–260. doi: 10.1104/pp.85.1.247. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christensen O., Zeuthen T. Maxi K+ channels in leaky epithelia are regulated by intracellular Ca2+, pH and membrane potential. Pflugers Arch. 1987 Mar;408(3):249–259. doi: 10.1007/BF02181467. [DOI] [PubMed] [Google Scholar]
- Cook D. L., Ikeuchi M., Fujimoto W. Y. Lowering of pHi inhibits Ca2+-activated K+ channels in pancreatic B-cells. Nature. 1984 Sep 20;311(5983):269–271. doi: 10.1038/311269a0. [DOI] [PubMed] [Google Scholar]
- Eisenman G., Horn R. Ionic selectivity revisited: the role of kinetic and equilibrium processes in ion permeation through channels. J Membr Biol. 1983;76(3):197–225. doi: 10.1007/BF01870364. [DOI] [PubMed] [Google Scholar]
- FRANKENHAEUSER B., HODGKIN A. L. The action of calcium on the electrical properties of squid axons. J Physiol. 1957 Jul 11;137(2):218–244. doi: 10.1113/jphysiol.1957.sp005808. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gehring C. A., Irving H. R., Parish R. W. Effects of auxin and abscisic acid on cytosolic calcium and pH in plant cells. Proc Natl Acad Sci U S A. 1990 Dec 15;87(24):9645–9649. doi: 10.1073/pnas.87.24.9645. [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]
- HODGKIN A. L., HUXLEY A. F., KATZ B. Measurement of current-voltage relations in the membrane of the giant axon of Loligo. J Physiol. 1952 Apr;116(4):424–448. doi: 10.1113/jphysiol.1952.sp004716. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Miyazaki S., Moody W., Patlak J. Blocking effects of barium and hydrogen ions on the potassium current during anomalous rectification in the starfish egg. J Physiol. 1978 Jun;279:167–185. doi: 10.1113/jphysiol.1978.sp012338. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Miyazaki S., Rosenthal N. P. Potassium current and the effect of cesium on this current during anomalous rectification of the egg cell membrane of a starfish. J Gen Physiol. 1976 Jun;67(6):621–638. doi: 10.1085/jgp.67.6.621. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hagiwara S., Yoshii M. Effects of internal potassium and sodium on the anomalous rectification of the starfish egg as examined by internal perfusion. J Physiol. 1979 Jul;292:251–265. doi: 10.1113/jphysiol.1979.sp012849. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartung W., Radin J. W., Hendrix D. L. Abscisic Acid Movement into the Apoplastic solution of Water-Stressed Cotton Leaves: Role of Apoplastic pH. Plant Physiol. 1988 Mar;86(3):908–913. doi: 10.1104/pp.86.3.908. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hedrich R., Busch H., Raschke K. Ca2+ and nucleotide dependent regulation of voltage dependent anion channels in the plasma membrane of guard cells. EMBO J. 1990 Dec;9(12):3889–3892. doi: 10.1002/j.1460-2075.1990.tb07608.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hille B. Potassium channels in myelinated nerve. Selective permeability to small cations. J Gen Physiol. 1973 Jun;61(6):669–686. doi: 10.1085/jgp.61.6.669. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hille B., Woodhull A. M., Shapiro B. I. Negative surface charge near sodium channels of nerve: divalent ions, monovalent ions, and pH. Philos Trans R Soc Lond B Biol Sci. 1975 Jun 10;270(908):301–318. doi: 10.1098/rstb.1975.0011. [DOI] [PubMed] [Google Scholar]
- MacKinnon R., Miller C. Mutant potassium channels with altered binding of charybdotoxin, a pore-blocking peptide inhibitor. Science. 1989 Sep 22;245(4924):1382–1385. doi: 10.1126/science.2476850. [DOI] [PubMed] [Google Scholar]
- Majernik O., Mansfield T. A. Direct effect of SO2 pollution on the degree of opening of stomata. Nature. 1970 Jul 25;227(5256):377–378. doi: 10.1038/227377a0. [DOI] [PubMed] [Google Scholar]
- Moczydlowski E., Lucchesi K., Ravindran A. An emerging pharmacology of peptide toxins targeted against potassium channels. J Membr Biol. 1988 Oct;105(2):95–111. doi: 10.1007/BF02009164. [DOI] [PubMed] [Google Scholar]
- Moody W. J., Hagiwara S. Block of inward rectification by intracellular H+ in immature oocytes of the starfish Mediaster aequalis. J Gen Physiol. 1982 Jan;79(1):115–130. doi: 10.1085/jgp.79.1.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moody W., Jr Effects of intracellular H+ on the electrical properties of excitable cells. Annu Rev Neurosci. 1984;7:257–278. doi: 10.1146/annurev.ne.07.030184.001353. [DOI] [PubMed] [Google Scholar]
- Neyton J., Pelleschi M. Multi-ion occupancy alters gating in high-conductance, Ca(2+)-activated K+ channels. J Gen Physiol. 1991 Apr;97(4):641–665. doi: 10.1085/jgp.97.4.641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ohmori H. Inactivation kinetics and steady-state current noise in the anomalous rectifier of tunicate egg cell membranes. J Physiol. 1978 Aug;281:77–99. doi: 10.1113/jphysiol.1978.sp012410. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodriguez-Navarro A., Blatt M. R., Slayman C. L. A potassium-proton symport in Neurospora crassa. J Gen Physiol. 1986 May;87(5):649–674. doi: 10.1085/jgp.87.5.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saftner R. A., Raschke K. Electrical potentials in stomatal complexes. Plant Physiol. 1981 Jun;67(6):1124–1132. doi: 10.1104/pp.67.6.1124. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanders D., Slayman C. L. Control of intracellular pH. Predominant role of oxidative metabolism, not proton transport, in the eukaryotic microorganism Neurospora. J Gen Physiol. 1982 Sep;80(3):377–402. doi: 10.1085/jgp.80.3.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schroeder J. I. K+ transport properties of K+ channels in the plasma membrane of Vicia faba guard cells. J Gen Physiol. 1988 Nov;92(5):667–683. doi: 10.1085/jgp.92.5.667. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schroeder J. I., Raschke K., Neher E. Voltage dependence of K channels in guard-cell protoplasts. Proc Natl Acad Sci U S A. 1987 Jun;84(12):4108–4112. doi: 10.1073/pnas.84.12.4108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schweitz H., Stansfeld C. E., Bidard J. N., Fagni L., Maes P., Lazdunski M. Charybdotoxin blocks dendrotoxin-sensitive voltage-activated K+ channels. FEBS Lett. 1989 Jul 3;250(2):519–522. doi: 10.1016/0014-5793(89)80788-4. [DOI] [PubMed] [Google Scholar]
- Standen N. B., Stanfield P. R. Potassium depletion and sodium block of potassium currents under hyperpolarization in frog sartorius muscle. J Physiol. 1979 Sep;294:497–520. doi: 10.1113/jphysiol.1979.sp012943. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waddell W. J., Bates R. G. Intracellular pH. Physiol Rev. 1969 Apr;49(2):285–329. doi: 10.1152/physrev.1969.49.2.285. [DOI] [PubMed] [Google Scholar]
- Wagner R., Apley E. C., Hanke W. Single channel H+ currents through reconstituted chloroplast ATP synthase CF0-CF1. EMBO J. 1989 Oct;8(10):2827–2834. doi: 10.1002/j.1460-2075.1989.tb08429.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woodhull A. M. Ionic blockage of sodium channels in nerve. J Gen Physiol. 1973 Jun;61(6):687–708. doi: 10.1085/jgp.61.6.687. [DOI] [PMC free article] [PubMed] [Google Scholar]