Effects of cytosolic calcium and limited, possible dual, effects of G protein modulators on guard cell inward potassium channels
Article first published online: 17 FEB 2003
The Plant Journal
Volume 8, Issue 4, pages 479–489, October 1995
How to Cite
Kelly, W. B., Esser, J. E. and Schroeder, J. I. (1995), Effects of cytosolic calcium and limited, possible dual, effects of G protein modulators on guard cell inward potassium channels. The Plant Journal, 8: 479–489. doi: 10.1046/j.1365-313X.1995.8040479.x
- Issue published online: 17 FEB 2003
- Article first published online: 17 FEB 2003
- Received 27 February 1995; revised 16 June 1995; accepted 13 July 1995.
- Cited By
The cellular mechanisms that regulate potassium (K+) channels in guard cells have been the subject of recent research, as K+ channel modulation has been suggested to contribute to stomatal movements. Patch clamp studies have been pursued on guard cell protoplasts of Vicia faba to analyze the effects of physiological cytosolic free Ca2+ concentrations, Ca2+ buffers and GTP-binding protein modulators on inward-rectifying K+ channels. Ca2+ inhibition of inward-rectifying K+ currents depended strongly on the concentration and effectiveness of the Ca2+ buffer used, indicating a large Ca2+ buffering capacity and pH increases in guard calls. When the cytosolic Ca2+ concentration was buffered to micromolar levels using BAPTA, inward-rectifying K+ channels were strongly inhibited. However, when EGTA was used as the Ca2+ buffer, much less inhibition was observed, even when pipette solutions contained 1 µM free Ca2+. Under the imposed conditions, GTPγS did not significantly inhibit inward-rectifying K+ channel currents when cytosolic Ca2+ was buffered to low levels or when using EGTA as the Ca2+ buffer. Furthermore, GDPβS reduced inward K+ currents at low cytosolic Ca2+, indicating a novel mode of inward K+ channel regulation by G-protein modulators, which is opposite in effect to that from previous reports. On the other hand, when Ca2+ was effectively elevated in the cytosol to 1 µM using BAPTA, GTPγS produced an additional inhibition of the inward-rectifying K+ channel currents in a population of cells, indicating possible Ca2+-dependent action of GTP-binding protein modulators in K+ channel inhibition. Assays of stomatal opening show that 90% inhibition of inward K+ currents does not prohibit, but slows, stomatal opening and reduces stomatal apertures by only 34% after 2 h light exposure. These data suggest that limited K+ channel down-regulation alone may not be rate-limiting, and it is proposed that the concerted action of proton-pump inhibition and additional anion channel activation is likely required for inhibition of stomatal opening. Furthermore, G-protein modulators regulate inward K+ channels in a more complex and limited, possibly Ca2+-dependent, manner than previously proposed.