A transient outward-rectifying K+ channel current down-regulated by cytosolic Ca2+ in Arabidopsis thaliana guard cells

Sustained (noninactivating) outward-rectifying K+ channel currents have been identified in a variety of plant cell types and species. Here, in Arabidopsis thaliana guard cells, in addition to these sustained K+ currents, an inactivating outward-rectifying K+ current was characterized (plant A-type c...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1998-05, Vol.95 (11), p.6548-6553
Hauptverfasser: Pei, Z.M. (University of California, San Diego, La Jolla, CA.), Baizabal-Aguirre, V.M, Allen, G.J, Schroeder, J.I
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Sprache:eng
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Zusammenfassung:Sustained (noninactivating) outward-rectifying K+ channel currents have been identified in a variety of plant cell types and species. Here, in Arabidopsis thaliana guard cells, in addition to these sustained K+ currents, an inactivating outward-rectifying K+ current was characterized (plant A-type current:I(AP)). I(AP) activated rapidly with a time constant of 165 ms and inactivated slowly with a time constant of 7.2 sec at +40 mV. I(AP) was enhanced by increasing the duration (from 0 to 20 sec) and degree (from +20 to -100 mV) of prepulse hyperpolarization. Ionic substitution and relaxation (tail) current recordings showed that outward I(AP) was mainly carried by K+ ions. In contrast to the sustained outward-rectifying K+ currents, cytosolic alkaline pH pH was found to inhibit I(AP) and extracellular K+ was required for I(AP) activity. Furthermore, increasing cytosolic free Ca2+ in the physiological range strongly inhibited I(AP) activity with a half inhibitory concentration of approximately 94 nM. We present a detailed characterization of an inactivating K+ current in a higher plant cell. Regulation of I(AP) by diverse factors including membrane potential, cytosolic Ca2+ and pH, and extracellular K+ and Ca2+ implies that the inactivating I(AP) described here may have important functions during transient depolarizations found in guard cells, and in integrated transduction processes during stomatal movement
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.95.11.6548