Research ArticleCELL BIOLOGY AND SIGNAL TRANSDUCTION
Open Access

Phosphatidylinositol (4,5)Bisphosphate Inhibits K+-Efflux Channel Activity in NT1 Tobacco Cultured Cells

Xiaohong Ma, Oded Shor, Sofia Diminshtein, Ling Yu, Yang Ju Im, Imara Perera, Aaron Lomax, Wendy F. Boss, Nava Moran

Published February 2009. DOI: https://doi.org/10.1104/pp.108.129007

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Abstract

In the animal world, the regulation of ion channels by phosphoinositides (PIs) has been investigated extensively, demonstrating a wide range of channels controlled by phosphatidylinositol (4,5)bisphosphate (PtdInsP2). To understand PI regulation of plant ion channels, we examined the in planta effect of PtdInsP2 on the K+-efflux channel of tobacco (Nicotiana tabacum), NtORK (outward-rectifying K channel). We applied a patch clamp in the whole-cell configuration (with fixed “cytosolic” Ca2+ concentration and pH) to protoplasts isolated from cultured tobacco cells with genetically manipulated plasma membrane levels of PtdInsP2 and cellular inositol (1,4,5)trisphosphate: “Low PIs” had depressed levels of these PIs, and “High PIs” had elevated levels relative to controls. In all of these cells, K channel activity, reflected in the net, steady-state outward K+ currents (IK), was inversely related to the plasma membrane PtdInsP2 level. Consistent with this, short-term manipulations decreasing PtdInsP2 levels in the High PIs, such as pretreatment with the phytohormone abscisic acid (25 μm) or neutralizing the bath solution from pH 5.6 to pH 7, increased IK (i.e. NtORK activity). Moreover, increasing PtdInsP2 levels in controls or in abscisic acid-treated high-PI cells, using the specific PI-phospholipase C inhibitor U73122 (2.5–4 μm), decreased NtORK activity. In all cases, IK decreases stemmed largely from decreased maximum attainable NtORK channel conductance and partly from shifted voltage dependence of channel gating to more positive potentials, making it more difficult to activate the channels. These results are consistent with NtORK inhibition by the negatively charged PtdInsP2 in the internal plasma membrane leaflet. Such effects are likely to underlie PI signaling in intact plant cells.

Many environmental and internal signals induce increased metabolism of phosphoinositides (PIs) in both animal and plant cells. PIs are involved in numerous cellular processes important for cell development and growth, including secretion of metabolites, vesicular transport, organization of the cytoskeleton, and regulation of ion channels and transporters (for review, see Hilgemann, 2003; Meijer and Munnik, 2003; Suh and Hille, 2005; Huang, 2007). In many signaling cascades, phosphatidylinositol (4,5)bisphosphate (PtdInsP2) undergoes cleavage by phospholipase C (PLC), producing diacylglycerol and inositol (1,4,5)trisphosphate (InsP3). While diacylglycerol operates within the plane of the membrane, production of InsP3 is practically synonymous with further signaling through mobilization of Ca2+ from internal stores (Berridge and Irvine, 1984; Berridge et al., 1998).

In the last decade, signaling via PtdInsP2 itself, rather than via its cleavage products, has become the focus of intense study in animal cells. Detailed descriptions have accumulated about PtdInsP2 interactions with membrane ion channels and other ion transporters, highlighting its important roles in conveying information about physical and chemical stimuli and in maintaining cellular ionic homeostasis (for review, see Suh and Hille, 2005; Huang, 2007).

In the plant world, this topic has been evolving at a much slower pace. Over two decades of study focusing on plant signaling via the PI pathway and Ca2+ mobilization have linked signals that cause cell shrinking with the cleavage of PtdInsP2, for example, in the case of the phytohormone abscisic acid (ABA) in Vicia faba guard cells (Lee et al., 1996) or blue light in the leaf motor cells, such as “flexors” of Samanea saman (Kim et al., 1996) and “extensors” of Phaseolus coccineus (Mayer et al., 1997). Moreover, a strong positive correlation has been revealed between these “shrinking signals” and the activation of anion- and K+-release channels in the plasma membrane of the shrinking cells (Blatt, 2000; Suh et al., 2000; Hetherington, 2001; Schroeder et al., 2001; Moran, 2007a, 2007b; Pandey et al., 2007). Accumulating evidence dissociated the activation of these channels from obligatory Ca2+ mobilization, suggesting alternative signaling pathways: for example, Marten et al. (2007), using fluorescent Ca2+-reporter dye, demonstrated ABA activation of anion channels in V. faba and tobacco (Nicotiana tabacum) guard cells in the absence of or prior to an observable rise in cytosolic [Ca2+]. Similarly, Lemtiri-Chlieh and MacRobbie (1994) found in patch-clamp experiments with Ca2+-buffered cytosolic milieu that ABA activation of K+-release channels in V. faba guard cells was independent of cytosolic Ca2+. Importantly, and consistent with the latter report, direct examination of K+-release channels in excised membrane patches from V. faba guard cells (Hosoi et al., 1988) or from S. saman motor cells (Moshelion and Moran, 2000) revealed that their activity did not require Ca2+ at their cytosolic surface. Cytosolic alkalinization or membrane depolarization resulting from H+ pump inhibition and anion channel activation have been proposed as alternative mediators of ABA activation of guard cell K+-release channels (Irving et al., 1992; Macrobbie, 1992; Blatt and Armstrong, 1993; for a recent review, see Pandey et al., 2007). However, depolarization accounted only partially for the stimulation of K+-release channel activity by a “shrinking” blue light in the case of S. saman leaf motor cells (Suh et al., 2000).

Could PtdInsP2 itself modulate K+-release channels? To address this question, Liu et al. (2005) examined three plant K channels, two K+ influx channels, LKT1, a tomato (Solanum lycopersicum) homolog of the Arabidopsis (Arabidopsis thaliana) AKT1, the Arabidopsis KAT1, and the Arabidopsis K+-efflux channel, SKOR. Applying a patch clamp to frog oocytes expressing these channels, they demonstrated Ca2+-independent regulation by PI lipids. Isomers of PtdInsP, PtdInsP2, or PtdInsP3 applied to the cytosolic side of excised membrane patches prevented the rundown and enhanced the activity of these channels (Liu et al., 2005). These results, resembling direct activation of various types of animal ion channels by PtdIns(4,5)P2 (for review, see Hilgemann, 2004; Suh and Hille, 2005; Huang, 2007), suggested a direct correlation between PtdInsP2 level and SKOR activity in oocytes (Liu et al., 2005).

In contrast, interpretation of in planta experiments leads to a direct relation between the up-regulation of the K+-release channel and PtdInsP2 cleavage (i.e. to an inverse correlation between PtdInsP2 level in the membrane and channel activity). This can be seen in the case of SKOR-like channels in guard cells (Blatt, 1990; Blatt et al., 1990; Lemtiri-Chlieh and MacRobbie, 1994; Lemtiri-Chlieh, 1996) or in S. saman flexors (Kim et al., 1996; Suh et al., 2000).

To reconcile this apparent discrepancy, we undertook to examine this relationship more explicitly in planta. We investigated NtORK in tobacco cultured cells (NT1), the previously described representative of the SKOR-related K+-release channel family (Kasukabe et al., 2006; Sano et al., 2007, 2008). We used NT1 with genetically manipulated basal levels of PtdInsP2 and InsP3 (Perera et al., 2002; Im et al., 2007). Three types of cell lines were studied: “Low PIs,” cells with lowered (relative to controls) levels of PtdInsP2 and InsP3; “High PIs,” cells with elevated levels of both PIs; and control cell lines transformed with “empty” vectors and the wild type. Using a patch clamp in a whole-cell configuration, with the cytosolic concentrations of Ca2+ and protons tightly controlled by appropriate buffers, we established in these cells a negative correlation between the basal level of PtdInsP2 and NtORK activity, as expected from the reported plant motor cell findings. Further manipulations of the PtdInsP2 membrane levels, causing either its cleavage by the plant hormone ABA and by elevation of bath pH or its accumulation by PLC inhibition, strengthened this conclusion. Taken together, our results strongly suggest the inhibition of NtORK by PtdInsP2. In addition, the initiation of a signaling cascade by ABA in the NT1 cells, which is characteristic of guard cells, should further encourage the use of this model system in studies of signal transduction.

RESULTS

K+-Release Channels in Tobacco Cultured Cells with Modified Membrane Lipids

Channel Identification through Comparison with Previous Work

In whole-cell patch-clamp configuration, increasingly depolarizing voltage pulses evoked ion channel activity. This is evident in all protoplasts of the three types of NT1 cell lines, the Low PIs, the High PIs, and the various controls (Fig. 1A ; see “Materials and Methods”), as time-dependent outward currents. The sigmoidal time and voltage dependencies of these currents resembled those of outward K+ currents, flowing through K channels, described already in the similar tobacco cell line BY2 (Stoeckel and Takeda, 2002; Sano et al., 2007).

Figure 1.
Figure 1.

Comparison of steady-state and instantaneous currents in NT1 cells. A, Whole-cell currents (superimposed traces) evoked by a series of increasingly depolarizing voltage pulses in tobacco protoplasts with different membrane PI levels. WT (Wild type), one of the control cell lines with intermediate PI levels; Low PIs, cell line (I2-8) with diminished level of PIs; High PIs, cell line (HsPIPKlα-2) with elevated PI levels. Numbers to the right of traces or near leftward- or rightward-pointing arrows indicate the values of EM, membrane potential (in mV), during the recording. Black symbols indicate instantaneous currents, IO (leak), and white symbols indicate steady-state current values, which, after subtraction of corresponding IO, yield the net steady-state current, IK. Note the 2.7-s-long break in the time scale; the 0.05-s scale bar relates to the first part, and the 0.2-s scale bar relates to the second part, restarting about 2.9 s after beginning of the pulse (upward arrow). The inset shows the recording configuration. B, Membrane potential dependence of whole-cell current (so-called current-voltage, I-V or I-EM, relationship) obtained from the records, in A, of IK or IO, as indicated by the symbols. Prime (′) indicates normalization of the currents to the cell's capacitance (see “Materials and Methods”). Note the constant slope of I′O, indicating voltage-independent leak conductance, and its close-to-null reversal potential, indicating poor ion selectivity.

Channel Identification by Blockers

We identified the channels as K+-conducting channels by following treatments with the classical K channel blockers: (1) internal Cs+ to block the outward current (Supplemental Fig. S1A), (2) external Cs+ to block the inward “tail” current (Supplemental Fig. S1B), and (3) external Ba2+ to block both the outward and the inward currents (Supplemental Fig. S1C). Furthermore, in all of the cell lines, the reversal potentials of these currents were only slightly more depolarized than the calculated K+ equilibrium (Nernst) potential of −81 mV (Supplemental Fig. S2), providing additional support for identifying these channels as K+-selective K+-release channels, NtORK channels (Sano et al., 2007). Actually, although two genes, NtORK1 and NtORK2, have been mentioned in the literature, only NtORK1 has been characterized to some extent so far (Langer et al., 2002; Kasukabe et al., 2006; Sano et al., 2007). Because our measurements do not indicate clearly two separate types of channels, we use the inclusive name, NtORK.

Correlating Channel Activity with PtdInsP2 Level

At external pH 5.6, the NtORK channels were most active in the Low PIs, least active in the High PIs, and they displayed intermediate activity in the control protoplasts, as evident from the net, steady-state K+ currents normalized to cell capacitance, I′K (Fig. 1; Supplemental Fig. S3, A and B; see “Materials and Methods”). The effect of the InsP3 5-phosphatase with which the Low PIs were generated was evident in the cells where the 5-phosphatase was targeted to the plasma membrane (I2-8 and I4-2; Perera et al., 2002; Supplemental Fig. S4). When the 5-phosphatase was inactive (C348S) or missing the C terminus and therefore no longer bound to the plasma membrane (ΔC), the channels behaved similarly to the wild-type or “empty-vector” (C5, GFP) controls (Supplemental Fig. S3A). These data indicate that plasma membrane targeting, not just the ability to hydrolyze InsP3 (Supplemental Fig. S5), is essential. It is most likely that the InsP3 5-phosphatase needs to be in close proximity to the channel to have an effect.

In contrast to I′K, the baseline “leaks” (normalized instantaneous currents), I′O, were larger in the High PIs than in all other cells, but in all cell types, leak conductance was constant over the whole voltage range and its ion selectivity was poor. We base this latter conclusion on the linearity of the I′O-EM (current-membrane potential) curves and their nearly null intersection with the abscissa, which was an intermediate value between all equilibrium potentials calculated for the ions in the solutions on both sides of the membrane (Fig. 1; Supplemental Fig. S3, C and D).

Components of Channel Inhibition

In an attempt to resolve the possible effects of PtdInsP2 on NtORK into effects on properties of the open channel versus effects on channel gating (i.e. opening and closing), we examined the voltage dependence of its chord conductance, G′K, extracted from I′K (Eq. 1 in “Materials and Methods”). Three characteristic Boltzmann parameters served to compare the cell lines: G′max, the maximum attainable conductance (normalized to cell capacitance); E1/2, the voltage at which half of G′max is attained; and z, the effective charge of the gating subunits (Eq. 2 in “Materials and Methods”). As could be deduced from the current measurements, cells with higher PtdInsP2 levels had lower G′max, and vice versa (Fig. 2, A and B ). This analysis revealed also a mean difference of about 23 mV between E1/2 values of the High PIs and the rest of the cell lines. This difference is concealed in the I′K-EM plots (Supplemental Fig. S3, A and B) and even in the G′K-EM plots (Fig. 2A) and is clearly visible only in the plots of the probability of opening, PO, versus membrane potential (Eq. 3 in “Materials and Methods”). Thus, the PO-voltage relationships (PO-EMs) of the High PIs, reflecting the voltage dependence of the channel-gating subunits, were shifted significantly to more depolarizing membrane potentials (rightward) relative to Low PIs and controls (Fig. 2, B and C). z values, reflected in the “slopes” of the G′K-EM curves, did not vary among the three cell types (High PIs, Low PIs, and controls; Fig. 2B).

Figure 2.
Figure 2.

The effect of PtdInsP2 on the K channel chord conductance. A, Symbols show mean ± se conductance-voltage relationships normalized to cell capacitance (G′K-EMs), obtained by averaging individual G′K-EMs (G′K units: Siemens/Farad) extracted from each cell's I′K-EM relationships (see “Materials and Methods”). The chosen cell lines represent the Low PIs, High PIs, and controls shown in Supplemental Figure S3 and described in “Results” and “Materials and Methods.” The numbers of assayed cells are indicated in parentheses. Lines were calculated using Equation 2 and the averaged best-fit Boltzmann parameters (G′max, E1/2, z; shown in B) obtained from analyses of individual G′K-EMs. WT, Wild type. B, Mean ± se best-fit Boltzmann parameters resulting from fitting Equation 2 to the individual G′K-EMs of cells in A (see “Materials and Methods”): G′max, the maximum (asymptotic) conductance (top panel); E1/2, the EM value at half-G′max (middle panel); and z, the effective charge of the gating subunit (bottom panel). The parameter values differ significantly if they are denoted by different letters (a, b, or c). Other details are as in A. C, Symbols show mean ± se probability of channel opening versus voltage, PO-EM, relationships. Lines are as in A, except for using Equation 3 here. Vertical dashed lines and arrows denote the corresponding E1/2 values.

Effects of ABA

Effects of ABA on Plasma Membrane PtdInsP2 Content

If indeed NtORK activity depends inversely on the membrane PtdInsP2 content, lowering the PtdInsP2 level should increase NtORK activity. Therefore, we examined whether we can lower the PtdInsP2 in the high-PI NT1 cells utilizing the plant hormone ABA, which is known to activate PLC in guard cells (Lee et al., 1996). Indeed, a 15-min incubation of protoplasts isolated from the high-PI cells with 25 μm ABA significantly lowered the PtdInsP2 levels (Fig. 3 ). The mean effects of ABA on the already low levels of PtdInsP2 present in wild-type cells were minute, and in the GFP cells they were insignificant.

Figure 3.
Figure 3.

The effect of ABA on PtdInsP2 levels in the plasma membrane (PM). Mean ± sd of PtdInsP2 levels in protoplasts isolated from the indicated cell lines, incubated for 15 min without and with 25 μm ABA at a temperature of 24°C to 25°C. Plasma membrane lipid levels were determined based on an InsP3 assay of the lipid hydrolysate (Im et al., 2007; see “Materials and Methods”). The results shown are from one of two independent experiments performed with two replicates that gave similar results. WT, Wild type.

Effects of ABA on NtORK

In the patch-clamp experiments, 10- to 20-min preincubation of protoplast with 25 μm ABA increased I′K in the High PIs and had no effect on I′K in the control cell lines (Fig. 4A ). This correlated with changes in the PtdInsP2 levels. Boltzmann analysis of NtORK G′K revealed that in the High PIs, but not in the controls, ABA pretreatment increased G′max considerably and shifted E1/2 by about 15 mV in a hyperpolarizing (leftward) direction (Fig. 5 ). z was not affected by ABA (Fig. 5B).

Figure 4.
Figure 4.

The effect of ABA on I′K and leak current. A, Mean ± se normalized net steady-state K+ current-voltage (I′K-EM) relationships in High PIs (HsPIPKIα-2 and HsPIPKIα-3) and their controls (wild type [WT] and GFP). The numbers of assayed cells are indicated in parentheses. Round arrows indicate the effect of ABA. B, Normalized instantaneous currents, leak voltage (I′O-EM) relationships in High PIs and in their controls with and without ABA, obtained from the same current records as those used for A. Round arrows are as in A. ABA decreased I′O significantly only in one high-PI line.

Figure 5.
Figure 5.

The effects of ABA on the K channel chord conductance. A, Symbols show mean ± se G′K-EM relations of the cells in Figure 4A (data of both high-PI cell lines were pooled together for the presentation). Lines were calculated using Equation 2 and the averaged best-fit Boltzmann parameters (G′max, E1/2, z; shown in B) obtained from analyses of individual G′K-EMs. B, Mean ± se best-fit Boltzmann parameters. The parameter values differ significantly if they are denoted by different letters (a or b). C, Symbols show mean ± se probability of channel opening, PO-EM, relationships. Data of both cell lines were pooled together as in A. Lines are as in A, except for using Equation 3 here. Vertical dashed lines and arrows denote E1/2 values without (right) and with (left) ABA. Note the ABA-induced hyperpolarizing shift of PO-EM.

Effects of pH

Effects of pH on the Content of Plasma Membrane PtdInsP2

Because a small alkalinization of the apoplast was correlated with stomatal closure in Vicia faba and potato (Solanum tuberosum) leaves (Hedrich et al., 2001), we hypothesized that pH would have an ABA-mimicking (although ABA-independent) effect. Incubating the wild-type cells for about 15 min in external solution buffered to pH 7.0 (rather than to pH 5.5) decreased the plasma membrane PtdInsP2 levels only by roughly 10 units (pmol min−1 mg−1 plasma membrane protein), and in GFP cells the mean PtdInsP2 level was not affected (Fig. 6 ). In contrast, in high-PI protoplasts, the pH shift decreased the PtdInsP2 levels by about 100 to 440 units (Fig. 6), resembling the effect of ABA (Fig. 3).

Figure 6.
Figure 6.

The effect of protons on PtdInsP2 levels. Mean (±sd) PtdInsP2 levels in protoplasts isolated from the indicated cell lines, incubated for 15 min at pH 5.5 and pH 7 at a temperature of 24°C to 25°C. Lipid levels were determined as described in the Figure 3 legend. The control values are those of Figure 3. The results shown are from one of two independent experiments performed with two replicates. PM, Plasma membrane; WT, wild type.

Effects of pH on NtORK

In correlation to the effect of pH on PtdInsP2 levels, 10- to 20-min incubation of protoplasts in the external solution buffered to pH 7 prior to attaining a whole-cell patch-clamp configuration increased I′K in the High PIs but did not affect I′K in the control cell line (Fig. 7A ). Boltzmann analysis of NtORK G′K-EM relationships (Fig. 8 ) revealed an increase of the maximum conductance, G′max (Fig. 8, A and B) and a hyperpolarizing (leftward) shift of about 36 mV of the PO-EM relationship (Fig. 8, B and C). In contrast to enhancing I′K (i.e. NtORK activity), pH 7 significantly decreased the leak currents in both High PIs, down to its levels in the control cells (Fig. 7B).

Figure 7.
Figure 7.

The effects of pH 7 on I′K and leak current. A, Mean ± se I′K-EM relationships of the High PIs and their control, GFP. Round arrows indicate the effect of pH neutralization. The numbers of assayed cells are indicated in parentheses. B, Mean ± se I′O-EM relationships in High PIs and the GFP control obtained from the same current records as the data of A. Round arrows are as in A.

Figure 8.
Figure 8.

The effects of pH 7 on the K channel chord conductance. A, Symbols show mean ± se G′K-EM relations of the cells in Figure 7. Data of both high-PI cell lines were pooled together for clarity. Lines were calculated using Equation 2 and the averaged best-fit Boltzmann parameters (G′max, E1/2, z; shown in B) obtained from analyses of individual G′K-EMs. B, Mean ± se best-fit Boltzmann parameters. The parameter values differ significantly if they are denoted by different letters (a or b). Numbers inside columns are the numbers of cells contributing to the averages. C, Symbols show mean ± se PO-EM relationships. Data of both high-PI cell lines were pooled together for clarity. Lines are as in A, except for using Equation 3 here. Vertical dashed lines and arrows denote E1/2 values at pH 5.6 (right) and at pH 7 (left). Note the pH neutralization-induced hyperpolarizing shift of PO-EM of the High PIs.

Effects of PLC Inhibitor

If PtdInsP2 inhibits NtORK activation, then preventing its cleavage by inhibiting PLC, consequently leading to PtdInsP2 accumulation, should decrease NtORK conductance. In ABA-pretreated protoplasts from High PIs (to promote their NtORK activity) or in wild-type protoplasts, a bath exposure to U73122 (the commonly used PI-PLC inhibitor; Bleasdale et al., 1990) decreased I′K progressively within a few minutes (Fig. 9 ). Adding the same volume of the external solution to the bath with the High PIs or adding U73343, the inactive analog of U73122 (Bleasdale et al., 1990), to wild-type protoplasts had no immediate discernible effect on I′K (Fig. 9, B and D). Longer term incubation of control cell protoplasts with U73122 (including several minutes prior to attaining the whole-cell configuration) resulted, on average, in about 65% inhibition of I′K; however, the same treatment with U73343 inhibited I′K by only about 20% (Fig. 10A ). U73122 also decreased I′O, while U73343 did not affect it (Fig. 10B).

Figure 9.
Figure 9.

The effect of U73122. Superimposed traces of membrane currents recorded in a whole-cell patch-clamp configuration, elicited by depolarizing pulses to +85 mV applied repeatedly every 30 s from a holding potential of −70 mV. A, High-PI cells (HsPIPKIα-2) preincubated with 25 μm ABA prior to beginning the recording, then exposed to 5 μL of plain external solution added to the bath and, subsequently, to 5 μL of 250 μm U73122, to a final concentration of approximately 4 μm. The arrowhead indicates the holding current at −70 mV. B, Time course of I′K during the experiment in A. Vertical arrows show timing of treatments. C, An experiment similar to A, using control wild-type (WT) protoplasts without preincubation (the traces were shifted slightly to superimpose at the holding current). U73343, the inactive analog of U73122, and then U73122 were added, as in A, each to a final concentration of 4 μm. The other details are similar to those in A. D, Time course of I′K during the experiment in C. Two representatives of four similar independent experiments are shown.

Figure 10.
Figure 10.

Steady-state effect of U73122 on NtORK conductance. Protoplasts of the control line C-5 (see “Materials and Methods”) were exposed to U73122 or U73343 in the bath (2.5 μm) starting about 3 min prior to attaining the whole-cell configuration. A depolarizing pulse of +85 mV was applied repeatedly every 45 s from a holding potential of −70 mV. A, Mean ± se I′K-EM relations. Round arrows indicate the effect of the treatments: U73122 (long arrow) and U73343 (short arrow). Numbers of assayed cells are indicated in parentheses. B, Mean ± se I′O-EM relations of the data of A. The only arrow indicates the effect of U73122. C, Symbols show mean ± se G′K-EM relations of the data of A. Lines were calculated using Equation 2 and the averaged best-fit Boltzmann parameters (G′max, E1/2, z; shown in D) obtained from analyses of individual G′K-EMs. Arrows are as in A. D, Mean ± se best-fit Boltzmann parameters. The parameter values differ significantly if they are denoted by different letters (a, b, or c). E, Symbols show mean ± se PO-EM relationships. Lines are as in C, except for using Equation 3 here. Vertical dashed lines and arrows denote E1/2 values without (left) and with (right) U73122. Note the U73122-induced depolarizing shift of PO-EM of the K channels in the control cell.

Boltzmann analysis of the G′K-EM relationship under these treatments in steady-state conditions revealed a roughly 65% inhibition of G′max by U73122 (Fig. 10, C and D) and, notably, also a shift of the activation curve in the depolarizing (rightward) direction (Fig. 10, D and E).

DISCUSSION

NtORK Activity Is Inversely Related to Genetically Manipulated Levels of PtdInsP2 by Two Molecular Mechanisms

Two molecular mechanisms can explain the diminished NtORK activity accompanying the increased levels of PtdInsP2 in the High PIs. A major effect can be attributed to PtdInsP2 inhibition of the maximum chord conductance, G′max (which is G′K at its saturation level and, hence, voltage independent). The other can be attributed to a G′K-EM shift.

G′max

G′max is a product of the unitary conductance of a single NtORK channel, γS; of the maximum (voltage-independent) fraction of the time a channel dwells in the open state (maximum open probability [Pmax]); and of the number of NtORK channels in the plasma membrane (actually, in a unit area of it) attainable for voltage activation, N′. Thus, PtdInsP2 could decrease N′, or Pmax, or γS, or any combination of them. Which of the three factors is the more likely target for PtdInsP2 effects?

γS

In different channels, these effects seem to vary. Binding of an anionic lipid palmitoyloleoylphosphatidylglycerol to the two-transmembrane-domain bacterial K channel, KcsA, in a lipid bilayer increased γS (Marius et al., 2008). But PtdInsP2 did not seem to affect γS, neither while inhibiting the animal olfactory cyclic nucleotide-gated channels (Zhainazarov et al., 2004) nor while activating the two-transmembrane-domain KIR channels (inward-rectifying K channels; Yang et al., 2000), or the Shaker-like KCNQ channels (voltage-gated KQT-like K channels) in mammalian cells (Li et al., 2005), or the plant Shaker-like SKOR (K+-release) channel in frog oocytes (Liu et al., 2005).

Pmax

Palmitoyloleoylphosphatidylglycerol also increased the open probability of KcsA channels (Marius et al., 2008), and increased open probability was also a hallmark of PtdInsP2 activation of several other different animal channels. For example, dissociation of PtdInsP2 from the epithelial sodium channel, ENaC, decreased its open probability without affecting its plasma membrane abundance (Mace et al., 2008; for review, see Suh and Hille, 2008, and references therein). PtdInsP2 also increased the open probability of the plant SKOR channels in excised oocyte membrane patches (Liu et al., 2005). A word of caution: a change of open probability at a single membrane potential can actually mean a shift of the voltage activation curve rather than a change in the Pmax; we have not found this distinction in many of the published reports.

N′

Regulation of the activity of some ion channels, such as TRPV5 and ENaC channels in animal cells, has been shown to involve recycling between the plasma membrane and endomembranes (Lambers et al., 2007; Mace et al., 2008). For example, treatments causing the dissociation of PtdInsP2 from the ENaC subunits initiated the retrieval of ENaC protein from the plasma membrane (Mace et al., 2008). In tobacco plants, ABA treatment, known to enhance the metabolism of PtdInsP2, caused the endocytosis of the K+-influx channel, KAT1-GFP, in epidermal and guard cells within 10 to 20 min. This effect was selective, since the H+-ATPase (PMA2-GFP) in the same cells was not affected even after a 120-min exposure (Sutter et al., 2007). Endocytosis and membrane recycling have already been linked with PtdInsP2, for example in the growth of a pollen tube (Dowd et al., 2006; Helling et al., 2006). This complex link has been clarified recently in yeast. There, sites of endocytosis needed to be enriched in PtdInsP2, but for endocytosis to be completed PtdInsP2 had to be removed (Sun et al., 2007). This is consistent with enhanced turnover of PtdInsP2 being capable of promoting endocytotic internalization of ion channels. Based on this, we may expect enhanced endocytosis in the plasma membrane of the High PIs, where PtdInsP2 is metabolized at an enhanced rate (Im et al., 2007), and consequently NtORK removal from the plasma membrane is reflected in a decreased N′. Thus, we deem it most likely that a combined decrease in Pmax.N′ underlies the inhibitory effect of PtdInsP2 on NtORK G′max.

G′K-EM Shift

The other inhibitory effect of the high PtdInsP2 levels in the High PIs consists of shifting the voltage dependence of NtORK gating (the PO-EM relationship, which is the G′K-EM relationship normalized to G′max) by over 25 mV to more positive values. This means that it is more difficult to activate the channel in the High PIs, since in order to activate the same fraction of channels as in controls the High PIs require an additional depolarization of 25 mV (Fig. 3C). Such a shift has been observed also in animal cells under similar conditions of increased PtdInsP2 levels (Yaradanakul et al., 2007; for review, see Suh and Hille, 2008). The direction of this shift is consistent with the NtORK channel protein sensing an increased density of negative surface charges at the internal surface of the plasma membrane, which is consistent, in turn, with the enrichment of the internal leaflet with PtdInsP2.

The general importance of electrostatic interactions between the membrane and proteins (Mulgrew-Nesbitt et al., 2006) and, in particular, the importance of the negative surface charges of PtdInsP2 for channel activity has been highlighted elegantly (in the case of the animal KCNQ potassium channel) by increasing the cytosolic concentration of Mg2+ and applying a series of organic polycations with increasing valency. This, in quantitative agreement with neutralization of the internal negative charges, diminished channel activity (Suh and Hille, 2007; Lundbaek, 2008; see discussion by Suh and Hille, 2008). Interestingly, quantitative modeling of PtdInsP2-scavenging polycations predicted also a lack of the screening effect of polycations when PtdInsP2 concentrations in the membrane are increased (Suh and Hille, 2008). Such may be the explanation of a reported insensitivity of a plant K+-release channel to cytosolic polycations in V. faba guard cells (Liu et al., 2000). The concurrent inhibition by polycations of a K+-influx channel in these guard cells, in a whole-cell configuration but not in excised patches, was interpreted as due to a different specific mechanism rather than to PtdInsP2 charge screening (Liu et al., 2000).

In contrast to the G′K-EM shift, the sensitivity to voltage of the gating process (i.e. the slope of the PO-EM relationship, embodied in the parameter z) was not affected by PtdInsP2 levels. This is consistent with unchanged properties of the channel-gating subunits themselves.

Two Mechanisms of Enhancing NtORK Activity in High PIs by ABA Degradation of PtdInsP2

Applying ABA as a means to hydrolyze PtdInsP2 through PLC activation according to the V. faba guard cell paradigm indeed resulted in considerable lowering of the PtdInsP2 level in the High PIs (Fig. 3). Alteration of NtORK activity had the same underlying biophysical components as did genetic manipulation: lowering of the PtdInsP2 level increased maximum attainable NtORK conductance (per unit area), G′max, i.e. increased Pmax.N′.γS, or, perhaps, as suggested earlier, Pmax.N′.

Could ABA increase N′ by transcriptional activation of NtORK? It is quite unlikely, since in intact Arabidopsis suspension cells a short-term ABA treatment induced GORK mRNA, which was noticeable only after about 4 h (Becker et al., 2003). Rather, an increase of N′ could occur through removal (by PLC-mediated hydrolysis) of the PtdInsP2 from a direct inhibitory interaction with channels already in the membrane, or by recruitment of channels to the membrane through tipping the balance between endocytosis and exocytosis toward the latter when the PtdInsP2 levels declined.

Additionally, the ABA-induced decrease in the PtdInsP2 level led to a reversal of the voltage shift of the High PIs channel gating back to the control range, in line with the presumably diminished negative charge density at the internal plasma membrane surface. Resembling our results, in patch-clamp experiments conducted on protoplasts of V. faba guard cells, ABA not only increased the outward K+ currents but, under certain conditions, also caused a similar, hyperpolarizing shift of the activation curve of the K+-release channels (Lemtiri-Chlieh, 1996). These specific conditions were cytosolic K+ concentrations below 150 mm, which we interpret as cytosolic solutions of ionic strength low enough to not mask the negative surface charges on the inside of the plasma membrane.

In the controls, the minute ABA-induced changes in PtdInsP2 levels (even if significant in the case of the wild type) did not affect the activity of NtORK. This effective lack of modification of the already low PtdInsP2 level can be attributed to a simultaneous ABA activation of phospholipase D (PLD; Ritchie and Gilroy, 1998; Jacob et al., 1999; Hallouin et al., 2002; Zhang et al., 2004). Phosphatidic acid, released from the abundant phosphatidylcholine by PLD, is expected to activate the endogenous PtdIns(4)P 5-kinase (Jenkins et al., 1994; Jones et al., 2000; Wang, 2000, 2004; Wang et al., 2006) and thereby enhance the production of PtdInsP2. PtdInsP2 promotes the PLD activity, in turn producing more PtdInsP2 in a positive feedback (Huang, 2007). We are tempted to speculate that it is quite likely that in the control NT1 cell lines the ABA-stimulated opposing effects of the two phospholipases, PLC and PLD, are sufficiently well balanced to keep the PtdInsP2 level practically constant (as demonstrated in Fig. 3) and, consequently, the NtORK activity unchanged.

The lack of short-term effects of ABA on GORK channel activity in Arabidopsis guard cells (Wang et al., 2001) resembles our results with the control cell lines, but in Arabidopsis it could be due to technical reasons (the application of ABA after attaining a whole-cell configuration, i.e. on the background of altered cytoplasmic milieu and disrupted signaling cascade). In contrast, ABA enhanced within minutes K+-release channels (identified as GORK; Becker et al., 2003) in Arabidopsis suspension cells (Jeannette et al., 1999). In this case, the cells were assayed with an impaling electrode, which presumably minimized the perturbation of the internal milieu. These results resemble our own results with the High PIs, and it would be interesting to assay the effect of ABA on the PI levels in the membranes of the Arabidopsis suspension cells.

Two Mechanisms of Enhancing NtORK Activity in High PIs by Degradation of PtdInsP2 through the Removal of External Protons

In the experiments presented here, in which protoplasts were incubated at pH 7 for several minutes prior to attaining whole-cell configuration (i.e. before introducing the strongly pH-buffered patch-pipette solution to the cytosolic milieu), it is very reasonable to assume that external alkalinization of an intact protoplast led immediately to a partial, even if only transient, cytosolic alkalinization (Heppner et al., 2002; Boron, 2004). Thus, the effects of external alkalinization on NtORK could be mediated by cytosolic alkalinization.

In patch-clamp experiments on excised guard cell plasma membrane patches, cytosolic alkalinization turned out to increase the number of K+-release channels available for activation. Moreover, this process was membrane delimited (i.e. independent of soluble cytosolic components, and, in particular, independent of cytosolic [Ca2+], at least at 50 nm and 1 μm; Miedema and Assmann, 1996). This seems to suggest direct pH sensing located on the interior of the membrane. Alternatively, intracellular alkalinization, which is likely to deprotonate Ca2+-binding sites, could increase their availability for Ca2+ binding, activating PLC even at a Ca2+ concentration as low as 50 nm (Hunt et al., 2004).

Interestingly, external alkalinization enhanced the activity of TRPV5 channels in animal cells, with patch-clamp experiments excluding pH effects through the cell interior. Excluding also a direct effect on the channel protein, these experiments suggested the mediation of an external pH sensor other than the channel itself (Lambers et al., 2007).

Why were control NT1 cells unaffected by the higher pH? The minute changes in the originally low levels of membrane PtdInsP2 in the controls could be due to a balance in the activities of PLD and PLC in these cells, as argued earlier for ABA stimulation. Consequently, this could result in unchanged NtORK activity. Future experiments should address this hypothesis.

Two Mechanisms of Inhibiting NtORK Activity in High PIs and Controls by Accumulation of PtdInsP2 through PLC Inhibition

Targeting the PLC for inhibition by U73122 was expected to shift the dynamic balance between PtdInsP2 production and its cleavage (Staxen et al., 1999; Perera et al., 2001; De Jong et al., 2004; Parre et al., 2007) in both the High PIs and the control cells, wild type and C5, leading to PtdInsP2 accumulation and, consequently, to NtORK inhibition. Indeed, the inhibition of NtORK by U73122 included two elements, resembling the effect of the genetically elevated PtdInsP2 levels: depression of G′max (likely via decreasing Pmax.N′) and a shift of the voltage activation range to depolarizing potentials, consistent with PtdInsP2 accumulation in the internal leaflet of the membrane.

Physiological Significance

Taken together, our data strongly suggest that PtdInsP2 inhibits NtORK. PtdInsP2 also inhibited an anion channel in guard cells of Arabidopsis and V. faba (Lee et al., 2007). While preventing stomatal closure can be achieved, in principle, by inhibiting only one of these two ion-releasing channels, no osmotically significant loss of ions (K+ and Cl−) or stomatal closure would occur without both channels operating simultaneously. We propose that lowering of PtdInsP2 levels in guard cell plasma membrane is what activates both channels or, at least, predisposes them for activation, eventually leading to stomatal closure. The physiological initiating signal may be ABA. This type of signaling may mediate ABA-induced stomatal closure even in the absence of an observable rise in the concentration of cytosolic Ca2+ (Levchenko et al., 2005; Marten et al., 2007). PtdInsP2 hydrolysis might not elevate cytosolic Ca2+, for example, if the resulting InsP3 fails to convert to InsP6, a proposed physiological agent of Ca2+ rise in guard cells (Lemtiri-Chlieh et al., 2000, 2003). Lowering of PtdInsP2 levels may also be the underlying mechanism of the induction of stomatal closure by intracellular or extracellular alkalinization. Notably, transgenic Arabidopsis plants with lowered PtdInsP2 and InsP3 (expressing the same gene of human 5-phosphatase as in the tobacco I2-8 and I4-2 Low PIs) were more resistant to drought, losing less water through their leaves and exhibiting more efficient stomata closure (Perera et al., 2008), as would be expected from the hypothesized relief of PtdInsP2 inhibition of the ion-release channels in their guard cells.

Inverse or Direct

Interestingly, a reversible rundown of channel activity in the absence of cytosolic components required for membrane-delimited phosphorylation, hydrolyzable ATP and Mg2+, was documented for the SKOR-related K+-release channel of S. saman (presumed to be SPORK; Moran, 1996). This resembles the rundown of SKOR activity in the oocytes (Liu et al., 2005). Such rundown has been highlighted as symptomatic of a PtdInsP2 requirement for channel activity (Suh and Hille, 2008). If, indeed, SPORK requires elevated PtdInsP2 for its activity, the current models of motor cell signaling in moving leaves (Kim et al., 1996; Moran, 2007a, 2007b) will have to be altered. We posit that NtORK behavior represents the physiological relationship between K+ release channel activity and PtdInsP2 in all plant motor cells.

The fact that the PtdInsP2 level in the High PIs was elevated constitutively could not be the reason for depressed NtORK activity in these cells, since even a short-term PtdInsP2 accumulation caused by U73122 had the same inhibitory effect on the channel. The different responses of SKOR (Liu et al., 2005) and NtORK to increased PtdInsP2 level (activation versus inhibition, respectively) may be due, at least partially, to the following reasons: (1) heterologous versus homologous expression of the channels: different interactions with the surrounding milieu (types of membrane lipids, enzymes, cystoskeleton, other proteins) or different protein modifications of the channels themselves; (2) different mode of lipid application: exogenous versus in vivo; (3) different channel sequences: in spite of close homology, there could be differences, in particular at the termini and the cytosolic loops, dictating different three-dimensional structures, leading to different interactions with PtdInsP2 or with an intervening protein (Suh and Hille, 2008).

The last possibility seems the most likely. For example, SKOR, the Arabidopsis xylem-loading channel (Gaymard et al., 1998), may indeed be stimulated by elevating PtdInsP2 even in planta. Thus, a K+-release channel of maize (Zea mays) root stele, and therefore, a likely SKOR ortholog, was inhibited by pretreating the plants with ABA (Roberts, 1998), as was K+ xylem loading in barley (Hordeum vulgare; Cram and Pitman, 1972). This was quite opposite from the stimulating effect of ABA on the (unresolved) K+-release channels in V. faba guard cells (Lemtiri-Chlieh and MacRobbie, 1994; Lemtiri-Chlieh, 1996) or on GORK in Arabidopsis suspension cells (Jeannette et al., 1999).

Is NtORK like SKOR or like GORK? Based on comparison of the amino acid sequences, NtORK1 (the sole gene of the K+-release channel in the tobacco suspension cells; Sano et al., 2008) is more similar to SKOR than to GORK (72% versus 66% identical; Sano et al., 2008). However, because NtORK1's dominant distribution in tobacco plant leaves (Sano et al., 2008) resembles that of GORK in Arabidopsis (Becker et al., 2003), NtORK is likely a GORK ortholog (Sano et al., 2008). Our present results support this view.

CONCLUSION

The previously observed correlations between the phospholipid level and GORK (and, very likely, SPORK) activity in plant motor cells were extended here into a causal relationship between the PtdInsP2 level and the activity of a homologous channel, NtORK. This was achieved by manipulating the endogenous levels of PtdInsP2 in the plant cell membrane, on a long- or a short-term scale, while monitoring the in situ NtORK activity, as prescribed by a recent critical review: “The more ways you can change the PIP2 [PtdInsP2], the stronger the evidence becomes” (Suh and Hille, 2008). Our findings are consistent with NtORK inhibition by the negatively charged PtdInsP2 in the internal plasma membrane leaflet. Biophysical analysis of NtORK whole-cell outward K+ currents provided an insight into a possible mechanism underlying this causality. Thus, NtORK activity was diminished mainly through decreased maximum available conductance via the channels (Gmax), and, to a somewhat lesser extent, by altering the voltage dependence of channel activation and making the channels more difficult to open. Such effects are likely to underlie PI signaling in intact plant cells.

We are aware that our observations are only the beginning of a prolonged exploration of the possible interactions of PIs with plant ion channels and with other proteins (Suh and Hille, 2008). Although PIs are much less abundant in the plant plasma membrane than in the animal plasma membrane, the wealth of reports on plant PI signaling suggests that channel-PtdInsP2 interactions in the plant cell will not be much rarer. Because ion channels are crucial for signaling and osmotic homeostasis, understanding these interactions will provide a handle for manipulating plant water relations.

MATERIALS AND METHODS

Plant Material

Cell Lines

One wild-type and eight transgenic lines of tobacco (Nicotiana tabacum) cultured cells, NT1, were used in this work: two High PIs, cell lines expressing the GFP-fused human phosphatidylinositol (4)phosphate 5-kinase, type Iα, HsPIPKIα-2 and HsPIPKIα-3, and a control GFP line, transformed with the same vector but with GFP alone (Im et al., 2007); two Low PIs, cell lines expressing the human-type InsP 5-phosphatase, I2-8 (Perera et al., 2002) and I4-2, both with membrane-associated phosphatase; three controls for the Low PIs: C-5, an empty vector control, C348S, an inactive mutant phosphatase, and ΔC, a truncated soluble phosphatase localized in the cytosol. The soluble form of the InsP 5- phosphatase ΔC lacks the C-terminal isoprenylation site (the last four amino acids; De Smedt et al., 1997). The inactive mutant C348S has a single amino acid substitution (Cys-348 to Ser) in the catalytic domain (Communi and Erneux, 1996). The three InsP 5-phosphatase constructs (I4-2, C348S, and ΔC) were subcloned into the Gateway binary vector pK2GW7 containing a cauliflower mosaic virus 35S promoter (Functional Genomics Division, Department of Plant Systems Biology, University of Gent, Belgium), and the DNA sequence was verified by sequencing. Tobacco cell transformation and selection of transgenic tobacco lines were as described previously (Perera et al., 2002).

Tissue Culture

Tobacco (‘Bright Yellow 2’) cultured cells (NT1) were maintained in 16 mL of liquid culture medium (see “Solutions” below). The 100-mL Erlenmeyer flasks with cells were agitated at about 125 rpm in the dark at about 28°C. Cells were subcultured every 7 d at a 1:16 (v/v) dilution with fresh medium at room temperature (Perera et al., 2002).

Protoplast Isolation

Protoplasts were isolated from the tobacco cells at 4 d (4 × 24 h) after subculture. A 0.5-mL suspension was centrifuged at 36g for 5 min, and the upper medium was poured off and quickly replaced with 2.5 mL of cell wall digestion solution (see “Solutions” below). Subsequently, the cells were agitated on a rotary shaker at about 60 rpm for 1.5 h at 30°C. The enzymatic reaction was stopped by washing the cells with 5 mL of isotonic solution (see below) through a nylon filter (50-μm mesh) into a 12- to 15-mL test tube. The test tube was centrifuged at 36g for 5 min. The supernatant was discarded, and the protoplasts were resuspended in 300 μL of isotonic solution in the same test tube. The isolation procedure was conducted at room temperature. To prevent regrowth of cell walls and reproduction of bacteria, the protoplasts were placed on ice for the duration of the experiment (up to 9 h).

Patch-Clamp Experiments

Procedure

Patch-clamp experiments were performed at room temperature (20°C–22°C) using a Digidata 3122A interface and the pClamp 9 or 10 program suite from Axon Instruments, which was used both for running the experiment and analysis. Fire-polished borosilicate glass patch-clamp pipettes (Sutter Instruments; catalog no. BF150-86-10) had resistance of 50 to 100 MΩ in the external solution (see “Solutions” below). A drop with protoplasts was added to the external solution in the bath, and the protoplasts were allowed to settle for several minutes or the bath was filled with the external solution after the drop with protoplasts was placed on the chamber bottom (the order did not influence the results). Whole-cell configuration was attained usually spontaneously without obtaining a giga-seal. Recording started several minutes after decrease and stabilization of the baseline current at the holding potential of −70 mV, usually within about 10 min. Outward K+ currents were recorded from the protoplasts applying 1- to 3-s-long voltage pulses between +85 and −110 mV in −15-mV voltage steps at 45-s intervals. All experiments were performed in voltage-clamp mode. The error in the voltage clamping of the whole-cell membrane, largely due to the series resistance of the patch pipette, was compensated at approximately 80% by analog circuitry of the amplifier. Mean series resistance was 15.8 ± 5.4 MΩ (±sd, n = 106). Currents were filtered at 500 Hz and sampled usually at 1 to 2 kHz.

Analysis

Prior to averaging, a normalized net steady-state current, I′K, was obtained by subtracting the instantaneous current from the total steady-state current, then dividing by the cell's capacitance, as read off the amplifier dial. The normalized instantaneous current, I′O, was obtained similarly. Mean capacitance was 32.9 ± 9.4 pF (n = 106). The mean diameter of protoplasts selected for these experiments was 45.4 ± 6.3 μm (n = 106). The average specific capacitance was 0.51 ± 0.10 μF cm−2 (n = 106).

The normalized chord conductance, G′K, was extracted from I′K according to Equation 1:Math(1)where EM is the membrane potential and Erev is the current reversal potential, determined separately for each cell line (as described in Supplemental Fig. S2). Individual G′K-EM relationships were fitted with the Boltzmann equation (Hille, 2001) using Origin (version 7.0220; Origin Lab Co.), according to Equation 2:Math(2)where G′max is the maximum conductance (normalized to capacitance), E1/2 is the voltage at which half of G′max is attained, and z is the effective charge of the gating subunits. The individual best-fit parameter values (G′max, E1/2, and z) were then averaged for each cell line.

Channel open probability, PO, was obtained by normalizing G′K to G′max, according to Equation 3:Math(3)

Other details were as published previously (Yu et al., 2001). Differences between means were deemed significant if, using a two-sided Student's t test, P < 0.05.

Solutions

Bath solution included (in mM): 5 KCl, 1 CaCl2, and 10 MES. pH was 5.6, and osmolarity was 435 mOsm. Pipette solution included (in mM): 150 KCl, 20 HEPES, 5 MgCl2, 2 K4-1,2-bis(o-aminophenoxy) ethane-N,N,N,N-tetraacetic acid (BAPTA), and 2 K2ATP. pH was 7.5, and osmolarity was 470 mOsm. pH in both solutions was adjusted by N-methyl d-glucamine base and osmolarity by d-sorbitol. Pipette solution was filtered before use.

Culture solution was 4.3 g L−1 Murashige and Skoog solution (Sigma; catalog no. M-5524) supplemented with 2 g L−1 KH2PO4, 1 g L−1 myoinositol, 30 g L−1 Suc, 100 μL L−1 thiamine-HCl, and 4 μL L−1 2,4-dichlorophenoxyacetic acid. pH was adjusted to 5.8 with KOH, and the solution was autoclaved for 20 min.

ABA (Sigma; catalog no. 862169) 10 mm stock solution was prepared by dissolving 13 mg of powder in approximately 100 μL of 1 m KOH and completing the volume with bath solution to 5 mL. After adjusting pH to 5.6 by MES, the stock solution was stored at −20°C.

U73122 (Calbiochem; catalog no. 662035) and U73343 (Calbiochem; catalog no. 662041) 5 mm stock solutions were prepared in dimethyl sulfoxide (Fluka; catalog no. 41650).

K4-BAPTA was from Molecular Probes, and other chemicals were from Sigma or Merck and were of analytical grade.

Determination of PI Levels

PtdIns(4,5)P2 Mass Measurements

Protoplasts were harvested by centrifugation, plasma membranes were isolated by aqueous two-phase partitioning, lipids were extracted, and PtdIns(4,5)P2 mass measurements were carried out as described (Heilmann et al., 2001).

InsP3 Determination

Either the membrane lipid hydrolysate (as above) was assayed, or, to measure total InsP3 level, cells were harvested by filtration and immediately frozen in liquid N2, ground to a fine powder, and precipitated with cold 10% (v/v) perchloric acid. InsP3 assays were carried out using the TRK1000 InsP3 assay kit (GE Healthcare Life Sciences) as described previously (Perera et al., 1999, 2002).

Supplemental Data

The following materials are available in the online version of this article.

  • Supplemental Figure S1. Identification of K channel currents using K channel blockers.

  • Supplemental Figure S2. Determination of the reversal potential, Erev.

  • Supplemental Figure S3. The effect of PtdInsP2 on whole-cell currents.

  • Supplemental Figure S4. Subcellular localization of the 5-phosphatase in the Low PIs.

  • Supplemental Figure S5. InsP3 content in the InsP 5-phosphatase-harboring transgenic cells and their controls.

Acknowledgments

We thank Dr. O. Shaul and Ms. D. Dolev for advice on NT1/BY2 cultures and Prof. A. Moran for critical reading of the manuscript.

Footnotes

  • The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Wendy F. Boss (wendy_boss{at}ncsu.edu).

  • www.plantphysiol.org/cgi/doi/10.1104/pp.108.129007

  • ↵1 This work was supported by the United States-Israel Binational Science Foundation (grant no. 2000191 to N.M. and W.F.B.), the Israel Science Foundation (grant no. 550/01 to N.M.), the U.S. National Science Foundation (grant no. MCB–0718452 to W.F.B. and I.P.), and the U.S. Department of Agriculture-Cooperative State Research, Education, and Extension Service (grant no. 2004–35100–14892 to I.P.).

  • ↵2 Present address: Department of Psychiatry and Psychotherapy, Institute of Neurophysiology, Charité Medical University, Berlin 10117, Germany.

  • ↵3 Present address: Department of Physiology, Emory University School of Medicine, Atlanta, GA 30322.

  • ↵4 Present address: Department of Genetics, University of Wisconsin, Madison, WI 53706–1580.

  • ↵[OA] Open Access articles can be viewed online without a subscription.

  • ↵[W] The online version of this article contains Web-only data.

  • Received September 1, 2008.
  • Accepted November 24, 2008.
  • Published December 3, 2008.

LITERATURE CITED

  1. ↵
    Becker D, Hoth S, Ache P, Wenkel S, Roelfsema MRG, Meyerhoff O, Hartung W, Hedrich R (2003) Regulation of the ABA-sensitive Arabidopsis potassium channel gene GORK in response to water stress. FEBS Lett 554: 119–126
    OpenUrlCrossRefPubMed
  2. ↵
    Berridge MJ, Bootman MD, Lipp P (1998) Calcium: a life and death signal. Nature 395: 645–648
    OpenUrlCrossRefPubMed
  3. ↵
    Berridge MJ, Irvine RF (1984) Inositol trisphosphate, a novel second messenger in cellular signal transduction. Nature 312: 315–321
    OpenUrlCrossRefPubMed
  4. ↵
    Blatt MR (1990) Potassium channel currents in intact stomatal guard cells: rapid enhancement by abscisic acid. Planta 180: 445–455
    OpenUrlCrossRefPubMed
  5. ↵
    Blatt MR (2000) Cellular signaling and volume control in stomatal movements in plants. Annu Rev Cell Dev Biol 16: 221–241
    OpenUrlCrossRefPubMed
  6. ↵
    Blatt MR, Armstrong F (1993) K+ channels of stomatal guard cells: abscisic-acid-evoked control of the outward rectifier mediated by cytoplasmic pH. Planta 191: 330–341
    OpenUrlCrossRef
  7. ↵
    Blatt MR, Thiel G, Trentham DR (1990) Reversible inactivation of K+ channels of Vicia stomatal guard cells following the photolysis of caged inositol 1,4,5-trisphosphate. Nature 346: 766–769
    OpenUrlCrossRefPubMed
  8. ↵
    Bleasdale JE, Thakur NR, Gremban RS, Bundy GL, Fitzpatrick FA, Smith RJ, Bunting S (1990) Selective inhibition of receptor-coupled phospholipase C-dependent processes in human platelets and polymorphonuclear neutrophils. J Pharmacol Exp Ther 255: 756–768
    OpenUrlAbstract/FREE Full Text
  9. ↵
    Boron WF (2004) Regulation of intracellular pH. Adv Physiol Educ 28: 160–179
    OpenUrlAbstract/FREE Full Text
  10. ↵
    Communi D, Erneux C (1996) Identification of an active site cysteine residue in human type I Ins(1,4,5)P3 5-phosphatase by chemical modification and site-directed mutagenesis. Biochem J 320: 181–186
    OpenUrlAbstract/FREE Full Text
  11. ↵
    Cram WJ, Pitman MG (1972) Action of abscisic acid on ion uptake and water flow in plant roots. Aust J Biol Sci 25: 1125–1132
    OpenUrl
  12. ↵
    De Jong CF, Laxalt AM, Bargmann BOR, de Wit P, Joosten M, Munnik T (2004) Phosphatidic acid accumulation is an early response in the Cf-4/Avr4 interaction. Plant J 39: 1–12
    OpenUrlCrossRefPubMed
  13. ↵
    De Smedt F, Missiaen L, Parys JB, Vanweyenberg V, De Smedt H, Erneux C (1997) Isoprenylated human brain type I inositol 1,4,5-trisphosphate 5-phosphatase controls Ca2+ oscillations induced by ATP in Chinese hamster ovary cells. J Biol Chem 272: 17367–17375
    OpenUrlAbstract/FREE Full Text
  14. ↵
    Dowd PE, Coursol S, Skirpan AL, Kao T, Gilroy S (2006) Petunia phospholipase C1 is involved in pollen tube growth. Plant Cell 18: 1438–1453
    OpenUrlAbstract/FREE Full Text
  15. ↵
    Gaymard F, Lacombe B, Bouchez D, Bruneau D, Boucherez J, Michaux-Ferriere N, Thibaud JB, Sentenac H (1998) Identification and disruption of a plant Shaker-like outward channel involved in K+ release into the xylem sap. Cell 94: 647–655
    OpenUrlCrossRefPubMed
  16. ↵
    Hallouin M, Ghelis T, Brault M, Bardat F, Cornel D, Miginiac E, Rona JP, Sotta B, Jeannette E (2002) Plasmalemma abscisic acid perception leads to RAB18 expression via phospholipase D activation in Arabidopsis suspension cells. Plant Physiol 130: 265–272
    OpenUrlAbstract/FREE Full Text
  17. ↵
    Hedrich R, Neimanis S, Savchenko G, Felle HH, Kaiser WM, Heber U (2001) Changes in apoplastic pH and membrane potential in leaves in relation to stomatal responses to CO2, malate, abscisic acid or interruption of water supply. Planta 213: 594–601
    OpenUrlCrossRefPubMed
  18. ↵
    Heilmann I, Perera IY, Gross W, Boss WF (2001) Plasma membrane phosphatidylinositol 4,5-bisphosphate levels decrease with time in culture. Plant Physiol 126: 1507–1518
    OpenUrlAbstract/FREE Full Text
  19. ↵
    Helling D, Possart A, Cottier S, Klahre U, Kost B (2006) Pollen tube tip growth depends on plasma membrane polarization mediated by tobacco PLC3 activity and endocytic membrane recycling. Plant Cell 18: 3519–3534
    OpenUrlAbstract/FREE Full Text
  20. ↵
    Heppner TJ, Bonev AD, Santana LF, Nelson MT (2002) Alkaline pH shifts Ca2+ sparks to Ca2+ waves in smooth muscle cells of pressurized cerebral arteries. Am J Physiol Heart Circ Physiol 283: H2169–H2176
    OpenUrlAbstract/FREE Full Text
  21. ↵
    Hetherington AM (2001) Guard cell signaling. Cell 107: 711–714
    OpenUrlCrossRefPubMed
  22. ↵
    Hilgemann DW (2003) Getting ready for the decade of the lipids. Annu Rev Physiol 65: 697–700
    OpenUrlCrossRefPubMed
  23. ↵
    Hilgemann DW (2004) Biochemistry: oily barbarians breach ion channel gates. Science 304: 223–224
    OpenUrlAbstract/FREE Full Text
  24. ↵
    Hille B (2001) Ionic Channels of Excitable Membranes, Ed 3. Sinauer Associates, Sunderland, MA, pp 56–59
  25. ↵
    Hosoi S, Lino M, Shimazaki KI (1988) Outward-rectifying K+ channels in stomatal guard cell protoplasts. Plant Cell Physiol 29: 907–911
    OpenUrlAbstract/FREE Full Text
  26. ↵
    Huang CL (2007) Complex roles of PIP2 in the regulation of ion channels and transporters. Am J Physiol Renal Physiol 293: F1761–F1765
    OpenUrlAbstract/FREE Full Text
  27. ↵
    Hunt L, Otterhag L, Lee JC, Lasheen T, Hunt J, Seki M, Shinozaki K, Sommarin M, Gilmour DJ, Pical C, et al (2004) Gene-specific expression and calcium activation of Arabidopsis thaliana phospholipase C isoforms. New Phytol 162: 643–654
    OpenUrlCrossRef
  28. ↵
    Im YJ, Perera IY, Brglez I, Johannes E, Allen NS, Boss WF (2007) Plant cells with a 100-fold increase in plasma membrane phosphatidylinositol(4,5)bisphosphate identify a flux-limiting enzyme. Plant Cell 19: 1603–1616
    OpenUrlAbstract/FREE Full Text
  29. ↵
    Irving HR, Gehring CA, Parish RW (1992) Changes in cytosolic pH and calcium of guard cells precede stomatal movements. Proc Natl Acad Sci USA 89: 1970–1994
    OpenUrl
  30. ↵
    Jacob T, Ritchie S, Assmann SM, Gilroy S (1999) Abscisic acid signal transduction in guard cells is mediated by phospholipase D activity. Proc Natl Acad Sci USA 96: 12192–12197
    OpenUrlAbstract/FREE Full Text
  31. ↵
    Jeannette E, Rona JP, Bardat F, Cornel D, Sotta B, Miginiac E (1999) Induction of RAB18 gene expression and activation of K+ outward rectifying channels depend on an extracellular perception of ABA in Arabidopsis thaliana suspension cells. Plant J 18: 13–22
    OpenUrlCrossRefPubMed
  32. ↵
    Jenkins GH, Fisette PL, Anderson RA (1994) Type I phosphatidylinositol 4-phosphate 5-kinase isoforms are specifically stimulated by phosphatidic acid. J Biol Chem 269: 11547–11554
    OpenUrlAbstract/FREE Full Text
  33. ↵
    Jones DR, Sanjuan MA, Merida I (2000) Type Iα phosphatidylinositol 4-phosphate 5-kinase is a putative target for increased intracellular phosphatidic acid. FEBS Lett 476: 160–165
    OpenUrlCrossRefPubMed
  34. ↵
    Kasukabe N, Watanabe-Sugimoto M, Matsuoka K, Okuma E, Obi I, Nakamura Y, Shimoishi Y, Murata Y, Kakutani T (2006) Expression and Ca2+ dependency of plasma membrane K+ channels of tobacco suspension cells adapted to salt stress. Plant Cell Physiol 47: 1674–1677
    OpenUrlAbstract/FREE Full Text
  35. ↵
    Kim HY, Cote GG, Crain RC (1996) Inositol 1,4,5-trisphosphate may mediate closure of K+ channels by light and darkness in Samanea saman motor cells. Planta 198: 279–287
    OpenUrlPubMed
  36. ↵
    Lambers TT, Oancea E, de Groot T, Topala CN, Hoenderop JG, Bindels RJ (2007) Extracellular pH dynamically controls cell surface delivery of functional TRPV5 channels. Mol Cell Biol 27: 1486–1494
    OpenUrlAbstract/FREE Full Text
  37. ↵
    Langer K, Ache P, Geiger D, Stinzing A, Arend M, Wind C, Regan S, Fromm J, Hedrich R (2002) Poplar potassium transporters capable of controlling K+ homeostasis and K+-dependent xylogenesis. Plant J 32: 997–1009
    OpenUrlCrossRefPubMed
  38. ↵
    Lee Y, Kim YW, Jeon BW, Park KY, Suh SJ, Seo J, Kwak JM, Martinoia E, Hwang I, Lee Y (2007) Phosphatidylinositol 4,5-bisphosphate is important for stomatal opening. Plant J 52: 803–816
    OpenUrlCrossRefPubMed
  39. ↵
    Lee YS, Choi YB, Suh S, Lee J, Assmann SM, Joe CO, Kelleher JF, Crain RC (1996) Abscisic acid-induced phosphoinositide turnover in guard cell protoplasts of Vicia faba. Plant Physiol 110: 987–996
    OpenUrlAbstract
  40. ↵
    Lemtiri-Chlieh F (1996) Effects of internal K+ and ABA on the voltage- and time-dependence of the outward K+-rectifier in Vicia guard cells. J Membr Biol 153: 105–116
    OpenUrlCrossRefPubMed
  41. ↵
    Lemtiri-Chlieh F, MacRobbie EA (1994) Role of calcium in the modulation of Vicia guard cell potassium channels by abscisic acid: a patch-clamp study. J Membr Biol 137: 99–107
    OpenUrlPubMed
  42. ↵
    Lemtiri-Chlieh F, MacRobbie EAC, Brearley CA (2000) Inositol hexakisphosphate is a physiological signal regulating the K+-inward-rectifying conductance in guard cells. Proc Natl Acad Sci USA 97: 8687–8692
    OpenUrlAbstract/FREE Full Text
  43. ↵
    Lemtiri-Chlieh F, MacRobbie EAC, Webb AAR, Manison NF, Brownlee C, Skepper JN, Chen J, Prestwich GD, Brearley CA (2003) Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cells. Proc Natl Acad Sci USA 100: 10091–10095
    OpenUrlAbstract/FREE Full Text
  44. ↵
    Levchenko V, Konrad KR, Dietrich P, Roelfsema MR, Hedrich R (2005) Cytosolic abscisic acid activates guard cell anion channels without preceding Ca2+ signals. Proc Natl Acad Sci USA 102: 4203–4208
    OpenUrlAbstract/FREE Full Text
  45. ↵
    Li Y, Gamper N, Hilgemann DW, Shapiro MS (2005) Regulation of Kv7 (KCNQ) K+ channel open probability by phosphatidylinositol 4,5-bisphosphate. J Neurosci 25: 9825–9835
    OpenUrlAbstract/FREE Full Text
  46. ↵
    Liu K, Fu HH, Bei QX, Luan S (2000) Inward potassium channel in guard cells as a target for polyamine regulation of stomatal movements. Plant Physiol 124: 1315–1325
    OpenUrlAbstract/FREE Full Text
  47. ↵
    Liu K, Li LG, Luan S (2005) An essential function of phosphatidylinositol phosphates in activation of plant shaker-type K+ channels. Plant J 42: 433–443
    OpenUrlCrossRefPubMed
  48. ↵
    Lundbaek JA (2008) Lipid bilayer-mediated regulation of ion channel function by amphiphilic drugs. J Gen Physiol 131: 421–429
    OpenUrlFREE Full Text
  49. ↵
    Mace OJ, Woollhead AM, Baines DL (2008) AICAR activates AMPK and alters PIP2 association with ENaC to inhibit Na+ transport in H441 lung epithelial cells. J Physiol 586: 4541–4557
    OpenUrlCrossRefPubMed
  50. ↵
    Macrobbie EAC (1992) Calcium and ABA-induced stomatal closure. Philos Trans R Soc Ser B Biol Sci 338: 5–18
    OpenUrlAbstract/FREE Full Text
  51. ↵
    Marius P, Zagnoni M, Sandison ME, East JM, Morgan H, Lee AG (2008) Binding of anionic lipids to at least three nonannular sites on the potassium channel KcsA is required for channel opening. Biophys J 94: 1689–1698
    OpenUrlCrossRefPubMed
  52. ↵
    Marten H, Konrad KR, Dietrich P, Roelfsema MRG, Hedrich R (2007) Ca2+-dependent and -independent abscisic acid activation of plasma membrane anion channels in guard cells of Nicotiana tabacum. Plant Physiol 143: 28–37
    OpenUrlAbstract/FREE Full Text
  53. ↵
    Mayer WE, Hohloch C, Kalkuhl A (1997) Extensor protoplasts of the Phaseolus pulvinus: light-induced swelling may require extracellular Ca2+ influx, dark-induced shrinking, inositol 1,4,5-trisphosphate-induced Ca2+ mobilization. J Exp Bot 48: 219–228
    OpenUrlAbstract/FREE Full Text
  54. ↵
    Meijer HJG, Munnik T (2003) Phospholipid-based signaling in plants. Annu Rev Plant Biol 54: 265–306
    OpenUrlCrossRefPubMed
  55. ↵
    Miedema H, Assmann SM (1996) A membrane-delimited effect of internal pH on the K+ outward rectifier of Vicia faba guard cells. J Membr Biol 154: 227–237
    OpenUrlCrossRefPubMed
  56. ↵
    Moran N (1996) Membrane-delimited phosphorylation enables the activation of the outward-rectifying K channels in a plant cell. Plant Physiol 111: 1281–1292
    OpenUrlAbstract
  57. ↵
    Moran N (2007a) Osmoregulation of leaf motor cells. FEBS Lett 581: 2337–2347
    OpenUrlCrossRefPubMed
  58. ↵
    Moran N (2007b) Rhythmic leaf movements: physiological and molecular aspects. In S Mancuso, S Shabala, eds, Rhythms in Plants: Phenomenology, Mechanisms, and Adaptive Significance. Springer-Verlag, Berlin/Heidelberg, pp 3–38
  59. ↵
    Moshelion M, Moran N (2000) K+-efflux channels in extensor and flexor cells of Samanea saman are not identical: effects of cytosolic Ca2+. Plant Physiol 124: 911–919
    OpenUrlAbstract/FREE Full Text
  60. ↵
    Mulgrew-Nesbitt A, Diraviyam K, Wang J, Singh S, Murray P, Li Z, Rogers L, Mirkovic N, Murray D (2006) The role of electrostatics in protein-membrane interactions. Biochim Biophys Acta 1761: 812–826
    OpenUrlCrossRefPubMed
  61. ↵
    Pandey S, Zhang W, Assmann SM (2007) Roles of ion channels and transporters in guard cell signal transduction. FEBS Lett 581: 2325–2336
    OpenUrlCrossRefPubMed
  62. ↵
    Parre E, Ghars MA, Leprince AS, Thiery L, Lefebvre D, Bordenave M, Richard L, Mazars C, Abdelly C, Savoure A (2007) Calcium signaling via phospholipase C is essential for proline accumulation upon ionic but not nonionic hyperosmotic stresses in Arabidopsis. Plant Physiol 144: 503–512
    OpenUrlAbstract/FREE Full Text
  63. ↵
    Perera IY, Heilmann I, Boss WF (1999) Transient and sustained increases in inositol 1,4,5-trisphosphate precede the differential growth response in gravistimulated maize pulvini. Proc Natl Acad Sci USA 96: 5838–5843
    OpenUrlAbstract/FREE Full Text
  64. ↵
    Perera IY, Heilmann I, Chang SC, Boss WF, Kaufman PB (2001) A role for inositol 1,4,5-trisphosphate in gravitropic signaling and the retention of cold-perceived gravistimulation of oat shoot pulvini. Plant Physiol 125: 1499–1507
    OpenUrlAbstract/FREE Full Text
  65. ↵
    Perera IY, Hung CY, Moore CD, Stevenson-Paulik J, Boss WF (2008) Transgenic Arabidopsis plants expressing the type 1 inositol 5-phosphatase exhibit increased drought tolerance and altered abscisic acid signaling. Plant Cell 20: 2876–2893
    OpenUrlAbstract/FREE Full Text
  66. ↵
    Perera IY, Love J, Heilmann I, Thompson WF, Boss WF (2002) Up-regulation of phosphoinositide metabolism in tobacco cells constitutively expressing the human type I inositol polyphosphate 5-phosphatase. Plant Physiol 129: 1795–1806
    OpenUrlAbstract/FREE Full Text
  67. ↵
    Ritchie S, Gilroy S (1998) Abscisic acid signal transduction in the barley aleurone is mediated by phospholipase D activity. Proc Natl Acad Sci USA 95: 2697–2702
    OpenUrlAbstract/FREE Full Text
  68. ↵
    Roberts SK (1998) Regulation of K+ channels in maize roots by water stress and abscisic acid. Plant Physiol 116: 145–153
    OpenUrlAbstract/FREE Full Text
  69. ↵
    Sano T, Becker D, Ivashikina N, Wegner LH, Zimmermann U, Roelfsema MRG, Nagata T, Hedrich R (2007) Plant cells must pass a K+ threshold to re-enter the cell cycle. Plant J 50: 401–413
    OpenUrlCrossRefPubMed
  70. ↵
    Sano T, Kutsuna N, Becker D, Hedrich R, Hasezawa S (2008) Outward-rectifying K+ channel activities regulate cell elongation and cell division of tobacco BY-2 cells. Plant J 57: 57–64
    OpenUrl
  71. ↵
    Schroeder JI, Kwak JM, Allen GJ (2001) Guard cell abscisic acid signalling and engineering drought hardiness in plants. Nature 410: 327–330
    OpenUrlCrossRefPubMed
  72. ↵
    Staxen I, Pical C, Montgomery LT, Gray JE, Hetherington AM, McAinsh MR (1999) Abscisic acid induces oscillations in guard-cell cytosolic free calcium that involve phosphoinositide-specific phospholipase C. Proc Natl Acad Sci USA 96: 1779–1784
    OpenUrlAbstract/FREE Full Text
  73. ↵
    Stoeckel H, Takeda K (2002) Plasmalemmal voltage-activated K+ currents in protoplasts from tobacco BY-2 cells: possible regulation by actin microfilaments? Protoplasma 220: 79–87
    OpenUrlCrossRefPubMed
  74. ↵
    Suh BC, Hille B (2005) Regulation of ion channels by phosphatidylinositol 4,5-bisphosphate. Curr Opin Neurobiol 15: 370–378
    OpenUrlCrossRefPubMed
  75. ↵
    Suh BC, Hille B (2007) Electrostatic interaction of internal Mg2+ with membrane PIP2 seen with KCNQ K+ channels. J Gen Physiol 130: 241–256
    OpenUrlAbstract/FREE Full Text
  76. ↵
    Suh BC, Hille B (2008) PIP2 is a necessary cofactor for ion channel function: how and why? Annu Rev Biophys 37: 175–195
    OpenUrlCrossRefPubMed
  77. ↵
    Suh S, Moran N, Lee Y (2000) Blue light activates depolarization-dependent K+ channels in flexor cells from Samanea saman motor organs via two mechanisms. Plant Physiol 123: 833–843
    OpenUrlAbstract/FREE Full Text
  78. ↵
    Sun Y, Carroll S, Kaksonen M, Toshima JY, Drubin DG (2007) PtdIns(4,5)P2 turnover is required for multiple stages during clathrin- and actin-dependent endocytic internalization. J Cell Biol 177: 355–367
    OpenUrlAbstract/FREE Full Text
  79. ↵
    Sutter JU, Sieben C, Hartel A, Eisenach C, Thiel G, Blatt MR (2007) Abscisic acid triggers the endocytosis of the Arabidopsis KAT1 K+ channel and its recycling to the plasma membrane. Curr Biol 17: 1396–1402
    OpenUrlCrossRefPubMed
  80. ↵
    Wang X (2000) Multiple forms of phospholipase D in plants: the gene family, catalytic and regulatory properties, and cellular functions. Prog Lipid Res 39: 109
    OpenUrlCrossRefPubMed
  81. ↵
    Wang X, Devaiah SP, Zhang W, Welti R (2006) Signaling functions of phosphatidic acid. Prog Lipid Res 45: 250
    OpenUrlCrossRefPubMed
  82. ↵
    Wang XM (2004) Lipid signaling. Curr Opin Plant Biol 7: 329–336
    OpenUrlCrossRefPubMed
  83. ↵
    Wang XQ, Ullah H, Jones AM, Assmann SM (2001) G protein regulation of ion channels and abscisic acid signaling in Arabidopsis guard cells. Science 292: 2070–2072
    OpenUrlAbstract/FREE Full Text
  84. ↵
    Yang Z, Xu H, Cui N, Qu Z, Chanchevalap S, Shen W, Jiang C (2000) Biophysical and molecular mechanisms underlying the modulation of heteromeric Kir4.1-Kir5.1 channels by CO2 and pH. J Gen Physiol 116: 33–46
    OpenUrlAbstract/FREE Full Text
  85. ↵
    Yaradanakul A, Feng S, Shen C, Lariccia V, Lin MJ, Yang J, Kang TM, Dong P, Yin HL, Albanesi JP, et al (2007) Dual control of cardiac Na+ Ca2+ exchange by PIP2: electrophysiological analysis of direct and indirect mechanisms. J Physiol 582: 991–1010
    OpenUrlCrossRefPubMed
  86. ↵
    Yu L, Moshelion M, Moran N (2001) Extracellular protons inhibit the activity of inward-rectifying K channels in the motor cells of Samanea saman pulvini. Plant Physiol 127: 1310–1322
    OpenUrlAbstract/FREE Full Text
  87. ↵
    Zhainazarov AB, Spehr M, Wetzel CH, Hatt H, Ache BW (2004) Modulation of the olfactory CNG channel by Ptdlns(3,4,5)P3. J Membr Biol 201: 51–57
    OpenUrlCrossRefPubMed
  88. ↵
    Zhang WH, Qin CB, Zhao J, Wang XM (2004) Phospholipase D alpha 1-derived phosphatidic acid interacts with ABI1 phosphatase 2C and regulates abscisic acid signaling. Proc Natl Acad Sci USA 101: 9508–9513
    OpenUrlAbstract/FREE Full Text
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Phosphatidylinositol (4,5)Bisphosphate Inhibits K+-Efflux Channel Activity in NT1 Tobacco Cultured Cells
Xiaohong Ma, Oded Shor, Sofia Diminshtein, Ling Yu, Yang Ju Im, Imara Perera, Aaron Lomax, Wendy F. Boss, Nava Moran
Plant Physiology Feb 2009, 149 (2) 1127-1140; DOI: 10.1104/pp.108.129007
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