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The Journal of Neuroscience, January 15, 1998, 18(2):679-686

Angiotensin II Type 2 Receptor Stimulation of Neuronal Delayed-Rectifier Potassium Current Involves Phospholipase A₂ and Arachidonic Acid

Mingyan Zhu, Craig H. Gelband, Jennifer M. Moore, Philip Posner, and Colin Sumners

Department of Physiology, University of Florida, College of Medicine, Gainesville, Florida 32610

	ABSTRACT

Top Abstract Introduction Materials & Methods Results Discussion References

Angiotensin II (Ang II) elicits an Ang II type 2 (AT₂) receptor-mediated increase in delayed-rectifier K⁺ current (I_K) in neurons cultured from newborn rat hypothalamus and brainstem. This effect involves a pertussis toxin (PTX)-sensitive G_i protein and is abolished by inhibition of serine and threonine phosphatase 2A (PP-2A). Here, we determined that Ang II stimulates [³H]arachidonic acid (AA) release from cultured neurons via AT₂ receptors. This effect of Ang II was blocked by inhibition of phospholipase A₂ (PLA₂) and by PTX. Because AA and its metabolites are powerful modulators of neuronal K⁺ currents, we investigated the involvement of PLA₂ and AA in the AT₂ receptor-mediated stimulation of I_K by Ang II. Single-cell reverse transcriptase (RT)-PCR analyses revealed the presence of PLA₂ mRNA in neurons that responded to Ang II with an increase in I_K. The stimulation of neuronal I_K by Ang II was attenuated by selective inhibitors of PLA₂ and was mimicked by application of AA to neurons. Inhibition of lipoxygenase (LO) enzymes significantly reduced both Ang II- and AA-stimulated I_K, and the 12-LO metabolite of AA 12S-hydroxyeicosatetraenoic acid (12S-HETE) stimulated I_K. These data indicate the involvement of a PLA₂, AA, and LO metabolite intracellular pathway in the AT₂ receptor-mediated stimulation of neuronal I_K by Ang II. Furthermore, the demonstration that inhibition of PP-2A abolished the stimulatory effects of Ang II, AA, and 12S-HETE on neuronal I_K but did not alter Ang II-stimulated [³H]-AA release suggests that PP-2A is a distal event in this pathway.

Key words: angiotensin II; AT₂ receptor; delayed-rectifier K⁺ current; phospholipase A₂; arachidonic acid; lipoxygenase; serine and threonine phosphatase 2A; hypothalamus and brainstem neurons

	INTRODUCTION

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Mammalian brain contains angiotensin II (Ang II) type 2 (AT₂) receptors (Tsutsumi and Saavedra, 1991; Millan et al., 1992; Song et al., 1992), the functions of which are not well established. The fact that these sites are expressed in high levels in neonatal tissues has led to the idea that they have a role in development (Cook et al., 1991; Tsutsumi and Saavedra, 1991; Millan et al., 1992). Support for this has come from studies that determined that stimulation of AT₂ receptors causes neurite outgrowth in undifferentiated NG108-15 neuroblastoma × glioma cells (Laflamme et al., 1996) and causes apoptosis of pheochromocytoma PC-12W cells and R3T3 fibroblasts (Yamada et al., 1996; Horiuchi et al., 1997). Within the brain, blockade of periventricular AT₂ receptors potentiates the Ang II type 1 (AT₁) receptor-mediated stimulation of drinking and vasopressin secretion (Hohle et al., 1995), suggesting that AT₁ and AT₂ receptors may be antagonistic. In addition, mutant mice lacking the gene encoding the AT₂ receptor displayed decreased exploratory behavior and spontaneous movements compared with wild-type mice (Hein et al., 1995; Ichiki et al., 1995). Thus, AT₂ receptors may be involved in the central control of certain behaviors and hormone secretion, as well as having putative roles in apoptosis and differentiation.

Similar to the in vivo situation, neurons cultured from the hypothalamus and brainstem of newborn rats contain high levels of AT₂ receptors (Sumners et al., 1991), and we have used these cultures to determine the AT₂ receptor-mediated effects of Ang II on membrane K⁺ currents. The rationale for this approach was that changes in these currents form the basis of changes in neuronal activity and ultimately of behavioral and physiological effects. We determined that Ang II, via AT₂ receptors, stimulates neuronal delayed-rectifier K⁺ current (I_K) and transient K⁺ current (I_A) (Kang et al., 1993), effects mediated by an inhibitory G-protein (G_i) and abolished by inhibition of serine and threonine phosphatase 2A (PP-2A) (Kang et al., 1994). Our present investigations have centered around the possibility that phospholipase A₂ (PLA₂) is involved, because Ang II, via AT₂ receptors, causes stimulation of PLA₂ activity in certain cell types (Lokuta et al., 1994; Jacobs and Douglas, 1996). PLA₂ catalyzes the generation of arachidonic acid (AA) from membrane phospholipids, and AA and its metabolites such as hydroxyeicosatetraenoic acid (HETE), leukotrienes, and prostaglandins are known modulators of neuronal K⁺ channels (Premkumar et al., 1990; Schweitzer et al., 1993; Zona et al., 1993; Meves, 1994; Gubitosi-Klug et al., 1995; Kim et al., 1995). Furthermore, modulation of K⁺ currents in sympathetic neurons and pituitary tumor cells involves lipoxygenase (LO) metabolites of AA and serine and threonine phosphatases (Duerson et al., 1996; Yu, 1995). The data presented here indicate that the AT₂ receptor-mediated stimulation of neuronal I_K by Ang II involves an intracellular pathway that includes PLA₂, AA, and LO metabolites of AA. In addition, the results suggest that PP-2A may be important for the stimulation of neuronal I_K produced by Ang II and AA.

	MATERIALS AND METHODS

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Materials. Newborn Sprague Dawley rats were obtained from our breeding colony, which originated from Charles River Laboratories (Wilmington, MA). DMEM and TRIzol reagent were obtained from GIBCO-BRL (Gaithersburg, MD). Plasma-derived horse serum (PDHS) was from Central Biomedia (Irwin, MO). [5,6,8,9,11,12,14,15-³H]Arachidonic acid ([³H]-AA; specific activity of 203 Ci/mmol) and [1-³H]ethan-1-ol-2-amine HCL ([³H]ethanolamine; specific activity of 18.0 Ci/mmol) were purchased from Amersham (Arlington Heights, IL). Losartan potassium was generously provided by Merck (Darmstadt, Germany). PD123,319, nodularin (NDL), and antiflammin-2 were purchased from Research Biochemicals (Natick, MA). AA was from Calbiochem (La Jolla, CA). Polyclonal anti-phospholipase A₂ (anti-PLA₂) antibodies were purchased from Upstate Biotechnology (Lake Placid, NY). Activated silicic acid (200-325 mesh; Unisil) was from Clarkson Chemical (Williamsport, PA). Gene-Amp reverse transcriptase (RT)-PCR kits and all reagents for RT-PCR were purchased from Perkin-Elmer (Norwalk, CT). Bovine serum albumin (BSA), Ang II, tetrodotoxin (TTX), dipotassium ATP, sodium GTP, pertussis toxin (PTX), cadmium chloride (CdCl₂), HEPES, phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylserine (PS), phosphatidylinositol (PI), 4-bromophenacyl bromide (4-BPB), nordihydroguiaretic acid (NDGA), indomethacin, and 12S-hydroxy-(5Z,8Z,10E,14Z)-eicosatetraenoic acid (12S-HETE) were purchased from Sigma (St. Louis, MO). All other chemicals were purchased from Fisher Scientific (Houston, TX) and were of analytical grade or higher. Oligonucleotide primers for the rat brain cytosolic PLA₂ gene (Owada et al., 1994) and the rat AT₂ receptor gene (Mukoyama et al., 1993) were synthesized in the DNA core facility of the Interdisciplinary Center for Biotechnology Research, University of Florida. The sequences of these primers are as follows: PLA₂ gene, sense: 5-GCTCCACATGGTACATGTCA-3; antisense, 5-CTTCAAGCTACTCAAGGTCG-3; AT₂ receptor gene, sense, 5-ACCTGCATGAGTGTCGATAG-3; antisense: 5- GGATAGACAAGCCATACACC-3.

Preparation of cultured neurons. Neuronal cocultures were prepared from the brainstem and a hypothalamic block of newborn Sprague Dawley rats exactly as described previously (Sumners et al., 1991). Cultures were grown in DMEM and 10% PDHS for 10-14 d, at which time they consisted of ~90% neurons and ~10% astrocyte glia and microglia, as determined by immunofluorescent staining (Sumners et al., 1994).

Analysis of PLA₂ activity. Stimulation of PLA₂ activity results in generation of AA and of a lysophospholipid, and so we analyzed the effects of Ang II on the generation of both AA and lysophosphatidylethanolamine (LPE) as an index of PLA₂ activity. The generation of AA was analyzed as the release of [³H]-AA from neuronal membrane phospholipids, essentially as described by Wakelam and Currie (1992). In preliminary experiments we demonstrated that preincubation of cultured neurons with [³H]-AA (1.0 µCi/well) for 24 hr at 37°C resulted in equilibrium incorporation of the [³H]-AA into PE, PC, PS, and PI, as determined using thin layer chromatography (TLC) on silica gel 60 plates with a solvent of chloroform:methanol:glacial acetic acid:water (75:45:3:1). This time point was used in all subsequent experiments.

For the analyses of AA generation, we measured the release of [³H]-AA into the incubation medium from neurons that had been prelabeled with [³H]-AA for 24 hr in DMEM and 10% PDHS. The medium containing [³H]-AA was removed from the cells, which were then washed 3 times with 0.5 ml of Hank's Balanced Glucose (HBG) solution containing (in mM): 137 NaCl, 5.36 KCl, 1.66 MgSO₄, O.49 MgCl₂, 1.26 CaCl₂, 0.35 Na₂HPO₄, 4.17 NaHCO₃, and 10 glucose and 1% BSA, pH 7.4. The final wash of HBG was removed and replaced with 0.5 ml of HBG containing control solution, Ang II, or drugs for 1-5 min. Next, the incubation medium was removed from each well and underwent chloroform and methanol extraction, followed by isolation of the [³H]-AA using silicic acid adsorption chromatography (Wakelam and Currie, 1992). The amount of AA released into the medium was expressed as [³H]-AA released (dpm/well).

The generation of LPE was analyzed as the production of [³H]-LPE from [³H]-PE. Cultured neurons were preincubated with [³H]ethanolamine (2.0 µCi/well) for 48 hr at 37°C in DMEM and 10% PDHS, conditions that produced equilibrium incorporation into [³H]-PE. After this, the medium containing [³H]ethanolamine was removed, and the cells were washed 3 times with 0.5 ml of HBG and then incubated with control solution (HBG) or Ang II for 0.5-2.0 min. Next, the incubation medium was discarded, and the cellular [³H]-LPE content was analyzed as detailed by Wakelam and Currie (1992). Briefly, cells underwent chloroform and methanol extraction, followed by isolation of the [³H]-LPE using TLC (chloroform:methanol:glacial acetic acid:water; 50:30:8:3). Spots corresponding to [³H]-LPE were removed, and the data were expressed as dpm [³H]-LPE/well.

Electrophysiological recordings. Macroscopic K⁺ current was recorded using the whole-cell configuration of the patch-clamp technique as described previously (Hamill et al., 1981; Kang et al., 1994). Experiments were performed at room temperature (22-23°C) using an Axopatch-1D amplifier and Digidata 1200A interface (Axon Instruments, Burlingame, CA). Neurons were bathed in modified Tyrode's solution containing (in mM): 140 NaCl, 5.4 KCl, 2.0 CaCl₂, 2.0 MgCl₂, 0.3 NaH₂PO₄, 10 HEPES, 0.0001 TTX, 0.1 CdCl₂, and 10 dextrose, pH 7.4 (NaOH). The patch electrodes had resistances of 3-4 M when filled with an internal pipette solution containing (in mM): 140 KCl, 2 MgCl₂, 5 EGTA, 4 ATP, 0.1 GTP, 10 dextrose, and 10 HEPES, pH 7.2 (KOH). For whole-cell recordings, cell capacitance was canceled electronically, and the series resistance (<10 M) was compensated for by 75-80%. Data acquisition and analysis were performed using pCLAMP 6.03. Whole-cell currents were digitized at 3 kHz and filtered at 1 kHz (3 dB frequency filter). The current measurements from which mean current densities were derived were made 50 msec after the initiation of the test pulse, at which time the current measurements reflect only I_K (Kang et al., 1994). Current density was reported as pA/pF. The average cell capacitance for neurons used in this study was 33.9 ± 13.7 pF.

Extraction of total RNA and RT-PCR. Growth media were removed from cultured neurons that were then washed once with ice-cold Tyrode's solution, pH 7.4. After this, neurons were lysed in TRIzol reagent (0.5 ml/dish), and total RNA was extracted as detailed previously (Huang et al., 1997). For the experiments using neurons from the whole dish, RT-PCR of the AT₂ receptor and PLA₂ was performed using Gene-Amp RT-PCR kits essentially as described by Huang et al. (1997). In brief, PCR was performed at 94°C for 4 min, followed by 38 cycles at 94°C for 45 sec, 63°C (for PLA₂) or 62°C (for AT₂ receptor) for 1 min 40 sec, and 72°C for 2 min. After final extension at 72°C for 10 min, PCR products were electrophoresed on a 2% agarose gel containing 1 µg/ml ethidium bromide. Using these conditions, we observed the production of a 263 bp PLA₂-specific DNA and a 117 bp AT₂ receptor-specific DNA from the PCR, which correspond to the PLA₂ and AT₂ receptor mRNAs, respectively.

For the experiments using single neurons, RT-PCR of the AT₂ receptor and PLA₂ was performed using the following procedures. Using the electrophysiological methods described above, whole-cell recordings of I_K were made from neurons superfused with Ang II. For these recordings, the glass patch pipettes were washed once in ethanol and 3 times in distilled water and were then autoclaved for 30 min. Pipettes were then dried at 200°C for 1.5 hr. These patch pipettes were kept in a sealed box under vacuum until used for recordings. After the recordings of I_K, the neuronal intracellular contents were drawn into the tip of the patch pipette using negative pressure, and the tip was then broken off inside an RT-PCR tube. The volume of patch pipette solution and intracellular contents in the broken tip was ~6.5 µl, and this was adjusted to 8 µl with patch pipette solution for the RT-PCR, which was performed using Gene-Amp RT-PCR kits. A first PCR was performed exactly as described previously for neurons from the whole dish. A second PCR was performed (on 20 µl of the first PCR products) at 94°C for 4 min, followed by 30 cycles (for PLA₂) or 36 cycles (for AT₂ receptor) at 94°C for 45 sec, 63°C (for PLA₂) or 62°C (for AT₂ receptor) for 1 min 40 sec, and 72°C for 2 min. After final extension at 72°C for 10 min, the PCR products were electrophoresed on a 2% agarose gel containing 1 µg/ml ethidium bromide. Using these conditions for single cell RT-PCR, we observed the production of 263 bp PLA₂- and 117 bp AT₂ receptor-specific DNAs, similar to the bands obtained when using neurons from the whole dish. In all situations, exclusion of either RNA or murine leukemia virus reverse transcriptase resulted in no visible bands after gel electrophoresis.

Drug applications. Ang II, drugs, and anti-PLA₂ antibodies were dissolved in the appropriate solvent and then diluted in HBG (for the [³H]-AA and [³H]-LPE analyses) or in superfusate solution, patch pipette solution, or DMEM (for the electrophysiological experiments). In all experiments, solvent controls were performed for each protocol.

Experimental groups and data analysis. For individual [³H]-AA and [³H]-LPE analyses, each data point was obtained from four and three wells, respectively. Electrophysiological analyses were performed with the use of multiple 35 mm dishes of neurons. Comparisons were made with the use of a one-way ANOVA followed by the Newman-Keuls test to assess statistical significance.

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

Ang II stimulates PLA₂ activity in cultured neurons

As stated in the Materials and Methods, the effects of Ang II on the generation of AA and LPE were used as an index of stimulation of PLA₂ activity. In preliminary experiments, we determined that Ang II (100 nM; 1-5 min) stimulates release of radiolabel from cultured neurons that had been preincubated with [³H]-AA (1.0 µCi/well) (data not shown). This suggested that Ang II caused release of [³H]-AA, and in subsequent experiments, this was tested by performing silicic acid chromatography of the media extracts. Incubation of cultured neurons with control solution (HBG) for 1-5 min resulted in increasing amounts of [³H]-AA released as a function of time (Fig. 1A). Inclusion of Ang II (100 nM) in the incubation media resulted in a significant increase in the levels of [³H]-AA released at all time points (Fig. 1A). In an additional set of experiments, we determined that incubation of cultured neurons with Ang II (100 nM; 0.5-2 min) elicited a significant time-dependent stimulation of [³H]-LPE production (Fig. 1B). Taken together, the data presented in Figure 1, A and B, indicate that Ang II stimulates PLA₂ activity in cultured neurons. The stimulatory effects of Ang II (100 nM) on [³H]-AA release from cultured neurons were significantly reduced (by ~73%) by the addition of the selective AT₂ receptor blocker PD123,319 (PD; 1 µM) to the incubation media (Fig. 1C). By contrast, the AT₁-selective receptor antagonist losartan (Los; 1 µM) reduced the stimulatory effects of Ang II on [³H]-AA release by ~30% (Fig. 1C). Combined incubations with both PD (1 µM) and Los (1 µM) resulted in complete inhibition of the effects of Ang II (data not shown). Neither PD nor Los alone had significant effects on [³H]-AA release (Fig. 1C). These data indicate that both AT₂ and AT₁ receptors are involved in Ang II-stimulated [³H]-AA release from cultured neurons. Because the majority of AT₁ and AT₂ receptors in these cultures are present on different neurons (Gelband et al., 1997), it is probable that the AT₁ and AT₂ receptor-mediated effects of Ang II on AA release are on different cells. In the presence of 1 µM Los, to block AT₁ receptors, the stimulation of [³H]-AA release by Ang II (100 nM) was completely abolished by pretreatment of cultured neurons with the selective PLA₂ inhibitor 4-BPB (10 µM; 30 min) (Fig. 1D). These data suggest that the AT₂ receptor-mediated component of Ang II-stimulated [³H]-AA release is attributable to activation of PLA₂.

View larger version (27K): [in this window] [in a new window]   Figure 1.   Ang II stimulates PLA2 activity in cultured neurons. A, Cultured neurons were prelabeled with [3H]-AA (1.0 µCi/well) for 24 hr at 37°C and then incubated with 0.5 ml of HBG/well in the absence (; control) or presence () of 100 nM Ang II for the indicated times at 37°C. This was followed by analysis of [3H]-AA release into the growth media as detailed in the Materials and Methods. Data are mean ± SEM from four experiments; *, significantly different from controls, p < 0.05. B, Cultured neurons were prelabeled with [3H]-ethanolamine (2.0 µCi/well) for 48 hr at 37°C and then incubated with 0.5 ml of HBG in the absence (Con) or presence of 100 nM Ang II for the indicated times at 37°C. This was followed by analysis of cellular [3H]-LPE as detailed in the Materials and Methods. Data are mean ± SEM from four experiments and are presented as a percent of control (100%). Control cellular [3H]-LPE was 2258 ± 279 dpm/well; *, significantly different from Con, p < 0.05. C, Cultured neurons that had been prelabeled with [3H]-AA as described above were incubated with 0.5 ml of HBG/well in the absence (CON) or presence of either 100 nM Ang II, Ang II plus 1 µM PD, Ang II plus 1 µM Los, PD, or Los for 2 min at 37°; analysis of [3H]-AA release into the growth media followed. Data are mean ± SEM from five experiments; *, significantly different from control, p < 0.05; ++Significantly different from Ang II-treated cells, p < 0.05. D, Cultured neurons that had been prelabeled with [3H]-AA as described above were preincubated with 4-BPB (10 µM; 30 min), PTX (200 ng/ml; 24 hr), or control solvent. After this, control and drug-treated cultures were incubated with 100 nM Ang II for 2 min at 37°C. All incubations were performed in the presence of 1 µM Los and were followed by analysis of [3H]-AA release into the growth media. Data are mean ± SEM from three (4-BPB) and four (PTX) experiments; *significantly different from control, p < 0.05; ++, significantly different from Ang II-treated neurons, p < 0.05.

In previous studies, we had determined that neuronal AT₂ receptors couple to a stimulation of I_K via a PTX-sensitive inhibitory G-protein (G_i) (Kang et al., 1994). Therefore, we tested the effects of PTX, which inhibits both G_i and G_o, on Ang II-stimulated [³H]-AA release. Preincubation of cultured neurons with PTX (200 ng/ml; 24 hr) completely abolished the stimulation of [³H]-AA release produced by Ang II (100 nM) in the presence of 1 µM Los (Fig. 1D). These data provide indirect support for the idea that the AT₂ receptor-mediated stimulation of [³H]-AA release by Ang II involves a G_i protein.

Stimulation of neuronal I_K by Ang II involves PLA₂ and AA

In previous studies, we determined that selective stimulation of neuronal AT₂ receptors caused an increase in I_K (Kang et al., 1993), whereas selective stimulation of neuronal AT₁ receptors caused a decrease in I_K (Sumners et al., 1996). Because some neurons in these cultures contain both AT₁ and AT₂ receptors, with potentially offsetting effects on I_K (Gelband et al., 1997), all of the present electrophysiological studies on AT₂ receptors were performed in the presence of the AT₁ receptor blocker Los (1 µM). Los did not alter baseline I_K. In the present studies, superfusion of cultured neurons with Ang II (100 nM) caused a significant stimulation of I_K that was completely inhibited by 1 µM PD123,319 (Fig. 2), in agreement with our previous experiments (Kang et al., 1993). Treatment of cultured neurons with PLA₂ inhibitors significantly attenuated the AT₂ receptor-mediated stimulation of I_K by Ang II. For example, pretreatment with 4-BPB (10 µM; 30 min) or inclusion of antiflammin-2 (20 µM) in the pipette solution resulted in a 70-76% inhibition of Ang II-stimulated I_K (Fig. 2). Furthermore, intracellular perfusion of anti-PLA₂ antibodies (1:1250) caused an ~76% inhibition of Ang II-stimulated I_K (Fig. 2). These effects of 4-BPB, antiflammin-2, and anti-PLA₂ antibodies were maximal and specific, i.e., higher concentrations produced no greater inhibition of Ang II-stimulated I_K (data not shown). Control recordings in the presence of these inhibitors were not significantly different compared with control recordings of I_K from untreated neurons (Fig. 2). The data presented in Figure 2 therefore indicate that PLA₂ is involved in the AT₂ receptor-mediated stimulation of I_K by Ang II. If this is the case, it follows that the Ang II-responsive neurons should contain PLA₂. This was tested by performing single-cell RT-PCR analyses of PLA₂ mRNA in neurons that responded to Ang II with an increase in I_K. The data in Figure 3, A and B, demonstrate the presence of AT₂ receptor mRNA in neurons from the whole dish and in a single neuron that responded to Ang II (100 nM) with an increase in I_K. Furthermore, Figure 3, C and D, demonstrates the presence of PLA₂ mRNA in neurons from the whole dish and in a single neuron that exhibited an AT₂ receptor-mediated increase in I_K elicited by Ang II (100 nM).

View larger version (22K): [in this window] [in a new window]   Figure 2.   Stimulation of neuronal IK by Ang II via AT2 receptors: effect of PLA2 inhibitors. IK was recorded during 100 msec voltage steps from a holding potential of 80 to +10 mV. Top, Representative current tracings showing the effects of superfused Ang II (100 nM) on IK in untreated (control) neurons (± 1 µM PD123,319) (1), in neurons pretreated with 10 µM 4-BPB for 30 min (2), in neurons perfused intracellularly with anti-PLA2 antibodies (1:1250; for procedures, see Zhu et al., 1997) (3), and in neurons pretreated with 20 µM antiflammin-2 for 20 hr (4). Control recordings (CON) in all sets of traces were made before application of Ang II. All recordings were made in the presence of 1 µM Los to block AT1 receptors. Bottom, Bar graphs showing mean ± SEM of current densities obtained in each treatment situation. Sample sizes were 15, 8, 7, and 6 neurons for the untreated, 4-BPB, anti-PLA2, and antiflammin-2 groups, respectively; *p < 0.001 compared with the respective control; ++p < 0.001 compared with Ang II alone (no 4-BPB, anti-PLA2, or antiflammin-2).

View larger version (16K): [in this window] [in a new window]   Figure 3.   Stimulation of neuronal IK by Ang II: presence of AT2 receptor mRNA and PLA2 mRNA in Ang II-responsive neurons. A, C, Current tracings from two neurons showing stimulation of IK (AT2 receptor-mediated) by 100 nM Ang II. IK was recorded as described in Figure 2. After these recordings, the neurons were prepared for single cell RT-PCR as detailed in the Materials and Methods. B, Ethidium bromide-stained gels showing the RT-PCR DNA products that correspond to the AT2 receptor mRNA (AT2-R; 117 bp). Lane 1, AT2-R mRNA from the responsive neuron shown in A. Lane 2, AT2-R mRNA obtained from a whole dish of neurons. Leftmost lane is 100 bp DNA ladder. D, Ethidium bromide-stained gels showing the RT-PCR products that correspond to the PLA2 mRNA (263 bp). Lanes 1, 2, PLA2 mRNA obtained from a whole dish of neurons. Lane 3, PLA2 mRNA from the responsive neuron shown in C. Rightmost lane is 100 bp DNA ladder.

Activation of PLA₂ results in generation of AA, and it is known that AA as well as some AA metabolites can modulate K⁺ currents and channels (Premkumar et al., 1990; Schweitzer et al., 1993; Zona et al., 1993; Meves, 1994; Gubitosi-Klug et al., 1995; Kim et al., 1995; Duerson et al., 1996; Yu, 1995). Therefore, if PLA₂ is involved in mediating the stimulatory effects of Ang II on I_K, then we might predict that AA would mimic the effects of Ang II. This was the case as superfusion of AA (10-100 µM) onto neurons produced a reversible and concentration-dependent stimulation of I_K (Fig. 4A,B). The stimulatory effects of both Ang II and AA on neuronal I_K were significantly reduced (by ~77%) by the pretreatment of cultures with the general LO inhibitor NDGA (5 µM) (Fig. 5A). By contrast, pretreatment with the cyclooxygenase inhibitor indomethacin (10 µM) did not alter the stimulation of neuronal I_K by Ang II (Fig. 5A) or by AA (data not shown). Higher concentrations of NDGA produced no further inhibition of Ang II-stimulated I_K. Control recordings in the presence of NDGA and indomethacin were not significantly different from control recordings of I_K in untreated neurons (Fig. 5A). These data suggest that the stimulatory actions of Ang II and AA on neuronal I_K are mostly mediated via LO metabolites of AA. This idea is supported by experiments that demonstrate that intracellular perfusion of 12S-HETE, a 12-lipoxygenase (12-LO) metabolite of AA, elicits a significant stimulation of neuronal I_K (Fig. 5B).

View larger version (12K): [in this window] [in a new window]   Figure 4.   AA stimulates IK in cultured neurons. IK was recorded as described in Figure 2. A, Representative current tracings and time course showing the effects of superfused AA (50 µM) on IK. Control (Con) recordings were made before application of AA. B, Effects of different concentrations of AA on IK. Data are mean ± SEM of percent stimulation of IK above control (0 on x-axis). Sample sizes were five to six neurons at each concentration; *significantly different from control, p < 0.001.

View larger version (24K): [in this window] [in a new window]   Figure 5.   Stimulation of neuronal IK by Ang II and AA: role of LO metabolites of AA. IK was recorded as described in Figure 2. A, Cultured neurons were pretreated with either control solvent (untreated), NDGA (5 µM), or indomethacin (10 µM) for 5 min at room temperature and then were superfused with control solution (superfusate; Con), 100 nM Ang II, or 50 µM AA. Data are mean ± SEM of current densities obtained in each treatment situation. For the Ang II data, sample sizes were 14, 6, and 7 neurons in the untreated, NDGA, and indomethacin groups, respectively. For the AA data, sample sizes were 9 and 7 neurons in the untreated and NDGA groups, respectively; *p < 0.001 compared with the respective control; ++p < 0.001 compared with Ang II or AA alone (no NDGA). B, Representative current tracings and time course show the effects of intracellular application of 12S-HETE (1 µM) on IK. Control (Con) recordings were made before the application of 12S-HETE, which was performed via an intracellular perfusion technique as detailed previously (Zhu et al., 1997). Bar graphs are mean ± SEM of IK values in Con and 12S-HETE-treated neurons. Sample size was seven neurons; *significantly different from control, p < 0.001.

Inhibition of PP-2A blocks the stimulatory effects of Ang II, AA, and 12S-HETE on neuronal I_K

Our previous studies suggested that the AT₂ receptor-mediated stimulation of I_K by Ang II was inhibited by low concentrations of the selective PP-2A inhibitor okadaic acid (Kang et al., 1994). This was confirmed in the present study by the demonstration that the PP-2A inhibitor nodularin (NDL) (Honkanen et al., 1991) completely reversed the stimulation of neuronal I_K by Ang II (100 nM) (Fig. 6A). The data presented in Figure 6A are from neurons pretreated with NDL (20 µM; 24 hr) or treated with NDL (2 µM) in the pipette solution. Similarly, pretreatment of cultured neurons with 20 µM NDL for 24 hr abolished the stimulation of neuronal I_K either by superfusion of AA (50 µM) or by intracellular perfusion of 12S-HETE (1 µM) (Figure 6B). These data support the idea that PP-2A is involved in the stimulatory effects of Ang II, AA, and 12S-HETE on I_K. In addition, the AA data suggest that PP-2A is involved at a locus distal to the generation of AA by PLA₂. This is supported by the fact that AT₂ receptor-mediated stimulation of [³H]-AA release by Ang II was not altered by NDL (20 µM; 24 hr pretreatment) (Fig. 7).

View larger version (27K): [in this window] [in a new window]   Figure 6.   Inhibition of PP-2A blocks the stimulatory effects of Ang II and AA on neuronal IK. IK was recorded as described in Figure 2. A, Neurons were superfused with control solution (superfusate; CON) or Ang II (100 nM) in the absence (untreated) or presence of NDL (either pretreatment with 20 µM NDL for 24 hr or inclusion of 2 µM NDL in the pipette solution). All recordings were made in the presence of a constant superfusion of 1 µM Los. Top, Representative current tracings show the effects of Ang II on IK in each treatment situation. Bottom, Bar graphs are mean ± SEM of the current densities in each treatment group. Sample sizes were 17, 6, and 5 neurons in the untreated, NDL (pretreatment), and NDL (pipette solution) groups, respectively; *p < 0.001 compared with respective control; ++, p < 0.001 compared with Ang II alone (no NDL). B, Neurons were superfused with control solution (superfusate; CON) or AA (50 µM) or were perfused intracellularly with control solution (patch pipette solution; Con) or 12S-HETE (1 µM). Application of AA and 12S-HETE was made in the absence (untreated) or presence of NDL (20 µM; pretreatment for 24 hr). Top, Representative current tracings show the effects of AA and 12S-HETE on IK in both treatment situations. Bottom, Bar graphs are mean ± SEM of current densities in the treatment groups. Sample sizes were 14 and 5 neurons for the untreated and NDL groups (AA superfusions), respectively. Sample sizes were 8 and 9 neurons for the untreated and NDL groups (12S-HETE application), respectively. *p < 0.001 compared with respective IK control value; ++, p < 0.001 compared with AA or 12S-HETE alone (no NDL).

View larger version (16K): [in this window] [in a new window]   Figure 7.   Ang II-stimulated [3H]-AA release from cultured neurons: effects of nodularin. Cultures were prelabeled with [3H]-AA (1.0 µCi/well) for 24 hr at 37°C. At the same time, cultures were also preincubated with control solvent or NDL (20 µM) for 24 hr. After this, control and NDL-treated cultures were incubated with 0.5 ml/well of HBG in the absence (CON) or presence of 100 nM Ang II for 2 min at 37°C. Incubations were performed in the presence of 1 µM Los. These incubations were followed by analysis of [3H]-AA release into the growth media as detailed in the Materials and Methods. Data are mean ± SEM from four independent experiments; *significantly different from control, p < 0.001.

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

The data presented here indicate that Ang II stimulates, via AT₁ and AT₂ receptors, production of AA in neurons cultured from newborn rat hypothalamus and brainstem. This demonstration is reasonable considering that activation of either AT₁ or AT₂ receptors elicits a stimulation of AA release in various peripheral cells (Lokuta et al., 1994; Rao et al., 1994; Jacobs and Douglas, 1996; Pueyo et al., 1996). Within cultured neurons, the majority of this Ang II response is mediated via AT₂ receptors (Fig. 1C), which is consistent with the demonstration that these cultures contain greater numbers of AT₂ receptors than AT₁ receptors (Sumners et al., 1991). Most of the AT₁ and AT₂ receptors in these cultures are located on different populations of neurons (Gelband et al., 1997), and so it is probable that these stimulatory actions of Ang II on AA release occur via AT₁ and AT₂ receptors located on different cells. The release of AA stimulated by Ang II may occur via various mechanisms. For example, we have determined previously that Ang II, via AT₁ receptors, stimulates phospholipase C, phosphoinositide hydrolysis, and production of diacylglycerol in cultured neurons (Sumners et al., 1994, 1996). It is well known that AA can be released from diacylglycerol via the action of diacylglycerol lipase (Irvine, 1982). Therefore, in the present study the AT₁ receptor-mediated effects of Ang II may occur via sequential activation of phospholipase C and diacylglycerol lipase (Irvine, 1982). By contrast, the AT₂ receptor-mediated stimulation of AA release in cultured neurons seems to occur via activation of PLA₂, because this effect was abolished by the selective PLA₂ inhibitor 4-BPB (Fig. 2A; Schweitzer et al., 1993; Williams et al., 1994). Our data also indicate that the Ang II-induced stimulation of AA release, via AT₂ receptors, is abolished by PTX (Fig. 1D). This is consistent with our previous observations that neuronal AT₂ receptors couple intracellularly via a PTX-sensitive G_i protein (Kang et al., 1994; Huang et al., 1995) and also with studies that have shown that the AT₂ receptor coprecipitates with G_i2 and G_i3 proteins (Zhang and Pratt, 1996). However, at present we have no indication whether the AT₂ receptor-mediated stimulation of AA release occurs via direct coupling of G_i to PLA₂ or via an indirect intracellular mechanism (Axelrod et al., 1988; Dickerson and Weiss, 1995).

The present studies also indicate that activation of PLA₂ and the subsequent generation of AA and LO metabolites of AA are involved in the AT₂ receptor-mediated stimulation of I_K by Ang II. Support for this comes from the fact that these Ang II-responsive neurons contain PLA₂, as evidenced by single-cell RT-PCR analyses and from the demonstration that PLA₂ inhibitors significantly attenuate the AT₂ receptor-mediated stimulation of neuronal I_K. However, the failure of PLA₂ inhibitors to abolish completely the stimulation of neuronal I_K by Ang II probably indicates that another mechanism or pathway is also involved. One possibility is that the neuronal AT₂ receptor can also influence I_K by direct membrane-delimited coupling between G_i subunits and the delayed-rectifier K⁺ channel that is involved. AA and LO metabolites of AA are known modulators of neuronal ionic currents and channels (Premkumar et al., 1990; Schweitzer et al., 1993; Zona et al., 1993; Meves, 1994; Gubitosi-Klug et al., 1995; Kim et al., 1995; Duerson et al., 1996; Yu, 1995), and their involvement in the stimulation of neuronal I_K by Ang II is suggested by a number of observations. First, both AA and 12S-HETE (a 12-LO metabolite of AA) elicit significant stimulatory effects on neuronal I_K similar to that obtained with Ang II via AT₂ receptors. Second, the stimulatory effects of Ang II and AA on neuronal I_K are significantly attenuated by inhibition of LO but not by inhibition of cyclooxygenases. The observation that LO inhibitors do not completely block these effects of Ang II and AA may suggest that the stimulation of I_K is partially mediated via a direct action of AA at the K⁺ channel, as shown in other systems (Schweitzer et al., 1993; Kim et al., 1995). Many questions remain to be answered concerning the roles of AA and LO metabolites in the stimulation of neuronal I_K by Ang II. For example, although our studies indicate that 12S-HETE stimulates neuronal I_K and is a possible candidate for mediating the stimulatory effects of Ang II on I_K, we cannot exclude the possibility that other LO metabolites (e.g., leukotrienes, 5-LO metabolites) are also involved. Furthermore, does AA directly modulate K⁺ channel activity?

The present results and our previous studies (Kang et al., 1994) demonstrate that inhibition of PP-2A blocks the stimulatory effects of Ang II, AA, and 12S-HETE on neuronal I_K, while not altering baseline I_K. The exact cellular locus at which PP-2A is involved is not known. However, the fact that Ang II-stimulated AA release (AT₂ receptor-mediated) is not affected by inhibition of PP-2A suggests that this enzyme may be involved as a distal event in the intracellular pathway controlling I_K. One possibility is that PP-2A is complexed or associated with the delayed-rectifier K⁺ channel (which underlies I_K) in the neuronal membrane. Support from this idea comes from studies that demonstrated that BK_Ca channels from rat brain exist as part of a regulatory complex with PP-1 (Reinhart and Levitan, 1995) and that a PP-2A-sensitive regulatory site controls the gating of L-type Ca²⁺ channels in smooth muscle cells (Groschner et al., 1996). The exact locus of the involvement of PP-2A will only be determined by single-channel recordings. Because there is much evidence that the phosphorylation and dephosphorylation of channel proteins is extremely important in the regulation of ion channel activity (Levitan, 1994), another question that remains is whether PP-2A directly modulates the activity of the K⁺ channel(s) that underlie I_K by dephosphorylation.

In summary, our data provide the first demonstration that an intracellular pathway that includes activation of PLA₂ and generation of AA and LO metabolites of AA is important for the stimulation of neuronal I_K by Ang II via AT₂ receptors. Furthermore, our data suggest that the activation of PP-2A may be a distal event in this pathway. Interestingly, similar pathways have been proposed for calcium-dependent modulation of M (K⁺) current in sympathetic neurons (Yu, 1995) and for somatostatin-induced stimulation of BK_Ca in rat pituitary tumor cells (Duerson et al., 1996). Collectively, these findings may suggest that a common series of intracellular events (AA/LO metabolites/PP-2A) may be responsible for the modulation of different K⁺ currents in different cell types.

	FOOTNOTES

Received Aug. 21, 1997; revised Oct. 27, 1997; accepted Nov. 4, 1997.

This work was supported by National Institutes of Health Grants NS19441, HL49130, and HL52189. We thank Jennifer Brock for typing this manuscript.

Correspondence should be addressed to Dr. Colin Sumners, Department of Physiology, University of Florida, Box 100274, 1600 Southwest Archer Road, Gainesville, FL 32610. 

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