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Abstract

Intracellular Ca²⁺ plays a fundamental role in regulating cell functions in pulmonary arterial smooth muscle cells (PASMCs). A rise in cytosolic Ca²⁺ concentration ([Ca²⁺]_cyt) triggers pulmonary vasoconstriction and stimulates PASMC proliferation. [Ca²⁺]_cyt is increased mainly by Ca²⁺ release from intracellular stores and Ca²⁺ influx through plasmalemmal Ca²⁺-permeable channels. Given the high concentration of intracellular Cl⁻ in PASMCs, Ca²⁺-activated Cl⁻ (Cl_Ca) channels play an important role in regulating membrane potential and cell excitability of PASMCs. In this study, we examined whether activity of Cl_Ca channels was involved in regulating [Ca²⁺]_cyt in human PASMCs via regulating receptor- (ROCE) and store- (SOCE) operated Ca²⁺ entry. The data demonstrated that an angiotensin II (100 nM)-mediated increase in [Ca²⁺]_cyt via ROCE was markedly attenuated by the Cl_Ca channel inhibitors, niflumic acid (100 µM), flufenamic acid (100 µM), and 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid (100 µM). The inhibition of Cl_Ca channels by niflumic acid and flufenamic acid significantly reduced both transient and plateau phases of SOCE that was induced by passive depletion of Ca²⁺ from the sarcoplasmic reticulum by 10 µM cyclopiazonic acid. In addition, ROCE and SOCE were abolished by SKF-96365 (50 µM) and 2-aminoethyl diphenylborinate (100 µM), and were slightly decreased in the presence of diltiazem (10 µM). The electrophysiological and immunocytochemical data indicate that Cl_Ca currents were present and TMEM16A was functionally expressed in human PASMCs. The results from this study suggest that the function of Cl_Ca channels, potentially formed by TMEM16A proteins, contributes to regulating [Ca²⁺]_cyt by affecting ROCE and SOCE in human PASMCs.

Keywords

angiotensin II niflumic acid TMEM16A

INTRODUCTION

In pulmonary artery smooth muscle cells (PASMCs), cytosolic Ca²⁺ concentration ([Ca²⁺]_cyt) is mainly regulated by a balance of Ca²⁺ release from intracellular stores and Ca²⁺ influx through plasmalemmal Ca²⁺-permeable channels, as well as Ca²⁺ sequestration into intracellular stores by the Ca²⁺-Mg²⁺ ATPase on the sarcoplasmic/endoplasmic reticulum membrane (SERCA) and Ca²⁺ extrusion via the Ca²⁺-Mg²⁺ ATPase and Na⁺/Ca²⁺ exchanger on the plasma membrane.^[1,2] PASMCs functionally express various Ca²⁺-permeable channels including (a) voltage-dependent Ca²⁺ channels (VDCCs) that are activated by membrane depolarization,^[3] and (b) receptor-operated Ca²⁺ (ROC) channels that are stimulated and activated by vasoconstrictors, such as endothelin-1,^[4] serotonin,^[5] phenylephrine,^[6] and histamine,^[7] and by growth factors, including epidermal growth factor^[8] and platelet-derived growth factor.^[9] The activation of ROC channels by interaction between ligands and membrane receptors results in receptor-operated Ca²⁺ entry (ROCE) that greatly contributes to increases in [Ca²⁺]_cyt in PASMCs exposed to vasoconstrictors and growth factors.^[1,10,11] PASMCs also possess (c) store-operated Ca²⁺ (SOC) channels that are opened by the depletion of Ca²⁺ from the sarcoplasmic reticulum (SR), which leads to capacitative Ca²⁺ entry, or store-operated Ca²⁺ entry (SOCE). SOCE is an important mechanism involved in maintaining a sustained elevation of [Ca²⁺]_cyt and refilling Ca²⁺ into the depleted SR.^[1,10–12] We showed previously that increased Ca²⁺ influx through SOC or SOCE contributes to stimulating PASMC proliferation; inhibition of SOCE significantly attenuated growth factor-mediated PASMC proliferation. These results suggest that SOCE plays a significant role in regulating proliferation in vascular smooth muscle cells.^[9,13,14]

It has been well demonstrated that the activity of Ca²⁺-activated Cl⁻ (Cl_Ca) channels play an important role in regulating contraction, migration, and apoptosis in many cell types.^[15,16] In vascular smooth muscle cells, Cl_Ca channels are activated by a rise in [Ca²⁺]_cyt following agonist-induced Ca²⁺ release from the SR through inositol-1,4,5-trisphosphate receptors (IP₃Rs). In addition, the activation of Cl_Ca channels is evoked by spontaneous Ca²⁺ release through ryanodine receptors in the SR and is responsible for eliciting spontaneous transient inward currents in several types of vascular smooth muscle cells. The intracellular Cl⁻ concentration in vascular smooth muscle cells (including PASMCs) is estimated to be 30 to 60 mM,^[15–17] so the reversal potential for Cl⁻ is supposed to be much less negative (ranging from −20 to −30 mV) than that for K⁺ (approximately −80 mV). Therefore, an increase in Cl⁻ conductance in PASMCs under these conditions would generate inward currents (due to Cl⁻ efflux) and cause membrane depolarization which subsequently induces Ca²⁺ influx by opening VDCCs and ultimately results in vasoconstriction. The molecular composition of Cl_Ca channels in vascular smooth muscle cells (including PASMCs), however, is not fully identified. Recently, a transmembrane protein encoded by TMEM16A gene has been demonstrated to form Cl_Ca channels in vascular smooth muscle cells.^[18–20]

In this study, we examined whether Cl_Ca channel activity was involved in the regulation of [Ca²⁺]_cyt via ROCE and SOCE in human PASMCs using digital imaging fluorescence microscopy. We also examined the functional expression of Cl_Ca channels (TMEM16A) in human PASMCs using electrophysiological and immunocytochemical approaches.

MATERIALS AND METHODS

Cell culture

Human PASMCs (passage 5 to 10) from normal subjects were purchased from Lonza (Walkersville, MD) Cells were cultured in Medium 199 (Invitrogen-GIBCO, Grand Island, NY) supplemented with 10% fetal bovine serum (Invitrogen-GIBCO), 100 U/ml penicillin plus 100 µg/ ml streptomycin (Invitrogen-GIBCO), 50 µg/ml D-valine (Sigma-Aldrich, St. Louis, MO), and 20 µg/ml endothelial cell growth supplement (BD Biosciences, Franklin Lakes, NJ) at 37°C. All cells were incubated in a humidified 5% CO₂ atmosphere at 37°C. After reaching confluence, the cells were sub-cultured by trypsinization with 0.05% trypsin-EDTA (Invitrogen-GIBCO), plated onto 25-mm cover slips (Fisher Scientific, Pittsburgh, PA). and incubated at 37°C for 1–3 days before electrophysiological and fluorescence microscopy experiments.

[Ca²⁺]_cyt measurement

Human PASMCs cultured on 25-mm cover slips were placed in a recording chamber on the stage of an invert fluorescent microscope (Eclipse Ti-E; Nikon, Tokyo, Japan) equipped with an objective lens (S Plan Fluor 20×/0.45 ELWD; Nikon) and an EM-CCD camera (Evolve; Photometrics, Tucson, AZ). [Ca²⁺]_cyt was monitored using a membrane-permeable Ca²⁺-sensitive fluorescent indicator, fura-2 acetoxymethyl ester (fura-2/AM; Invitrogen-Molecular Probes, Eugene, OR) and imaged with NIS Elements 3.2 software (Nikon). Cells were loaded by incubation in HEPES-buffered solution containing 4 µM fura-2/AM for 60 min. at room temperature (25°C). The loaded cells were then washed with HEPES-buffered solution for 10 min. to remove excess extracellular indicator and allow sufficient time for intracellular esterase to cleave acetoxymethyl ester from fura-2. Cells were then excited at 340-nm and 380-nm wavelengths (D340×v2 and D380×v2 filters, respectively; Chroma Technology, Bellows Falls, VT) by a xenon arc lamp (Lambda LS; Sutter Instrument, Novato, CA) and an optical filter changer (Lambda 10-B; Sutter Instrument). Emission of Fura-2 was collected through a dichroic mirror (400DCLP; Chroma Technology) and a wide band emission filter (D510/80m; Chroma Technology). [Ca²⁺]_cyt within a region of interest (5×5 µm) that was placed at the peripheral region of each cell was measured as the ratio of fluorescence intensities (F₃₄₀/F₃₈₀) every 2 sec. The HEPES-buffered solution had an ionic composition of 137 mM NaCl, 5.9 mM KCl, 2.2 mM CaCl₂, 1.2 mM MgCl₂, 14 mM glucose, and 10 mM HEPES. The pH was adjusted to 7.4 with 10 N NaOH. The external Ca²⁺-free solution was prepared by removing extracellular CaCl₂ and adding 1 mM EGTA (to chelate the residual Ca²⁺ in the bath solution). The recording chamber was continuously perfused with HEPES-buffered solution at a flow rate of 2 ml/min. using a mini-pump (Model 3385; Control, Friendswood, TX). [Ca²⁺]_cyt measurements were carried out at 32°C using an automatic temperature controller (TC-344B, Warner Instruments, Holliston, MA).

Electrophysiological recording

The whole-cell Cl_Ca current in a single PASMC was recorded using the patch-clamp technique with an Axopatch-1D amplifier (Molecular Devices-Axon, Foster City, CA), an analog-digital converter (Digidata 1200; Molecular Devices-Axon), and pCLAMP 8 software (Molecular Devices-Axon). The extracellular (bath) solution had an ionic composition of 137 mM NaCl, 10 mM tetraethylammonium (TEA) chloride, 5 mM 4-aminopyridine (4-AP), 2.2 mM CaCl₂, 1.2 mM MgCl₂, 14 mM glucose, and 10 mM HEPES. The pH was adjusted to 7.4 with 10 N NaOH. The low Cl⁻ concentration solution was prepared by substituting 117 mM NaCl of the extracellular solution with the equal molar of sodium gluconate. The pipette (intracellular) solution contained 120 mM CsCl, 20 mM TEA chloride, 4.3 mM CaCl₂, 2.8 mM MgCl₂, 2 mM Na₂ATP, 10 mM HEPES, and 5 mM EGTA. The pCa was fixed to 6.0, which was estimated by the Maxchelator program (http://www.stanford.edu/∼cpatton/maxc.html). The pH was adjusted to 7.2 with 1 N CsOH. The recording chamber was continuously superfused with extracellular solution at a flow rate of 2 ml/min. using a perfusion system (VC-6; Warner Instrument, Hamden, CT). Electrophysiological recordings were carried out at room temperature (25°C).

Immunocytochemical staining

Cultured cells on 35-mm culture dishes with 14-mm glass bottom (MatTek, Ashland, MA) were fixed with 4% paraformaldehyde in Dulbecco's phosphate buffered saline (DPBS; Invitrogen-GIBCO) for 10 min. at room temperature (25°C). Excessive paraformaldehyde was removed thoroughly with DPBS. The cells were then treated with DPBS containing 0.2% Triton X-100, 1% normal goat serum (Dako Denmark, Glostrup, Denmark), and TMEM16A antibody (pre-diluted, ab53213, Abcam, Cambridge, MA; or 1:100 dilution, ab53212, Abcam) for 12 hr. at 4°C. After washing repeatedly in DPBS, the cells were covered with DPBS containing 0.2% Triton X-100, 1% normal goat serum, and Alexa Fluor 488-labeled secondary antibody (1:100 dilution; Invitrogen-Molecular Probes) for 1 hr. at room temperature and then rinsed with DPBS. Then cells were mounted in VECTASHIELD hard-set mounting medium with 4′,6-diamidino-2-phenylindole (DAPI, 1.5 µg/ml) (Vector Laboratories, Burlingame, CA) and placed on the stage of an invert fluorescent microscope (Eclipse Ti-E; Nikon) equipped with an objective lens (Plan Apo 60×/1.40 oil immersion; Nikon), a CCD camera (CoolSNAP ES²; Photometrics), and NIS Elements 3.2 software (Nikon). Immunocytochemical images were obtained using the specific filter sets for DAPI (Ex340-380/DM400/Em435-485; Chroma Technology) and Alexa Fluor 488 (Ex460-500/DM505/Em510-560; Chroma Technology).

Drugs

Pharmacological reagents were obtained from Sigma-Aldrich. All hydrophobic compounds were dissolved in dimethyl sulfoxide (DMSO) at the concentration of 10 or 100 mM as a stock solution. It was confirmed that up to 0.1 % of DMSO did not affect these responses.

Statistical analysis

Pooled data are shown as the mean±SE. The statistical significance between two groups was determined by Student's t-test. The statistical significance among groups was determined by Scheffé's test after one-way analysis of variance. Significant difference is expressed in the figures as *P<0.05 or **P<0.01.

RESULTS

Inhibition of agonist-induced Ca²⁺ influx or ROCE by Cl_Ca channel blockers in human PASMCs

The increase in [Ca²⁺]_cyt evoked by agonist stimulation was imaged in human PASMCs loaded with 4 μM fura-2/AM and quantitated in arbitrary units (au) by the change in F₃₄₀/F₃₈₀ ratio. Short-term application (2 min.) of 100 nM angiotensin II induced a transient increase in [Ca²⁺]_cyt (by 0.49±0.01 au, n=150) (Figs. 1 and 2). The angiotensin II-induced [Ca²⁺]_cyt increase was attenuated by 100 μM niflumic acid, a fenamate compound that is most frequently used as a blocker of Cl_Ca channels (from 0.51±0.03 to 0.13±0.02 au, n=29, P<0.01) (Fig. 1a and d). The inhibitory effect of niflumic acid on the angiotensin II-mediated increase in [Ca²⁺]_cyt was reversible upon washout (0.42±0.04 au, n=29). Pretreatment with 100 μM flufenamic acid, another fenamate compound that blocks Cl_Ca channels, markedly reduced the angiotensin II-induced [Ca²⁺]_cyt increase (from 0.51±0.02 to 0.13±0.03 au, n=33, P<0.01) (Fig. 1 b and e). A different type of Cl⁻ channel blocker, 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid (DIDS)–one of the stilbene derivatives that is structurally unrelated to fenamates–also caused a significant inhibition of the angiotensin II-induced [Ca²⁺]_cyt increase (from 0.43±0.04 to 0.06±0.01 au, n=18, P<0.01) (Fig. 1c and f). These data indicated that the function of Cl_Ca channels is involved in regulating ROCE in human PASMCs; inhibition of Cl_Ca channels significantly and reversibly attenuates the agonist-mediated Ca²⁺ entry.

Figure 1:

Attenuation of ROCE by Cl_Ca channel blockers in human PASMCs. Angiotensin II (AngII, 100 nM) was used to induce ROCE in human PASMCs. (a–c) Representative traces showing angiotensin II-induced [Ca²⁺]_cyt increases in human PASMCs before, during, and after application of 100 μM niflumic acid (NFA; a), flufenamic acid (FFA; b), and DIDS (c). Blockage of Cl_Ca channels reduces angiotensin II-induced [Ca²⁺]_cyt elevation in human PASMCs. (d–f) Summarized data showing the reversible inhibitory effects of niflumic acid (d), flufenamic acid (e), and DIDS (f) on angiotensin II-induced [Ca²⁺]_cyt rises in human PASMCs. Statistical signifcance (versus control) is indicated as **P<0.01.

Figure 2:

Effects of Ca²⁺ channel blockers on ROCE in human PASMCs. Angiotensin II (AngII, 100 nM) was used to induce ROCE in human PASMCs. (a–c) Representative traces showing angiotensin II-induced [Ca²⁺]_cyt rises in human PASMCs before, during, and after application of 50 μM SKF-96365 (SKF, an inhibitor of nonselective cation channels; a), 100 μM 2-APB (which blocks IP₃Rs and also non-selective cation channels; b), and 10 μM diltiazem (a VDCC blocker; c). (d–f) Summarized data showing effects of SKF-96365 (d), 2-APB (e), and diltiazem (f) on angiotensin II-induced [Ca²⁺]_cyt increase in human PASMCs. Statistical significance (versus control) is indicated as **P<0.01.

Effects of Ca²⁺ channel blockers on ROCE in human PASMCs

To elucidate the Ca²⁺ signal pathway for angiotensin II-induced ROCE, effects of the inhibitors for several different types of Ca²⁺ channels were examined in human PASMCs. The angiotensin II-mediated increase in [Ca²⁺]_cyt was reduced by treatment with 50 μM SKF-96365, an inhibitor of non-selective cation channels (from 0.59±0.05 to 0.28±0.04 au, n=13, P<0.01) (Fig. 2 a and d). The application of 100 μM 2-aminoethoxydiphenylborate (2-APB), which blocks IP₃Rs and also non-selective cation channels, abolished the angiotensin II-induced increase in [Ca²⁺]_cyt (from 0.46±0.03 to 0.08±0.01 au, n=22, P<0.01) (Fig. 2 b and e). Blockage of VDCC with 10 μM diltiazem, however, had a trend to inhibit the angiotensin II-induced [Ca²⁺]_cyt increase (from 0.45±0.02 to 0.36±0.03 au, n=35, P>0.05 by Scheffé's test, but P<0.01 by Student's t-test) (Fig. 2 c and f). These pharmacological data indicate that the angiotensin II-induced [Ca²⁺]_cyt increase was mainly caused by Ca²⁺ release from the SR through IP₃R followed by Ca²⁺ influx via non-selective cation channels in human PASMCs. Ca²⁺ influx through the diltiazem-sensitive L-type VDCCs slightly contributes to the angiotensin II-induced rise of [Ca²⁺]_cyt in human PASMCs.

Inhibitory effect of Cl_Ca channel blockers on SOCE in human PASMCs

In the next set of experiments, we examined the effect of Cl_Ca channel blockers on SOCE in human PASMCs (Fig. 3). SOCE was induced by passive depletion of Ca²⁺ from the SR with 10 μM cyclopiazonic acid (CPA), a blocker of SERCA. In the absence of extracellular Ca²⁺, application of CPA induced a transient increase in [Ca²⁺]_cyt that was due predominantly to Ca²⁺ leakage from the SR to the cytosol. Restoration of extracellular Ca²⁺ after approximately 10 min. treatment with CPA caused another increase in [Ca²⁺]_cyt that was apparently due to Ca²⁺ influx through store-operated cation (or Ca²⁺) channels or SOCE.

Figure 3:

Attenuation of SOCE by Cl_Ca channel blocker in human PASMCs. SOCE was induced by passive depletion of Ca²⁺ from the SR with 10 µM CPA in human PASMCs. (a) Typical trace of CPA-induced Ca²⁺ release and SOCE in the absence (vehicle, 0.1% DMSO) and presence of 100 µM niflumic acid (NFA) in a human PASMC. Blockage of Cl_Ca channels caused a reduction of SOCE in human PASMCs. (b–d) Summarized data showing effects of niflumic acid on the resting [Ca²⁺]_cyt (b), the rise speed of SOCE (c), the transient and plateau amplitudes of CPA-induced SOCE (d) in human PASMCs. Statistical signifcance versus vehicle control is indicated as *P<0.05 or **P<0.01.

As shown in Figure 3, there were no significant differences in the resting [Ca²⁺]_cyt (0.59±0.02 versus 0.62±0.02 au, n=55, P=0.25) and the amplitude of the increase in [Ca²⁺]_cyt due to CPA-induced Ca²⁺ leakage from the SR to the cytosol when cells were treated with 100 µM niflumic acid or vehicle (0.1% DMSO) (Fig. 3 a and b). The transient and plateau phases of CPA-induced increases in [Ca²⁺]_cyt due to SOCE, as well as the amplitude and “rise-speed” of SOCE were all significantly decreased by 100 µM niflumic acid. The rise-speed of SOCE in the presence of niflumic acid (0.18±0.01 ratio/s, n=55) was significantly slower than that in the absence (0.36±0.04 ratio/s, P<0.01 (Fig. 3c). In addition, application of niflumic acid significantly reduced the amplitude of the transient (from 0.42±0.02 to 0.31±0.02 au, n=55; P<0.01) and plateau (from 0.15±0.01 to 0.10±0.01 au, n=55; P=0.02) phases of SOCE (Fig. 3a and d). Treatment of the cells with 100 µM flufenamic acid also significantly decreased the amplitude of the transient and plateau phases of CPA-induced SOCE in human PASMCs (n=34). These data clearly suggest that the activity of Cl_Ca channels is involved in regulating SOCE in human PASMCs.

Effects of Ca²⁺ channel blockers on SOCE in human PASMCs

To functionally define the Ca²⁺ channels responsible for CPA-mediated SOCE, we examined the effects of different Ca²⁺ channel blockers on SOCE in human PASMCs. The transient component of CPA-induced SOCE was significantly reduced by 50 µM SKF-96365 (0.21±0.01 au, n=51, versus vehicle control, 0.37±0.01 au, n=58; P<0.01) (Fig. 4 a, b and e) and 100 μM 2-APB (0.10±0.01 au, n=46, P<0.01) (Fig. 4 c and e). Application of 10 μM diltiazem slightly (but significantly) affected the transient component of SOCE (from 0.37±0.01 to 0.32±0.01 au, n=42, P<0.01), but had no effect on the plateau phase of SOCE (from 0.16±0.01 au, n=58, to 0.14±0.01 au, n=42, P=0.22) (Fig. 4 a, d and e). Similar to their effects on the transient phase of SOCE, 50 µM SKF-96365 (from 0.16±0.01, n=58, to 0.06±0.01 au, n=51; P<0.01) (Fig. 4a, b and e) or 100 μM 2-APB (to 0.05±0.01 au, n=46, P<0.01) (Fig. 4c and e) also significantly reduced the plateau phase of CPA-induced SOCE. These pharmacological data indicate that the Ca²⁺ signaling pathway for CPA-induced SOCE was mainly dependent on Ca²⁺ influx through non-selective cation channels in human PASMCs. The activity of VDCCs might be, in part, involved in the Ca²⁺ influx pathway in human PASMCs.

Figure 4:

Effects of Ca²⁺ channel blockers on SOCE in human PASMCs. SOCE was induced by passive depletion of Ca²⁺ from the SR with 10 µM CPA in human PASMCs. (a–d) Typical traces showing CPA-induced Ca²⁺ release and SOCE in the absence (vehicle, 0.1% DMSO; a) and presence of 50 µM SKF-96365 (SKF, a blocker for non-selective cation channels; b), 100 µM 2-APB (a blocker of IP₃Rs and non-selective cation channels; c), and 10 µM diltiazem (an inhibitor of VDCCs; d) in human PASMCs. (e) Summarized data showing effects of Ca²⁺ channel blockers on the transient and plateau amplitudes of CPA-induced SOCE in human PASMCs. The number of cells examined is given in parentheses. Statistical significance versus vehicle control is indicated as **P<0.01.

Whole-cell Cl_Ca currents in human PASMCs

Electrophysiological and pharmacological properties of Cl_Ca currents in human PASMCs were analyzed by whole-cell patch-clamp configuration using a pipette (intracellular) solution containing 120 mM Cs⁺, 20 mM TEA (pCa=6.0) and a bath (extracellular) solution containing 10 mM TEA and 5 mM 4-AP. The mean cell-capacitance was 9.0±1.2 pF (n=14). Depolarizing pulses (500 ms) were applied from a holding potential of −60 mV to a series of test potentials ranging from −80 to +100 mV by 20-mV increments every 15 sec. Outward currents were elicited by depolarization from the holding potential to the positive potentials above 0 mV, and the averaged current density at +100 mV was 86±7 pA/pF (n=14) (Fig. 5 a and b). The reversal potential of the whole-cell currents was −3.4±1.3 mV (n=14) (Fig. 5b), which is close to the theoretical (or calculated) equilibrium potential of Cl⁻ (+0.1 mV). In addition, the reversal potential was shifted positively (to the right) by approximately 30 mV (positive shift by 36 mV in theory) by changing the extracellular Cl⁻ concentration from 153.8 to 36.8 mM (data not shown). Importantly, we were able to detect inward “tail” currents when cells were repolarized to the holding potential (Fig. 5a), which is an important characteristic of Cl_Ca currents. Furthermore, we analyzed the tail currents and the current-voltage relationship using the pulse protocol as follows: depolarizing pre-pulses were applied from a holding potential of −60 to +100 mV for 100 ms and subsequently test pulses were applied between −40 to +40 mV by 10-mV increments for 500 ms every 15 sec. (Fig. 5c). The current-voltage relationship revealed that the reversal potential of the tail currents (1.9±0.9 mV, n=4; Fig. 5d) was also very close to the theoretical (or calculated) equilibrium potential of Cl⁻.

Figure 5:

Whole-cell Cl_Ca currents in human PASMCs. Cl_Ca currents were measured using a pipette solution containing 120 mM Cs⁺, 20 mM TEA and pCa 6.0, and a bath solution containing 10 mM TEA and 5 mM 4-AP in human PASMCs. (a) Representative outward currents (black arrowhead), elicited by depolarization from a holding potential of −60 mV to a series of test potentials (−80 to +100 mV) for 500 ms every 15 sec. and inward tail currents (gray arrowhead), induced by repolarization to −60 mV in a human PASMC. (b) I-V relationship at peak amplitude during depolarization (black arrowhead in “a”). The current reverses at about 0 mV, the theoretical equilibrium potential of Cl⁻. (c) Representative tail currents (gray arrowhead) at a series of test potentials (−40 to +40 mV) for 500 ms after depolarization from a holding potential of −60 to +100 mV for 100 ms every 15 sec. in a human PASMC. (d) I-V relationship of tail currents (gray arrowhead in “c”). The reversal potential is close to 0 m V.

Application of 100 µM niflumic acid significantly attenuated both the outward Cl_Ca current and the inward tail current in human PASMCs (Fig. 6). Niflumic acid decreased the outward currents elicited by depolarization from a holding potential of −60 to +60 mV (for 500 ms every 15 s) (from 37.4±5.3 to 16.5±1.2 pA/pF, n=3; P=0.046). The inward tail currents were also inhibited by the pretreatment with niflumic acid (−5.6±1.3 pA/pF, n=3, versus control of −22.2±4.7 pA/pF, P=0.040). These electrophysiological data indicate that Cl_Ca channels sensitive to niflumic acid are functionally expressed in human PASMCs.

Figure 6:

Inhibition of Cl_Ca currents by niflumic acid in human PASMCs. Effect of niflumic acid on whole-cell Cl_Ca currents was examined in human PASMCs. (a) Representative outward currents (black arrowhead), elicited by depolarization from a holding potential of −60 to +60 mV, and inward tail currents (gray arrowhead), induced by repolarization to −60 mV in the absence (black line) and presence (gray line) of 100 µM niflumic acid (NFA) in a human PASMC. (b) Summarized data showing the effect of niflumic acid on outward (black arrowhead in “a”) and tail (gray arrowhead in “a”) currents in human PASMCs. The number of cells examined is given in parentheses. Statistical significance versus control is indicated as *P<0.05.

Expression of TMEM16A in human PASMCs

The molecular basis of Cl_Ca channels in human PASMCs was identified by an immunocytochemical approach using two specific primary antibodies of TMEM16A (ab53213 and ab53212 from Abcam), a potential protein candidate for Cl_Ca channels. Immunocytochemical experiments (Fig. 7) revealed that specific fluorescent signals of TMEM16A protein were localized in the cell membrane. Qualitatively, the same images were obtained from 3 separate sets of experiments. This result indicates that the activity of Cl_Ca channels in human PASMCs is potentially due to channels formed by TMEM16A.

Figure 7:

Expression of TMEM16A in human PASMCs. Immunocytochemical analysis of TMEM16A, a potential candidate for the Cl_Ca channel subunit, was performed in human PASMCs using two specific primary antibodies (ab53213 and ab53212 from Abcam). Alexa Fluor 488 and DAPI were used as a secondary antibody and a nuclear marker, respectively. Specific signals of TMEM16A protein were detected on the plasma membranes of human PASMCs. Similar immunocytochemical images were obtained from 3 sets of independent experiments.

DISCUSSION

In vascular smooth muscle cells, Cl_Ca channels are present for diverse physiological and pathological functions. In this study, we showed that the blockage of Cl_Ca channels using pharmacological tools markedly attenuated both ROCE and SOCE in human PASMCs. Our electrophysiological and immunocytochemical data also indicated that the activity of Cl_Ca channels functionally expressed in human PASMCs was due potentially to channels formed by TMEM16A proteins.

Intracellular free Ca²⁺ plays an important role in the regulation of contraction, proliferation, and migration of PASMCs. An increase in [Ca²⁺]_cyt in PASMCs is a major trigger for pulmonary vasoconstriction and an important stimulus for PASMC proliferation that leads to pulmonary vascular remodeling under pathological conditions. Elevation of [Ca²⁺]_cyt in PASMCs results from Ca²⁺ release from intracellular stores, such as the SR, and Ca²⁺ influx through plasmalemmal Ca²⁺ channels, such as ROC channels, SOC channels, and VDCCs.^[1,2]

Angiotensin II is a vasoconstrictor that is commonly used for eliciting agonist-induced [Ca²⁺]_cyt rises in PASMCs and other vascular smooth muscle cells.^[21,22] In this study, we used angiotensin II to induce ROCE because, at the concentration of 100 nM, it caused an increase in [Ca²⁺]_cyt in a large number of human PASMCs (>70%). The angiotensin II-mediated increase in [Ca²⁺]_cyt via ROCE was markedly reduced by two different types of Cl_Ca channel inhibitors, fenamates (niflumic acid and flufenamic acid) and one of the stilbene derivatives (DIDS). Both niflumic acid and flufenamic acid are well known fenamates that are most frequently used as Cl_Ca channel blockers in electrophysiological and pharmacological studies. However, these compounds have been reported to also act on other types of ion channels such as non-selective cation channels,^[23] large-conductance Ca²⁺-activated K⁺ channels,^[24] and transient receptor potential canonical subfamily (TRPC) channels.^[25] Therefore, to confirm whether or not the inhibitory effects of niflumic acid and flufenamic acid on the angiotensin II-evoked increase in [Ca²⁺]_cyt in human PASMCs were mediated by the blockage of Cl_Ca channels, we analyzed the effects of another type of Cl_Ca channel blocker, DIDS, a stilbene derivative that is structurally unrelated to fenamates, on the angiotensin II-induced [Ca²⁺]_cyt increase. Similar to niflumic acid and flufenamic acid, DIDS also significantly suppressed the angiotensin II-induced [Ca²⁺]_cyt increase, although it might have interfered with the fura-2 fluorescence due to its faint yellow colored solution at a concentration of 100 µM. These results, by using two different types of Cl_Ca channel blockers, strongly suggest that the function of Cl_Ca channels is involved in regulating ROCE in human PASMCs.

SOCE is essential for maintaining a high level of [Ca²⁺]_cyt and for refilling intracellular Ca²⁺ stores (i.e., SR) in smooth muscle cells.^[1,10–12] High levels of [Ca²⁺]_cyt and sufficient levels of Ca²⁺ in the SR are required for proliferation of vascular smooth muscle cells.^[1,10] SOCE is enhanced while SOC channels are upregulated during PASMC proliferation to increase Ca²⁺ influx and provide sufficient Ca²⁺ for activation of the intracellular mechanisms responsible for cell proliferation and growth.^[9,13,14] In the present study, we demonstrated that the blockage of Cl_Ca channels by niflumic acid and flufenamic acid reduced both the transient and plateau components of SOCE as well as the rise speed of SOCE in human PASMCs. These data indicate that the function of Cl_Ca channels is also involved in regulating SOCE in human PASMCs (in addition to the effect on ROCE). Suppression of SOCE by blockage of Cl_Ca channels is thought to cause reduced PASMC proliferation, which may be a novel strategy for preventing the abnormal proliferation under pathological conditions. TRPC channels have been demonstrated to be involved in agonist- or growth factor-mediated Ca²⁺ entry in PASMCs,^[1,10,26] while functional coupling of stromal interaction molecule (STIM) proteins (STIM1 and STIM2) with TRPC and/or Orai channels have recently been suggested as a novel candidate for SOC channel subunits in PASMCs.^[27–29] TRPC channel genes are thought to encode pore-forming subunits that compose ROC^[30–32] and SOC^[33–35] channels in many cell types of vascular smooth muscles including PASMCs.^{[9,13,14,36–38]} Ca²⁺ entry via ROC and SOC channels is modulated by second messengers, phosphorylation of signal transduction proteins, and transcription factors.^[2,10,39] The protein expression levels of TRPC, STIM and Orai are changed under pathological conditions such as in pulmonary arterial hypertension.^[1,10,39]

Smooth muscle cells contain a high concentration of Cl⁻ in the intracellular space, which is considerably different from other cell types, such as neurons, cardiomyocytes, and skeletal muscle myocytes.^[17] Therefore, increases in Cl⁻ conductance across the plasma membrane (e.g., as a result of activation of Cl_Ca channels when [Ca²⁺]_cyt is increased) lead to Cl⁻ efflux and inward currents, which consequently causes membrane depolarization, enhanced Ca²⁺ influx through VDCCs, increased [Ca²⁺]_cyt, and vasoconstriction.^[15,16] In the present study, electrophysiological data indicated that Cl_Ca channels were functionally expressed in human PASMCs and the Cl⁻ currents through Cl_Ca channels were sensitive to niflumic acid. The electrophysiological properties (e.g., the time-dependent outward current during membrane depolarization, the inward tail current during repolarization, the outward rectification, and the shift of reversal potential based on the change in extracellular Cl⁻ concentration) and pharmacological properties (e.g., the dependency on intracellular Ca²⁺ concentration and the sensitivity to niflumic acid) of whole-cell Cl_Ca currents obtained from human PASMCs were consistent with the same properties reported previously in PASMCs from rabbits^[40] and rats.^[41,42] The [Ca²⁺]_cyt increase mediated by ROCE and SOCE also activates the Cl_Ca channels, resulting in membrane depolarization followed by additional Ca²⁺ influx through VDCCs. Slight decreases in ROCE and SOCE by diltiazem, a VDCC blocker, suggested that VDCCs only partly contributed to the regulation of ROCE and SOCE, although the Ca²⁺ influx pathway was mainly due to non-selective Ca²⁺ channels sensitive to SKF-96365 and 2-APB in human PASMCs.

Cl_Ca channels play important roles in diverse functions in vascular smooth muscle cells. In spite of its physiological and pathological significances, the molecular architecture of Cl_Ca channels in vascular smooth muscle cells has not been clearly demonstrated. More recently, the TMEM16 family, consisting of 10 genes in mammals, has been found as a novel candidate for Cl_Ca channel subunits.^[18–20,43] Heterologous expression of TMEM16A has been shown to generate Cl⁻ currents sensitive to intracellular Ca²⁺ and with the degree of outward rectification, ion selectivity, and pharmacological profile^[18–20] similar to the activity of native Cl_Ca channels observed in many tissues containing interstitial cells of Cajal in gastrointestinal muscles,^[44–46] airway epithelial cells,^[47,48] as well as vascular smooth muscle cells.^[42,49] The distribution pattern of TMEM16A in interstitial cells of Cajal in gastrointestinal muscles,^[44–46,50] airway epithelial cells,^[47,48] and vascular smooth muscle cells^[49] implies the functional expression of Cl_Ca conductance. In this study, TMEM16A protein was localized in the plasma membrane of human PASMCs, indicating that the activity of the Cl_Ca channel in human PASMCs was, at least in part, due to channels formed by TMEM16A. It has been reported that the TMEM16A gene also has some splice variants^{[18,42,49,51]} and TMEM16B, a closely related analogue, also can generate Cl⁻ currents activated by Ca²⁺.^[19,52–54] It is unclear whether TMEM16B is another subunit that forms Cl_Ca channels in human PASMCs.

Pulmonary arterial hypertension is a fatal and progressive disease characterized pathologically by severe pulmonary vascular remodeling. A central aspect of pulmonary vascular remodeling is adventitial, medial, and intimal hypertrophy caused by excessive proliferation of fibroblasts and myofibroblasts in the adventitia, PASMCs in the media and endothelial cells in the intima. The concentric pulmonary vascular wall remodeling or thickened arterial and arteriole wall, narrows the intra-arterial lumen, increases pulmonary vascular resistance and ultimately causes pulmonary hypertension.^[2,39] Since SOC and ROC channels are upregulated in PASMC isolated from patients with idiopathic pulmonary arterial hypertension (IPAH) and from animals with hypoxia-mediated pulmonary hypertension, Ca²⁺ entry through these upregulated cation channels may play an important pathogenic role in the initiation and progression of pulmonary vascular remodeling under the pathological conditions.?^{[1,10,14,26,28,37]} It remains unclear, however, whether the activity of Cl_Ca channels is also involved in the sustained pulmonary vasoconstriction and excessive pulmonary vascular remodeling in patients with IPAH and animals with hypoxia-induced pulmonary hypertension. Based on the observations from this study, the attenuation of SOCE and ROCE by Cl_Ca channel blockers (e.g., niflumic acid, flufenamic acid, and DIDS) may serve as a potential therapeutic approach for pulmonary vascular disease. Although it is suggested that Cl⁻ channels are involved in SOCE and proliferation in PASMCs,^[55,56] further experiments are necessary to elucidate the mechanism underlying the regulation of ROCE and SOCE by Cl_Ca channels in human PASMCs.

Footnotes

Source of Support: This work was supported, in part, by grants from the National Heart, Lung, and Blood Institute of the National Institutes of Health (HL066012 and HL098053 to JX-JY),

Conflict of Interest: None declared.

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Activity of Ca 2+ -Activated Cl − Channels Contributes to Regulating Receptor- and Store-Operated Ca 2+ Entry in Human Pulmonary Artery Smooth Muscle Cells

Abstract

Keywords

INTRODUCTION

MATERIALS AND METHODS

Cell culture

[Ca2+]cyt measurement

Electrophysiological recording

Immunocytochemical staining

Drugs

Statistical analysis

RESULTS

Inhibition of agonist-induced Ca2+ influx or ROCE by ClCa channel blockers in human PASMCs

Effects of Ca2+ channel blockers on ROCE in human PASMCs

Inhibitory effect of ClCa channel blockers on SOCE in human PASMCs

Effects of Ca2+ channel blockers on SOCE in human PASMCs

Whole-cell ClCa currents in human PASMCs

Expression of TMEM16A in human PASMCs

DISCUSSION

Footnotes

References

[Ca²⁺]_cyt measurement

Inhibition of agonist-induced Ca²⁺ influx or ROCE by Cl_Ca channel blockers in human PASMCs

Effects of Ca²⁺ channel blockers on ROCE in human PASMCs

Inhibitory effect of Cl_Ca channel blockers on SOCE in human PASMCs

Effects of Ca²⁺ channel blockers on SOCE in human PASMCs

Whole-cell Cl_Ca currents in human PASMCs