- Original Paper
- Open Access
Insulin is involved in transcriptional regulation of NKCC and the CFTR Cl− channel through PI3K activation and ERK inactivation in renal epithelial cells
The Journal of Physiological Sciences volume 64, pages433–443(2014)
It is is well known that insulin stimulates glucose transport and epithelial Na+ channel (ENaC)-mediated Na+ reabsorption; however, the action of insulin on Cl− secretion is not fully understood. In this study, we investigated the action of insulin on Na+–K+–2Cl− cotransporter (NKCC)-mediated Cl− secretion in epithelial A6 cells. Interestingly, insulin treatment remarkably enhanced the forskolin-stimulated Cl− secretion associated with an increase in apical Cl− conductance by upregulating mRNA expression of both CFTR and NKCC, although insulin treatment alone had no effect on the basal Cl− secretion or apical Cl− conductance without forskolin application. We next elucidated a role of phosphoinositide 3-kinase (PI3K) in the insulin-induced enhancement of the Cl− secretion, since insulin actually activated PI3K, resulting in activation of Akt, a downstream molecule of PI3K. LY294002 (a PI3K inhibitor) reduced the Cl− secretion by suppressing mRNA expression of NKCC, whereas insulin still had a stimulatory action on mRNA expression of CFTR even in the presence of LY294002. On the other hand, we found that a MEK inhibitor (PD98059) further enhanced the insulin-stimulated CFTR mRNA expression and the Cl− secretion in forskolin-stimulated A6 cells and that insulin induced slight, transient activation of ERK followed by significant inactivation of ERK. These observations suggest that: (1) insulin respectively upregulates mRNA expression of NKCC and CFTR through activation of PI3K and inactivation of ERK; (2) insulin signals on mRNA expression of NKCC and CFTR are not enough to stimulate transepithelial Cl− secretion, but enhance the stimulatory action of cAMP on transepithelial Cl− secretion.
Transepithelial Cl− secretion from the interstitial space to the luminal one carries negative charges followed by movement of cations, such as Na+, K+ and H+ secretion [1–10]. The NaCl or KCl secretion, essentially driven by the transepithelial Cl− secretion, generates an osmotic gradient followed by water secretion. Thus, Cl− secretion is a crucial driving force for water secretion, forms an epithelial surface liquid protecting our bodies from bacterial and viral infections, and controls body fluid contents [1–4]. Therefore, understanding the regulatory mechanisms of transepithelial Cl− secretion is important for controlling the volume of fluid covering the epithelial surface and extracellular fluid (ECF). Transepithelial Cl− secretion is composed of two steps: a Cl− uptake step through active transporters such as Na+–K+–2Cl− cotransporter (NKCC) in the basolateral membrane and a Cl− releasing step through Cl− channels in the apical membrane [3, 4, 11]. To increase transepithelial Cl− secretion, at least one of the two steps should be stimulated [12–16]. Therefore, discovering factors regulating Cl− transporters and/or Cl− channels and clarifying the regulatory mechanism of transepithelial Cl− secretion are important for understanding the mechanisms of body fluid homeostasis.
Evidence accumulated by recent studies indicates physiological roles of transepithelial Cl− secretion, Cl− transporters and Cl− channels in water movement , cell differentiation [18–21], cell proliferation [22–26], and cell signaling and gene expression [27–32]. For instance, proliferation of poorly differentiated gastric cancer cells (MKN45) with higher expression of NKCC1 is faster than that of moderately differentiated gastric cancer cells (MKN28) with lower expression of NKCC1 . These observations suggest that expression levels of NKCC are correlated to the rate of proliferation and that growth factors possibly regulate cell growth via induction of NKCC1. In rat pheochromocytoma (PC12) cells, neuron growth factor (NGF) stimulates neurite elongation through increased NKCC expression, which is associated with intracellular Cl−-dependent tubulin polymerization . These observations suggest the importance of transepithelial Cl− secretion, Cl− transporters and Cl− channels for various cellular functions, not only for transepithelial ion transport.
Insulin is a well-known hormone that regulates glucose metabolism (blood sugar) through its binding to the insulin receptor in the target tissue. Insulin receptor is a transmembrane receptor tyrosine kinase, which is activated through autophosphorylation by ligand binding and transduces the signal into the intracellular space through a phosphoinositide 3-kinase (PI3K)-Akt-dependent cascade , which in turn coordinates cell growth , cell survival , glucose metabolism  and ion/glucose transport [34–44]. Insulin is also known to stimulate ENaC-mediated Na+ reabsorption in the distal nephron by increasing ENaC surface expression in the apical membrane [43, 45, 46]. The hypertension frequently observed in type 2 diabetes  is considered to be explained by hyperstimulation of ENaC-mediated Na+ reabsorption in hyperinsulinemia. Thus, abnormal regulation or hyperstimulation of ENaC-mediated Na+ reabsorption is considered to be strongly correlated to hypertension. However, the action of insulin on transepithelial Cl− secretion is still poorly understood. In this study, we investigated the transcriptional action of insulin on Cl− secretion and clarified that insulin-enhanced forskolin-stimulated Cl− secretion by upregulating mRNA expression of NKCC and CFTR and that translocation/activation of NKCC and CFTR might be independently regulated.
Materials and methods
Transwell-Clear permeable supports (PET membrane Transwell-Clear 6.5 and 24 mm) were obtained from Corning, Inc. (Lowell, MA, USA). NCTC-109 medium, benzamil, NPPB, insulin and forskolin were purchased from Sigma (St Louis, MO, USA). LY294002 and PD98059 were obtained from Calbiochem (San Diego, CA, USA).
The isotonic test solution contained 120 mM NaCl, 3.5 mM KCl, 1 mM CaCl2, 1 mM MgCl2, 5 mM glucose and 10 mM N-2-hydroxy-ethylpiperazine-N′-2-ethanesulfonic acid (HEPES) adjusted to pH 7.4.
Renal epithelial A6 cells derived from Xenopus laevis [48–50] were purchased from the American Type Culture Collection (ATCC). A6 cells (passage 73–84) were cultured as previously described [11, 51]. Namely, A6 cells (passage 73–84) were grown on plastic flasks at 27 °C in a humidified incubator with 1.0 % CO2 in air in a culture medium that contained 75 % (v/v) NCTC-109, 15 % (v/v) distilled water and 10 % (v/v) fetal bovine serum. For preparation of total RNA and cell lysate, A6 cells were cultured for 13–14 days on 24-mm Transwell-Clear permeable supports. For measurement of short-circuit current (Isc), A6 cells were cultured for 13–14 days on 6.5-mm Transwell-Clear permeable supports.
Measurement of the short-circuit current
Isc was measured as described previously [11, 51]. Monolayers of A6 cells subcultured on Transwell-Clear filter cups were transferred to a modified Ussing chamber (Jim’s Instrument Manufacturing, Iowa City, IA, USA). Transepithelial potential (PD) was continuously measured by a high-impedance millivoltmeter that could function as a voltage clamp with automatic fluid resistance compensation (VCC-600, Physiologic Instruments, San Diego, CA, USA) with a pair of calomel electrodes that were bridged to the modified Ussing chamber by a pair of polyethylene tubes filled with a solution of 2 % (w/v) agarose in a 2-M KCl solution. Isc was measured by the amplifier, VCC-600, with a pair of silver–silver chloride electrodes that were bridged to the modified Ussing chamber by a pair of polyethylene tubes filled with a solution of 2 % (w/v) agarose in a 2-M NaCl solution. When the Isc was measured, the PD was clamped to 0 mV for 1 s by the amplifier. Under a steady condition, the Isc was stable and did not change even if the transepithelial voltage was clamped to 0 mV for 1 min. In a non-steady state, the value of Isc measured at 1 s after clamping the PD to 0 mV is shown as Isc in the present study. A positive current represents a net flow of anions from the basolateral to the apical solution. To detect the transepithelial Cl− secretion, we added 100 μM NPPB (a non-selective Cl− channel blocker [52–54]) to the apical solution and measured an NPPB-sensitive Isc by calculating the difference between the Isc just before and 30 min after application of 100 μM NPPB. We show this difference of Isc as an NPPB-sensitive Isc.
Measurement of transepithelial conductance (Gt)
We measured Gt using the same method as that previously reported in our study  using a high-impedance millivoltmeter (VCC-600). Namely, we applied an 1-μA constant current pulse every 10 s for 0.5 s to the A6 monolayer under open-circuit conditions, enabling us to evaluate the Gt by measuring the change in the PD (ΔPD) caused by the 1 μA constant-current pulse using Ohm’s law (Gt = 1 μA/ΔPD mV). To detect the apical Cl− conductance, we added 100 μM NPPB (a non-selective Cl− channel blocker [52–54]) to the apical solution and measured an NPPB-sensitive conductance by calculating the difference between the Gt just before and 30 min after application of 100 μM NPPB. We show this difference of Gt as an NPPB-sensitive conductance (i.e., the apical Cl− conductance), since the apical Cl− conductance is much smaller than the basolateral Cl− conductance . We have already confirmed that the apical Cl− conductance is diminished by apical application of 100 μM NPPB, but not the basolateral Cl− conductance [55, 56]. Thus, we indicate that the NPPB-sensitive conductance can be used as the apical Cl− conductance [55, 56].
The confluent A6 monolayers grown on Transwell-Clear permeable supports were lysed by lysis buffer (50 mM HEPES, 120 mM NaCl, 1.5 mM MgCl2, 1 mM EGTA, 10 % glycerol, 1 % Triton X-100, 100 mM NaF, 10 mM pyrophosphate, 250 μg/ml leupeptin, 0.1 mM phenyl methylsulfonyl fluoride, 100 Kallokein inactivator units/ml aprotinin, pH 7.4) after various experimental treatments. Then, cells were homogenized by sonication and centrifuged at 21,880 g for 10 min at 4 °C to remove insoluble debris. The cell lysates containing 50 μg protein were boiled in SDS sample buffer [60 mM Tris-HCl, 2 % (w/v) SDS, 5 % (v/v) glycerol, pH 6.8] and then subjected to SDS-polyacrylamide gel electrophoresis (SDS-PAGE). After electrophoresis, proteins were transferred to nitrocellulose membranes. Nonspecific binding was blocked by incubation in 5 % (w/v) nonfat milk in Tris-buffered saline (TBS) containing 0.1 % Tween 20 (TBST) at room temperature for 60 min. Membranes were blotted with anti-phospho-ERK (Thr202/Tyr204), anti-phospho-Akt (Ser473) and anti-β-tubulin antibodies (Cell Signaling Technology, Beverly, MA, USA) in 5 % BSA in TBST at 4 °C overnight. The membranes were then washed with TBST and incubated for 60 min at room temperature with horseradish peroxidase (HRP)-conjugated anti-rabbit IgG (Cell Signaling Technology, Denver, MA, USA) in 5 % (w/v) non-fat milk in TBST. After washing with TBST, the blots were detected with ECL prime chemiluminescent reagent (GE Healthcare Bio-Sciences Corp., Piscataway, NJ, USA). Each blot presented was performed at least three times.
Quantitative real-time PCR
To compare relative amounts of mRNA for NKCC1 and the CFTR Cl− channel in A6 monolayers treated under different conditions, we performed quantitative real-time PCR. Total RNA was extracted from A6 monolayers using an RNeasy kit (QIAGEN, Tokyo, Japan) with DNase digestion according to the manufacture’s protocol. Reverse transcription (RT) was performed on 1 μg total RNA, calculated from absorbance measured at 260 nm, using a High Capacity Coda transcription kit (Applied Biosystems, Rotkreuz, Switzerland) according to the manufacturer’s protocol. Primers (SIGMA Genosis) and TaqMan probes (Applied Biosystems, Rotkreuz, Switzerland) unique for each Xenopus NKCC, Xenopus CFTR Cl− channel or Xenopus Β-actin were the following: xNKCC forward 5′-TGCCTCCCTTGCCAAGTCT-3′, reverse 5′-CGAGTGACACCCACATGTTGTA-3′, TaqMan probe 5′-AGGATGGCGTCCCGCCTTCAGATA-3′, xCFTR forward 5′-ATGCTATTCTACATGCCCCAATG-3′, reverse 5′-TCCAATATAGCTGTATCCTTTGAAAATC-3′, TaqMan probe 5′-ACCTTCAATACAATGAGAGCTGGTCGGATACTTAA-3′, xβ-actin forward 5′-GATGCTCCCCGTGCTGTTT-3′, reverse 5′-TTCCAACCATGACACCCTGA-3′, TaqMan probe 5′-CCCATCTATTGTGGGTCGCCCAAGA-3′. Quantitative real-time PCR with TaqMan probes using the ABI 7300 real-time PCR system was performed according to the manufacturer’s protocol. Diluted RT samples (100 ng total RNA) were amplified in a final volume of 25 μl. Primers were used at a concentration of 800 nM and probes at a concentration of 200 nM. β-actin were used as an internal control. The thermal cycling conditions were as follows: 50 °C for 2 min and 95 °C for 10 min, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min. Relative amounts of NKCC and CFTR Cl− channel mRNA were determined by normalization with β-actin mRNA expression.
All experiments for electrophysiological and other measurements were performed at 24–25 °C unless otherwise indicated.
All data are presented as mean ± standard error of the mean (SEM). Where SEM bars are not visible, they are smaller than the symbol. Student’s t test and ANOVA were used for statistical analysis as appropriate, and p < 0.05 was considered significant.
Enhancement of forskolin-stimulated Cl− secretion by insulin pretreatment
The Cl− secretion is generally composed of two steps: (1) the step of Cl− uptake via the Na+–K+–2Cl− cotransporter 1 (NKCC1) at the basolateral membrane and (2) the step of Cl− release via the cystic fibrosis transmembrane conductance regulator (CFTR) Cl− channel at the apical membrane [11, 57]. Elevation of cytosolic cAMP by bilateral application of 10 μM forskolin stimulated the Cl− secretion through activation of both the apical Cl− channels and basolateral NKCC1 in A6 cells. In this study, transepithelial Cl− secretion and apical Cl− channel activities are respectively determined as NPPB (a Cl− channel blocker)-sensitive Isc and NPPB-sensitive conductance (Gt) by addition of 100 μM NPPB to the apical solution. In all of the experiments, to isolate the Cl− secretion from the Na+ absorption, we added 10 μM benzamil, which is a specific inhibitor of ENaC and completely blocks the ENaC at the concentration (10 μM) [30, 58], to the apical solution 10 min before application of forskolin. In this study, we measured NPPB-sensitive Isc and Gt after pretreatment of A6 monolayers with insulin, which shows its maximum effect on ion transport within 100 nM–1 μM [59, 60]. Thus, we applied 1 μM of insulin to obtain its maximum effect in the present study. We preincubated A6 cells with or without 1 μM insulin in the absence or presence of inhibitors in the culture medium for various time periods, then washed out insulin and inhibitors, and set the pretreated A6 monolayers to the modified Ussing chamber in 120 mM NaCl solution without any insulin and inhibitors. Then, we stimulated the A6 monolayers in 120 mM NaCl solution with 10 μM forskolin 10 min after addition of 10 μM benzamil. Finally, NPPB of 100 μM was added to the apical solution 60 min after application of forskolin, and the differences in Isc and Gt between just before and 30 min after addition of NPPB were measured as NPPB-sensitive Isc and Gt.
Acute (0–60 min) or chronic (2–24 h) application of insulin to the basolateral solution had no effect on basal Cl− secretion detected as NPPB-sensitive Isc in A6 cells (data not shown). To clarify the action of insulin on cAMP-stimulated Cl− secretion, we pretreated A6 cells with 1 μM insulin for 0, 1, 3, 6 and 24 h in the culture medium and washed out the insulin. Just after washing out the insulin, 10 μM of forskolin was applied to the apical and basolateral solutions for elevation of cytosolic cAMP concentration. Then, we measured NPPB-sensitive Isc and Gt by adding 100 μM NPPB 60 min after application of forskolin in the absence of insulin. Pretreatment of monolayered A6 cells with 1 μM insulin for more than 3 h markedly enhanced the forskolin-stimulated Cl− secretion (NPPB-sensitive Isc) by increasing apical Cl− channel activities (conductances) detected as NPPB-sensitive Gt (Fig. 1). Pretreatment with insulin for 6 h had similar effects to that for 24 h, which showed the maximum effects on the enhancement of forskolin-stimulated Cl− secretion (NPPB-sensitive Isc) and conductance (NPPB-sensitive Gt) (Fig. 1). It is notable that application of insulin alone had no stimulatory action on Cl− secretion (NPPB-sensitive Isc) or conductance (NPPB-sensitive Gt) in the absence of forskolin. Namely, the NPPB-sensitive Isc was 0.30 ± 0.03 μA/cm2 (n = 7) in cells preincubated with insulin for 24 h, which was not significantly different from that without insulin (0.23 ± 0.03 μA/cm2 without insulin; n = 7): the NPPB-sensitive Gt was 22.04 ± 1.31 μA/cm2 (n = 7) in cells preincubated with insulin for 24 h, which was not significantly different from that without insulin (18.67 ± 1.38 μS/cm2 without insulin; n = 7).
Insulin enhanced the Cl− secretion through transcriptional regulation of NKCC and CFTR
Incubation with insulin for at least 3 h is required for enhancement of the Cl− secretion, suggesting that transcriptional regulation in NKCC and/or CFTR might be involved in the enhancement of the Cl− secretion. To elucidate this suggestion, we next examined the effect of insulin on mRNA expression of NKCC and CFTR by quantitative real-time PCR. Pretreatment of monolayered A6 cells with 1 μM insulin for 24 h remarkably increased mRNA expression of both NKCC and CFTR (Fig. 2). This result suggests that insulin enhanced forskolin-stimulated Cl− secretion by increasing mRNA expression of both NKCC and CFTR.
Involvement of PI3K in the transcriptional regulation of NKCC and CFTR
We next addressed the question of how insulin induces mRNA expression of NKCC and CFTR. As PI3K is a major signal molecule in the insulin cascade, we examined whether insulin activates PI3K in monolayered A6 cells by detecting Akt phosphorylation. Insulin increased phosphorylation of Akt at Ser473 (Fig. 3), which is known to be phosphorylated through a PI3K-dependent pathway. To clarify the involvement of PI3K in the insulin-induced mRNA expression of NKCC and CFTR, we examined the effects of LY294002 (a specific inhibitor of PI3K). Pretreatment with LY294002 markedly reduced mRNA expression of NKCC and CFTR in insulin-untreated and -treated A6 cells (Fig. 4a). The treatment with LY294002 blocked the stimulatory action of insulin on NKCC mRNA expression, but not CFTR mRNA expression (Fig. 4a). This observation suggests that insulin upregulates NKCC mRNA expression by mainly activating a PI3K-dependent pathway, but CFTR mRNA expression via a PI3K-independent pathway.
To further elucidate a PI3K-independent pathway for CFTR mRNA expression, we examined a possible role of ERK in CFTR mRNA expression by using PD98059 (a MEK inhibitor blocking ERK activation). Pretreatment of monolayered A6 cells with PD98059 did not affect NKCC mRNA expression, but further increased CFTR mRNA expression in insulin-treated A6 cells (Fig. 4b). These observations suggest that ERK would be a negative regulator for CFTR mRNA expression and that insulin might inactivate ERK, leading to an increase in CFTR mRNA expression through a PI3K-independent pathway. To confirm this presumption, we examined whether insulin inactivates ERK by detecting activated (phosphorylated) ERK with immunoblotting. Insulin induced slight, transient activation followed by a remarkable inactivation (dephosphorylation) of ERK (Fig. 5). Based on these results, we suggest that insulin increases CFTR mRNA expression via suppression of ERK in a PI3K-independent manner.
The regulatory mechanism of forskolin-stimulated Cl− secretion by insulin
In this study, we indicated that insulin enhanced the forskolin-stimulated Cl− secretion by increasing respectively mRNA expression of both NKCC and CFTR through PI3K activation and ERK inactivation. We next elucidated whether PI3K-dependent transcriptional regulation in NKCC and CFTR actually participates in the enhancement of forskolin-stimulated Cl− secretion by insulin in A6 cells. Pretreatment with LY294002 slightly decreased the forskolin-stimulated NPPB-sensitive Isc associated with a similar rate of reduction of NPPB-sensitive Gt in insulin-untreated A6 cells [(−) Insulin in Fig. 6a, b]. Likewise, LY294002 remarkably suppressed the insulin-induced enhancement of forskolin-stimulated NPBB-sensitive Isc associated with suppression of NPPB-sensitive Gt to a similar extent as Isc [(+) Insulin in Fig. 6a, b]. Consequently, most of the insulin-induced enhancement of forskolin-stimulated Cl− secretion and Cl− channel conductance (activity) was sensitive to LY294002, suggesting that insulin enhances the forskolin-stimulated Cl− secretion and Cl− channel conductance via a PI3K-dependent pathway (Fig. 6). On the contrary, pretreatment with PD98059 further increased the insulin-induced enhancement of forskolin-stimulated Cl− secretion accompanied by further elevation of apical Cl− channel conductance (activity) (Fig. 7), suggesting that complete inhibition of ERK forcibly caused by PD98059 further increased the insulin-pretreatment-stimulated Cl− secretion via further enhancement of CFTR expression in forskolin-stimulated cells.
cAMP-dependent regulation of NKCC and/or CFTR translocation
mRNA expression of NKCC and CFTR is upregulated by insulin; nevertheless, the basal Cl− secretion or apical Cl− channel conductance (activity) was not significantly increased. There are two possible explanations for these phenomena. One is that insulin induced too small increases in basal Cl− secretion and apical Cl− channel conductance (activity) to detect the increases. The other is that insulin signals alone are not enough to translocate proteins of NKCC and/or CFTR newly synthesized by insulin pretreatment to the plasma membrane for stimulation of Cl− secretion. To confirm this presumption, we examined the effects of brefeldin A (BFA; an inhibitor of protein translocation from ER to Golgi) on the insulin-induced enhancement of Cl− secretion and apical Cl− channel conductance (activity) in forskolin-stimulated cells. After pretreatment with insulin for 5 h, we further pretreated A6 cells with both insulin and BFA (5 μg/ml) for 1 h. Then, we measured Cl− secretion and apical Cl− channel conductance (activity) in forskolin-stimulated cells in the absence or presence of BFA. BFA abolished the stimulatory action of insulin on Cl− secretion (Fig. 8a) and apical Cl− channel conductance (activity: Fig. 8b) in forskolin-stimulated cells.
In this study, we elucidate that insulin enhanced forskolin-stimulated Cl− secretion and apical Cl− channel conductance (activity) by respectively upregulating mRNA expression of NKCC and CFTR via activation of PI3K-Akt and inactivation of ERK in epithelial A6 cells. Previous studies indicated the action of growth factors including insulin on NKCC. Insulin activates NKCC in human fibroblast , 3T3-L1 fibroblast, adipocyte  and L6 cells  regulating cell volume and K+ uptake. IGF-1 (insulin-like growth factor-1) increases NKCC mRNA expression in pavement cells , while EGF (epidermal growth factor) and NGF increase NKCC protein expression in intestinal epithelial cells  and PC12 cells . In human skin fibroblasts, EGF-induced activation of NKCC is crucial for mitogenic signaling pathways . Thus, these studies indicate that growth factors regulate NKCC expression at transcriptional, translational and posttranslational levels in various types of cells. On the other hand, NKCC basically contributes to Cl− uptake from extracellular into intracellular space regulating the cell volume, intracellular Cl− concentration ([Cl−] i ) and transepithelial Cl− secretion. In our previous studies, [Cl−] i was shown to have a crucial role in cell proliferation and differentiation in gastric cancer cells [22, 23, 25], prostate cancer cells , osteoblast-like cells , breast cancer cell  and neural cells [18, 19]. These studies suggest that growth factors might control cell proliferation through regulation of NKCC expression and activity.
In this study, pretreatment with insulin alone did not stimulate transepithelial Cl− secretion in A6 cells, even though insulin upregulated mRNA expression of NKCC and CFTR. On the other hand, in the presence of forskolin, the enhancement of Cl− secretion by insulin was revealed. To stimulate transepithelial Cl− secretion, at least either the step of NKCC-mediated Cl− uptake or CFTR-mediated Cl− release in the Cl− secretion must be stimulated. This means that elevation of cAMP regulating NKCC and CFTR would be essentially required for stimulation of Cl− uptake or release contributing to the Cl− secretion.
In the present study, we observed that application of insulin alone upregulated mRNA expression of NKCC and CFTR; nevertheless, its application showed no stimulatory action on the basal Cl− secretion or apical Cl− channel conductance (activity). To clarify these phenomena, we speculated that proteins of NKCC and/or CFTR newly synthesized via insulin-elevated mRNA expression of NKCC and CFTR would stay in intracellular stores sites, but neither protein would be translocated to the apical or basolateral membrane only by insulin signaling. To confirm this speculation, we applied BFA (an inhibitor of protein translocation from ER to Golgi). As expected, BFA blocked the forskolin action on Cl− secretion and apical Cl− channel conductance (activity) (Fig. 8). Further, we should state that even in the absence of insulin application, BFA reduced the stimulatory action of forskolin [Fig. 8a, b; (+) BFA]. This means that irrespective of insulin application forskolin would have a stimulatory action on the translocation of NKCC and CFTR proteins to the apical and basolateral membrane. We strongly suggest that insulin shows its enhancing action on forskolin-stimulated Cl− secretion and apical Cl− channel conductance (activity) by upregulating mRNA expression of NKCC and CFTR but that the insulin signaling is not large enough for translocation of the insulin-induced newly synthesized proteins of NKCC and CFTR.
In A6 cells, insulin increased cell proliferation, which was abolished by bumetanide (an NKCC inhibitor) (Niisato et al. unpublished data). cAMP stimulates translocation of CFTR Cl− channels to the apical membrane and increases the number of functional CFTR Cl− channels detected by patch clamp techniques . Thus, insulin and cAMP cooperatively ativate Cl− transport regulating various cellular functions including epithelial Cl− secretion.
Taken together, these observations based on the present study suggest that: (1) insulin stimulates mRNA expression of NKCC and CFTR, which respectively contribute to transepithelial Cl− secretion as a Cl− uptake pathway across the basolateral membrane and a Cl− release pathway across the apical membrane; (2) the insulin-induced mRNA expression of NKCC and CFTR is respectively mediated through activation of PI3K stimulating NKCC mRNA expression and inactivation of ERK suppressing CFTR mRNA expression; (3) the insulin-increased NKCC and CFTR would be in the cytosolic store sites and cytosolic cAMP stimulates translocation of the insulin-increased NKCC and CFTR to the basolateral and apical membranes leading to an increases in transepithelial Cl− secretion associated with elevation of apical Cl− channel conductance (activity). Thus, insulin enhances the stimulatory action of cAMP on epithelial Cl− secretion via increases in new synthesis of NKCC and CFTR via PI3K- and ERK-mediated mechanisms (Fig. 9).
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This work was supported by Grants-in-Aid from the Japan Society of the Promotion of Science (24590283 to NN, 25670111 to YM), Salt Science (1235 to YM and NN) and Cell Research Conference to YM.
H. Sun and N. Niisato contributed equally to the present study.
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Sun, H., Niisato, N., Inui, T. et al. Insulin is involved in transcriptional regulation of NKCC and the CFTR Cl− channel through PI3K activation and ERK inactivation in renal epithelial cells. J Physiol Sci 64, 433–443 (2014). https://doi.org/10.1007/s12576-014-0338-3
- Cl− secretion