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J. Biol. Chem., Vol. 281, Issue 29, 20085-20094, July 21, 2006

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Cardiotonic Steroids Stimulate Glycogen Synthesis in Human Skeletal Muscle Cells via a Src- and ERK1/2-dependent Mechanism^*

Olga Kotova, Lubna Al-Khalili, Sara Talia, Catherine Hooke, Olga V. Fedorova, Alexei Y. Bagrov, and Alexander V. Chibalin¹

From the Section of Integrative Physiology, Department of Molecular Medicine and Surgery, Karolinska Institutet, SE-171 77 Stockholm, Sweden and the Laboratory of Cardiovascular Science, NIA, National Institutes of Health, Baltimore, Maryland 21224

Received for publication, February 17, 2005 , and in revised form, April 18, 2006.

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
The cardiotonic steroid, ouabain, a specific inhibitor of Na⁺,K⁺-ATPase, initiates protein-protein interactions that lead to an increase in growth and proliferation in different cell types. We explored the effects of ouabain on glucose metabolism in human skeletal muscle cells (HSMC) and clarified the mechanisms of ouabain signal transduction. In HSMC, ouabain increased glycogen synthesis in a concentration-dependent manner reaching the maximum at 100 nM. The effect of ouabain was additive to the effect of insulin and was independent of phosphatidylinositol 3-kinase inhibitor LY294002 but was abolished in the presence of a MEK1/2 inhibitor (PD98059) or a Src inhibitor (PP2). Ouabain increased Src-dependent tyrosine phosphorylation of ₁- and ₂-subunits of Na⁺,K⁺-ATPase and promoted interaction of ₁- and ₂-subunits with Src, as assessed by co-immunoprecipitation with Src. Phosphorylation of ERK1/2 and GSK3/, as well as p90rsk activity, was increased in response to ouabain in HSMC, and these responses were prevented in the presence of PD98059 and PP2. Incubation of HSMC with 100 nM ouabain increased phosphorylation of the-subunits of the Na-pump at a MAPK-specific Thr-Pro motif. Ouabain treatment decreased the surface abundance of ₂-subunit, whereas abundance of the ₁-subunit was unchanged. Marinobufagenin, an endogenous vertebrate bufadienolide cardiotonic steroid, increased glycogen synthesis in HSMC at 10 nM concentration, similarly to 100 nM ouabain. In conclusion, ouabain and marinobufagenin stimulate glycogen synthesis in skeletal muscle. This effect is mediated by activation of a Src-, ERK1/2-, p90rsk-, and GSK3-dependent signaling pathway.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
For almost 200 years cardiotonic steroids (CTS)² extracted from Digitalis purpurea were successfully used to treat patients with heart failure. Ouabain is one of the cardiac glycosides (obtained from the seeds of Strophanthus gratus), which specifically binds to and inhibits the activity of Na⁺,K⁺-ATPase, a plasma membrane cation pump, which is essential for maintenance of intracellular and extracellular sodium and potassium concentrations, cell volume, osmotic balance, and electrochemical gradients (1, 2). In addition to the cardiac glycosides of plant origin, the endogenous CTS were recently described as a new class of steroid hormones, endogenously produced in mammalian adrenal glands and central nervous system (3). Endogenous ouabain (EO) has been isolated as a stereoisomer of ouabain and identified as a constituent of human blood, bovine adrenal glands, and hypothalamus (3, 4) and circulates in elevated concentrations in the blood of 50% of Caucasians with high blood pressure (5). Bovine adrenal cortical cells in tissue culture release EO in response to norepinephrine, corticotropin, and angiotensin II (6, 7). Later, another mammalian endogenous CTS, a bufadienolide marinobufagenin (MBG), was found in human urine and plasma (8, 9). The plasma levels of MBG become elevated in several volume-expanded hypertensive states (10, 11). This hormone exhibits in vivo vasoconstrictor and natriuretic effects (10, 11). Importantly, exercise and stress cause an acute rise in the circulating levels of EO (12). Recent evidence from genetically engineered mice with modified cardiac glycoside binding affinity of the ₁- and ₂-subunits isoforms of the Na⁺,K⁺-ATPase indicate that the cardiac glycoside-binding site, which mediates the pharmacological effects of digitalis, is also the receptor for endogenous CTS (13).

Digitalis drugs appear to promote cardiac hypertrophy (14, 15). Similarly to other hypertrophic stimuli, ouabain regulates transcription of several hypertrophic marker genes in cardiac myocytes (16, 17). Recent evidence shows that in addition to a role in ion transport function, Na⁺,K⁺-ATPase can sense low concentrations of ouabain and play an important role as a signal transducer (18). Binding of Src to Na⁺,K⁺-ATPase forms a functional signaling complex (19). In cardiac myocytes, interaction of ouabain with the Na-pump causes activation of a Src, Ras/Raf, p42/44 MAPK signaling pathway, increases [Ca²⁺]_i, generates reactive oxygen species in mitochondria, and activates protein kinase C (PKC) isoforms (18). In renal cells Na⁺,K⁺-ATPase forms a cell signaling microdomain with inositol 1,4,5-trisphosphate receptor, which in the presence of ouabain, generates slow Ca²⁺ oscillations (20). Moreover, ouabain stimulates insulin-induced glycogen synthesis and decreases the production of CO₂ in rat diaphragm (21). However, mechanisms of ouabain signaling in skeletal muscle are unknown.

Because skeletal muscle contains one of the largest pools of Na⁺,K⁺-ATPase in the body (22), the signal transduction effects mediated by ouabain in skeletal muscle may have a profound metabolic impact. However, the rodent ₁-subunit isoform is resistant to ouabain (23). Therefore, the concentrations of ouabain used in experiments with rat muscles (21) were much higher than concentrations of endogenous CTS observed under physiological conditions. Human ₁- and ₂-subunits exhibit relatively high affinity to ouabain (24). Nanomolar concentrations of MBG bind to the human Na⁺,K⁺-ATPase, and in human vascular sarcolemma, which expresses ₁-subunit of Na⁺,K⁺-ATPase, MBG exhibits greater Na⁺,K⁺-ATPase inhibitory activity as compared with that of ouabain (25). Thus, a study of the effect of ouabain and MBG on glucose metabolism in skeletal muscle cells of human origin was of interest. Therefore, the aim of this study was to investigate the effects of ouabain and MBG on glycogen synthesis in human skeletal muscles cells (HSMC) and to identify the mechanisms of CTS signal transduction.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Antibodies and Reagents—Ouabain was obtained from Sigma. Marinobufagenin was purified from Bufo marinus toad venom, as described previously (26). Insulin (Actrapid) was from Novo Nordisk (Denmark). MEK1/2 inhibitor PD98059 (2'-amino-3'-methoxyflavone), c-Src inhibitor PP2 (4-amino-5-[4-chlorophenyl]-7-[t-butyl] pyrazolo[3,4-d]-pyrimidine), and PI 3-kinase inhibitor LY294002 (2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one) were from Calbiochem. Rabbit polyclonal antibodies to phospho-GSK3/ (Ser²¹ of GSK3 and Ser⁹ of GSK3), phospho-c-Src (Tyr⁴¹⁶), phospho-p90rsk (Thr⁵⁷³), phospho-PKC/ (Thr^638/641), phospho-SAPK/JNK (Thr¹⁸³/Tyr¹⁸⁵), phospho-p38 MAPK (Thr¹⁸⁰/Tyr¹⁸²), phospho-AMPK (Thr¹⁷²), phospho-CaMKII (Thr²⁸⁶), and monoclonal antibody to phospho-Thr-Pro motif were from Cell Signaling Technology, Inc. (Beverly, MA). Rabbit polyclonal antibodies to phospho-ERK1/2 (Tyr²⁰⁴) and phospho-Akt/PKB (Ser⁴⁷³) were from New England Biolabs Inc. (Beverly, MA). Rabbit polyclonal antibody to c-Src was from Santa Cruz Biotechnology, Inc. Rabbit polyclonal antibody to phospho-Tyr was from BD Transduction Laboratories. Mouse monoclonal and rabbit polyclonal antibodies to ₁-subunit of Na⁺,K⁺-ATPase were a kind gift from Dr. M. Caplan (Yale University, New Haven, CT). Mouse monoclonal antibody to ₂-subunit of Na⁺,K⁺-ATPase was a kind gift from Dr. K. Sweadner (Massachusetts General Hospital, Charlestown, MA), rabbit polyclonal antibody to ₂-subunit of Na⁺,K⁺-ATPase was the kind gift from Dr. T. Pressley (Texas Tech University Health Sciences Center, Lubbock, TX). Rabbit polyclonal antibody to p90rsk was a kind gift from Dr. D. Alessi (University of Dundee, Dundee, Scotland). Horseradish peroxidase-conjugated goat anti-rabbit and anti-mouse immunoglobulin G was obtained from Bio-Rad. Protein A-Sepharose CL-4B and horseradish peroxidase-linked protein A were from Amersham Biosciences. Protein-L-agarose and protein G-Sepharose were from Sigma. Reagents for enhanced chemiluminescence were obtained from Amersham Biosciences. Streptavidin-agarose beads and EZ-link Sulfo-NHS-SS-biotin were from Pierce. Cross-tide (Gly-Arg-Pro-Arg-Thr-Ser-Ser-Phe-Ala-Glu-Gly) was from Sigma-Aldrich. Cell culture media and reagents were from Invitrogen. Dimethyl sulfoxide (Calbiochem) was used as a solvent for protein kinases inhibitors. All other reagents were of analytical grade (Sigma).

Cell Culture—Human skeletal muscle satellite cells were isolated from muscle biopsies and cultured, as previously described (27). The experiments were performed on passages 3 and 4. To initiate differentiation into myotubes, Ham's F-10 medium with 20% FBS was removed from cells, and DMEM containing 1% PeSt (100 units/ml penicillin, 100 mg/ml streptomycin (Invitrogen)) and 4% FBS were added for 48 h. The medium was changed to DMEM containing 1% PeSt and 2% FBS. Fusion and multinucleation of the cells was observed at day 3 after initiation of the differentiation protocol. Glucose uptake in HSMC was measured, as previously described (28).

Glucose Incorporation into Glycogen—Myoblasts were seeded 1500 cells/well in 6-well plates and differentiated at 70–80% confluence. Differentiated myotubes (5–7 days) were serum-starved (DMEM + 0% FBS) overnight prior to the experiment to reduce the basal level of insulin- and cytokine-dependent kinase activity. Cells were preincubated with 1) 22 µM PD98059, 20 µM PP2, 10 µM LY294002, or Me₂SO for 20 min, then incubated with 100 nM ouabain for 10 min, and finally stimulated with 120 nM insulin for 20 min at 37 °C in 950 µl of serum-free DMEM; 2) cells were incubated with ouabain or marinobufagenin for 30 min; or 3) cells were preincubated with 22 µM PD98059, 20 µM PP2, 10 µM LY294002, or Me₂SO for 20 min, and then ouabain, marinobufagenin, insulin or Me₂SO were added. Thereafter, 50 µl of the isotope solution (D-[U-¹⁴C] glucose with 1 µCi/ml; final specific activity, 0.18 µCi/µmol in DMEM) was added, and the plates were incubated for 30 min. The reactions were terminated by placing the plates on ice. The medium was aspirated, and the wells were washed with ice-cold PBS three or four times. The plates were frozen directly after at –80 °C, or myotubes were solubilized with 1 ml 0.03% SDS for 1 h at room temperature. Aliquots (0.85 ml) of the suspension was transferred to 10-ml tubes, and 100 µl (2 mg) of carrier glycogen was added. The remained suspension was used for protein concentration determination. The samples were boiled for 30 min. A 3-ml solution of 98% ethanol was added to precipitate glycogen. Tubes were incubated overnight at 4 °C with slight agitation and centrifuged at 5000 x g for 35 min at 4 °C. Pellet was washed once with 70% ethanol, samples were centrifuged at 5000 x g for 10 min, and ethanol was aspirated off. The pellet was solubilized in 200 µl of distilled H₂O and transferred to 4-ml scintillation vials. Samples and aliquots of the media were counted in a liquid scintillation counter (1214 Rackbeta; Wallac, Turku, Finland).

Measurement of Ouabain-sensitive ⁸⁶Rb⁺ Uptake—The initial rate of ouabain- or marinobufagenin-sensitive ⁸⁶Rb⁺ uptake through Na⁺,K⁺-ATPase of HSMC was measured as previously described (29). Uptake that was inhibited by 100 µM ouabain was taken as the maximal rate of active uptake.

Western Blot Analysis—HSMC were lysed in 500 µl of homogenization buffer (137 mM NaCl, 2.7 mM KCl, 1 mM MgCl₂, 20 mM Tris, pH 8.0, 1% Triton X-100, 10% (v/v) glycerol, 10 mM NaF, 0.5 mM Na₃VO₄,5 µg/ml leupeptin, 0.2 mM phenylmethylsulfonyl fluoride, 5 µg/ml aprotinin, and 1 µM microcystin) on the rotation wheel at 4 °C during 1 h. Then samples were centrifuged at 12,000 x g for 10 min, 4 °C. The supernatants were collected, and the protein concentration was measured, using BCA^TM protein assay kit (Pierce). The samples were prepared for SDS-PAGE (7.5 or 10% resolving gel). The proteins were transferred to polyvinylidene difluoride membranes and blocked with 7.5% nonfat milk in Tris-buffered saline with Tween 20. The membranes were incubated with primary antibodies overnight at 4 °C on a shaking platform. The membranes were washed with Tris-buffered saline with Tween 20 and incubated with anti-rabbit or anti-mouse secondary antibody or protein A conjugate with horseradish peroxidase. The proteins were visualized by ECL and quantified by densitometry.

Immunoprecipitation—Cell lysates (500 µl) were incubated with 40 µl of protein A-Sepharose beads, with rotation for 30 min at 4 °C. After brief centrifugation, the supernatants were collected and immunoprecipitated with 1) antibodies to c-Src overnight at 4 °C and 2) antibodies to p-Tyr overnight at 4 °C. The immunoprecipitates were collected on protein A-Sepharose beads for 2 h at 4°C. HSM myotubes lysates (300 µg of protein) were immunoprecipitated for 2.5 h at 4 °C with anti-phospho-Thr-Pro mouse IgM. Immunoprecipitates were collected on protein-L-agarose beads. For immunoprecipitations, the beads were washed three times in homogenization buffer and twice in ice-cold PBS. The pellets were resuspended in Laemmli sample buffer.

Cell Surface Biotinylation—Myotubes (6 day) were preincubated in PBS in the absence or presence of 100 nM ouabain for 1 h and thereafter exposed to EZ-link Sulfo-NHS-SS-biotin at a final concentration of 1.5 mg/ml in PBS at 4 °C for 60 min with gentle shaking. Cell surface biotinylation was performed as described (27). After streptavidin precipitation, the samples were analyzed by SDS/PAGE with subsequent Western blot with appropriate antibodies.

p90rsk Activity Assay—Cultured myotubes treated with 100 nM ouabain for 2 h in the presence or absence of inhibitors PD98059 and PP2 were analyzed. Myotube lysates (100 µg of protein/sample) were immunoprecipitated at 4 °C overnight with anti-p90rsk antibody, previously equilibrated with protein G-Sepharose in homogenization buffer. Immunoprecipitates were washed three times in homogenization buffer, containing 0.5 M NaCl and twice in buffer B (50 mM Tris-HCl, pH 7.5, 0.03% Brij-35, 0.1 mM EGTA, 0.1% -mercaptoethanol). The samples were resuspended in 30 µl of kinase buffer (50 mM Tris-HCl, pH 7.5, 0.1 mM EGTA, 0.1% -mercaptoethanol, 17 µM cAMP-dependent protein kinase inhibitor peptide, 16.7 mM Mg(Ac)₂, 50 µM cross-tide, and 2 µCi of [-³²P]ATP) and incubated at 30 °C for 10 min. The reactions were terminated on ice by the addition of sample buffer (125 mM Tris, 6 M urea, pH 6.8). Reaction products were resolved on a 40% acrylamide gel, and ³²P_i incorporation into peptide substrate was analyzed by exposing gels to a phosphorimaging device (Fuji BAS-1800II).

View larger version (54K): [in this window] [in a new window]   FIGURE 1. Dose-dependent response of HSMC to ouabain. Human skeletal muscle cells were incubated with increasing concentrations of ouabain (10 nM, 100 nM, and 1 µM) for 30 min. A, [U-14C]glucose incorporation into glycogen was measured as described under "Experimental Procedures." The values are the means ± S.E. (n = 6). *, p < 0.05 versus basal. B, dose-dependent inhibition of total 86Rb+ uptake by ouabain. The assay was performed as described under "Experimental Procedures." The results are the means ± S.E. for six independent experiments performed in duplicate. *, p < 0.05 versus control. C, phosphorylation of the protein kinases c-Src, Akt/PKB, PKC/, c-JNK, p38 MAPK, ERK1/2, p90rsk, GSK3/, AMPK, and CaMKII in response to ouabain in HSMC. Representative blots from four independent experiments are shown.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Effect of Ouabain on Glycogen Synthesis and Cell Signaling—HSMC were incubated with different concentrations of ouabain (10 nM, 100 nM, and 1 µM) to assess the effect of ouabain on glycogen synthesis. [U-¹⁴C]Glucose incorporation into glycogen was stimulated in a dose-dependent manner, with a significant increase (p < 0.05) from basal in the presence of 100 nM of ouabain, with no further change in the presence of increasing concentrations of ouabain (Fig. 1A). Muscle cells were exposed to ouabain for a 30-min incubation time to allow for measurable [U-¹⁴C]glucose incorporation into glycogen. Ouabain (100 nM) caused a 16% statistically insignificant inhibition of total ouabain-sensitive ⁸⁶Rb⁺ uptake (Fig. 1B) in human myotubes (inhibition of ⁸⁶Rb⁺ uptake achieved at 100 µM of ouabain was considered as 100% of ouabain-sensitive ⁸⁶Rb⁺ uptake).

To identify the mechanisms of ouabain signal transduction toward glycogen synthesis in human skeletal muscle cells, we assess phosphorylation of an array of protein kinases previously implicated in ouabain-induced signal transduction (18) and regulation of glycogen synthesis (30). Phosphorylation of Src, ERK1/2, p90rsk, and GSK3/ increased in a dose-dependent manner in response to ouabain, reaching the maximum at 100 nM after a 30-min incubation, whereas phosphorylation of the stress-activated MAPKs, c-JNK and p38 was unchanged. Ouabain (100 nM) stimulates Src, ERK1/2, p90rsk, and GSK3 phosphorylation already after 15 min of incubation (data not shown). Notably, phosphorylation of Akt/PKB was unaffected by ouabain. PKC/ phosphorylation was slightly decreased in the presence of 100 nM or higher concentration of ouabain (Fig. 1C). Because ouabain inhibition of the Na⁺,K⁺-ATPase may lead to local changes in ATP concentrations and an increase in [Ca²⁺]_i, we assessed also phosphorylation of AMPK and CaMKII in response to ouabain. AMPK and CaMKII phosphorylation was unchanged in response to ouabain. Thus, in HSMC ouabain, in concentrations that are unable to significantly decrease Na-pump activity, stimulates glycogen synthesis, activates c-Src, ERK1/2-p90rsk, and leads to phosphorylation of GSK3/. Based on the results, ouabain at a concentration of 100 nM was used for stimulation of human muscle cells studying subsequent experiments.

View larger version (45K): [in this window] [in a new window]   FIGURE 2. Na+,K+-ATPase -subunits tyrosine phosphorylation and interaction with Src in response to ouabain. HSMC were incubated in the presence or absence of 100 nM ouabain and inhibitors PD98059 (22 µM) and PP2 (20 µM), under basal () or insulin-stimulated () (120 nM) conditions. The cell lysates were immunoprecipitated with anti-phosphotyrosine antibodies and blotted with antibodies against 1- and 2-subunit of Na+,K+-ATPase as described under "Experimental Procedures." Representative Western blots (upper panels) and quantitative data (means ± S.E.) (lower panels) for 1-subunit (A) and 2-subunit (B) are shown (n = 5). Na+,K+-ATPase -subunits co-immunoprecipitate with anti-Src antibodies. The cell lysates were precipitated with anti-Src antibodies and blotted with antibodies against 1- and 2-subunit of Na+,K+-ATPase as described under "Experimental Procedures." Representative Western blots (upper panels) and quantitative data (means ± S.E.) (lower panels) for 1-subunit (C) and 2-subunit (D) are shown (n = 5). *, p < 0.05 versus basal without ouabain; , p < 0.05 versus insulin-stimulated without ouabain; #, p < 0.05 versus ouabain without the inhibitor.

To assess interaction of Src with Na⁺,K⁺-ATPase, we immunoprecipitated Src from cell lysates and analyzed co-precipitated Na⁺,K⁺-ATPase -subunits by Western blot. The amount of immunoprecipitated Src was unaffected by conditions during cell stimulation (data not shown). ₁- and ₂-subunits were co-immunoprecipitated with c-Src at the basal, unstimulated condition. Insulin increased the amount of -subunits co-immunoprecipitated with Src (Fig. 2, C and D). Co-immunoprecipitation of the ₁- and ₂-subunits of the Na-pump with Src was markedly increased after stimulation with ouabain, in the absence or presence of insulin. This effect of ouabain was diminished by PP2 and was unaffected by PD98059. Taken together, these findings suggest that ouabain stimulates Na⁺,K⁺-ATPase -subunit phosphorylation on tyrosine residues and facilitates complex formation of Na⁺,K⁺-ATPase with Src. The Na⁺,K⁺-ATPase-Src interaction partially depends on tyrosine phosphorylation of the pump -subunits.

View larger version (19K): [in this window] [in a new window]   FIGURE 3. Ouabain-stimulated glycogen synthesis in human skeletal muscle cells is PI 3-kinase independent. A, glycogen synthesis (HSMC) in the presence or absence of 100 nM ouabain and PI 3-kinase inhibitor LY294002 (10 µM), under basal () or insulin-stimulated () (120 nM) conditions. [U-14C]Glucose incorporation into glycogen was measured as described under "Experimental Procedures." The values are the means ± S.E. (n = 6). *, p < 0.05 versus basal without ouabain versus control without LY294002; , p < 0.05 versus insulin-stimulated without ouabain; #, p < 0.05 versus ouabain without the inhibitor. B, Akt/PKB phosphorylation in response to 100 nM ouabain in basal () and insulin-stimulated () conditions (120 nM). A representative blot (upper panel) and the quantitative data (means ± S.E.) (lower panels) are shown.

GSK3 can also be phosphorylated by a downstream kinase of classical MAPK cascade, p90rsk (MAPKAP-K1) (30), which is phosphorylated by ERK1/2. In HSMC, insulin increases ERK1/2 phosphorylation and p90rsk activity. The effect of insulin was abolished by the MEK1/2 inhibitor PD98059 and was unaffected by the Src inhibitor PP2 (Fig. 4, A and B). Additional stimulation with ouabain leads to an increase in basal and insulin-stimulated ERK1/2 phosphorylation and p90rsk activity (Fig. 4, A and B). The effect of ouabain on MAPK activation was additive to the effect of insulin. Preincubation of insulin- and/or ouabain stimulated myotubes with PD98059 abolished all stimulatory effects, whereas incubation with PP2 restored ERK1/2 phosphorylation and p90rsk activity to levels achieved without ouabain. These results indicate that in HSMC, p90rsk can be activated by insulin or, independently and additively to insulin, by ouabain via c-Src stimulation.

As expected, insulin stimulates GSK3 phosphorylation and increases [U-¹⁴C]glucose incorporation into glycogen. PD98059 and PP2 had no effect on GSK3 phosphorylation and glycogen synthesis under basal and insulin-stimulated conditions (Fig. 4, C and D). Ouabain (100 nM) profoundly stimulated GSK3 phosphorylation and increased [U-¹⁴C]glucose incorporation into glycogen under basal and insulin-stimulated conditions, and this effect was additive to the effect of insulin. The effect of ouabain on GSK3 phosphorylation and glycogen synthesis was abolished by PD98059 and PP2 (Fig. 4D).

Our findings provide evidence to suggest that in human differentiated myotubes, glycogen synthesis can be activated by insulin via PI 3-kinase-Akt pathway or independently to insulin action by ouabain via PI 3-kinase-independent, Src-activated MAPK signaling cascade.

Effect of Marinobufagenin on HSMC—To evaluate the physiological significance of ouabain-induced stimulation of glycogen synthesis in HSMC, it was of interest to compare the effect of ouabain with an effect of an endogenous CTS. Human myotubes were incubated with an endogenous bufadienolide, MBG. MBG (1 nM) insignificantly (17% above control) increased glycogen synthesis, whereas 10 nM MBG stimulated [U-¹⁴C]glucose incorporation into glycogen similarly to 100 nM ouabain (Fig. 5A). Increased concentrations of MBG did not further increase glycogen synthesis (data not shown). MBG at 1 and 10 nM inhibited total ouabain-sensitive ⁸⁶Rb⁺ uptake 15 and 21%, respectively (Fig. 5B). This inhibition was similar to that of 100 nM ouabain (Fig. 1B). Western blot analysis of lysates prepared from HSMC incubated for 30 min with 10 nM MBG and 100 nM ouabain revealed a similar increase in the phosphorylation of c-Src, ERK1/2, p90rsk, and GSK3/ (Fig. 5C). Akt/PKB phosphorylation was unaffected by MBG. In contrast to ouabain, PKC/ phosphorylation was unaltered in the presence of 10 nM MBG. Thus, in human myotubes, the endogenous bufadienolide CTS, MBG, exhibits an effect similar to that of ouabain, but at lower range of concentrations.

Cell Surface Abundance of Na-pump Subunits in Response to Ouabain—In our previous study (29), insulin increased the phosphorylation of the -subunits of Na-pump in an ERK1/2-dependent manner. Because ouabain signal transduction involves activation of the MAPK pathway, we determined whether the human Na-pump is phosphorylated by ERK1/2. HSMC lysates were immunoprecipitated with an antibody against phospho-Thr-Pro motif, which is an ERK phosphorylation site, and thereafter the samples were blotted with antibodies against ₁- and ₂-subunits of Na⁺,K⁺-ATPase. Phosphorylation of the -subunits was significantly increased in response to 100 nM ouabain (Fig. 6A).

ERK1/2 phosphorylation of Na⁺,K⁺-ATPase -subunits regulates Na-pump cell surface abundance (29, 32). We utilized a biotinylation technique to assess the cell surface abundance of Na-pump -subunits in response to ouabain. We have shown that after 1 h of incubation of cells with ouabain, the cell surface content of the ₂-subunit is significantly decreased, whereas the cell surface abundance of the ₁-subunit was unaffected (Fig. 6B). Inhibition of MEK1/2 by PD98059 decreased the Na-pump -subunit cell surface abundance under basal conditions and enhanced the ouabain-stimulated disappearance of the ₂-subunit from the plasma membrane (Fig. 6B), suggesting that ERK1/2-mediated signaling is important for Na-pump endocytosis.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 
Ouabain is a cardiac glycoside and a specific inhibitor of Na⁺,K⁺-ATPase. A role for digitalis glycosides to improve cardiac contractility is well established, because inhibition of Na-pump leads to an increase in [Na⁺]_i and an elevation of [Ca²⁺]_i because of the activation of the Na⁺-Ca²⁺ exchanger (33, 34). Recent reports (16, 20, 35–38) provide evidence for a novel mechanism of ouabain-dependent signaling in cardiac myocytes and kidney cells. Whether ouabain acts as a signal transducer in skeletal muscle still remains unclear.

In human differentiated myotubes ouabain increased [U-¹⁴C]glucose incorporation into glycogen in a dose-dependent manner. This effect was additive to insulin and diminished in the presence of a MEK1/2 inhibitor (PD98059) or a Src inhibitor (PP2). Ouabain activates glycogen synthesis in concentrations that only slightly decrease a Na-pump activity in HSMC. Ouabain was without effect on AMPK and CaMKII phosphorylation, indicating that intracellular ATP/AMP ratio and [Ca²⁺]_i were unaffected by ouabain. Interestingly, PKC/ phosphorylation was decreased in the presence of 100 nM or higher concentrations of ouabain, a finding that contrasts previous data obtained on rat cardiomyocytes, where ouabain activates Ca²⁺-dependent PKCs (39). Ouabain (100 nM) does not affect [Na⁺]_i in the human breast cancer cells (35). Importantly, incubation of HSMC in potassium-free medium, which would inhibit the Na-pump activity, does not promote glycogen synthesis (data not shown). There is no experimental evidence for a membrane receptor for cardiac glycosides that differs from Na⁺,K⁺-ATPase. Thus, the ouabain-induced effects in HSMC appear not to be secondary to the Na-pump inhibition, but rather a consequence of ouabain binding to a fraction of Na-pumps in skeletal muscle. Indeed, even under conditions of low occupancy, receptors effectively transmit signals inside a cell. Alternatively, low concentration of ouabain may target a "high affinity" binding site that is present only in a signaling complex formed by Na⁺,K⁺-ATPase and functionally different from the well characterized "low affinity" inhibitory binding site (40).

View larger version (39K): [in this window] [in a new window]   FIGURE 4. ERK1/2 phosphorylation (A), p90rsk activity (B), GSK3 / phosphorylation (C), and glycogen synthesis (D) in HSMC under basal ([squlo]) or insulin-stimulated () (120 nM) conditions in the presence or absence of 100 nM ouabain and inhibitors PD98059 and PP2. HSMC were incubated in the absence or presence of 100 nM ouabain and 22 µM PD98059 and 20 µM PP2 under basal or insulin-stimulated (120 nM) conditions. Western blot analysis of cell lysates, p90rsk activity assay, and [U-14C]glucose incorporation into glycogen were performed as described under "Experimental Procedures." Representative blots and autoradiogram (upper panels) and quantitative data (means ± S.E.) (lower panels) are shown (n = 6). *, p < 0.05 versus basal without ouabain; , p < 0.05 versus insulin-stimulated without ouabain.

View larger version (47K): [in this window] [in a new window]   FIGURE 5. The effect of marinobufagenin on HSMC. Human skeletal muscle cells were incubated with 100 nM ouabain or 10 nM MBG. A, [U-14C]glucose incorporation into glycogen was measured as described under "Experimental Procedures." The values are the means ± S.E. (n = 5). *, p < 0.05 versus control. B, dose-dependent inhibition of total 86Rb+ uptake by MBG. The assay was performed as described under "Experimental Procedures." The results are the means ± S.E. for nine independent experiments performed in duplicate. *, p < 0.05 versus control. C, phosphorylation of the array of proteins: c-Src, Akt/PKB, PKC/, ERK1/2, p90rsk, GSK3/ in response to MBG or ouabain in HSMC. Representative blots from four independent experiments are shown.

The Src inhibitor PP2 blocks insulin- and ouabain-stimulated tyrosine phosphorylation of the pump -subunits. Tyrosine phosphorylation of Na⁺,K⁺-ATPase ₁- and ₂-subunits in response to insulin by an unidentified kinase has been previously reported (47, 48). Src phosphorylates the Na⁺,K⁺-ATPase ₁-subunit in vitro (40, 49). Thus, the tyrosine kinase that phosphorylates the Na⁺,K⁺-ATPase -subunits in response to insulin can be Src. Interestingly, insulin-stimulated tyrosine phosphorylation of the Na⁺,K⁺-ATPase -subunit leads to an increase in the enzyme affinity to Na⁺ and increases pump activity. Therefore, tyrosine phosphorylation of -subunit could explain the paradoxical increase in the pump activity in response to subnanomolar concentration of ouabain or endogenous CTS (40).

Activation of Src increases MAPK signaling (18). Src catalyzes the phosphorylation and activation of c-Raf, which leads to an activation of p42/p44 MAPK (50). In cardiac myocytes, ouabain increases MAPK signaling and thereby affects gene transcription and translation (18). Ouabain also acts as the potent promoter of growth via ERK1/2 activation in rat kidney epithelial cells (36). Ouabain stimulates ERK1/2 phosphorylation under basal and insulin-stimulated conditions in human skeletal muscle cells. ERK1/2 activation leads to activation of p90rsk, a downstream effector of MAPK (51). Similarly in HSMC, ouabain stimulates p90rsk activity and phosphorylation.

Serine residue near the amino terminus of GSK3 (Ser²¹ of GSK3 and Ser⁹ of GSK3) are the main target of PKB/Akt. Active GSK3 (dephosphorylated) inhibits glycogen synthase. Phosphorylation and inhibition of GSK3 promotes dephosphorylation and activation of glycogen synthase and promotes glycogen synthesis. In addition to Akt/PKB, p70 ribosomal S6 kinase, and p90rsk phosphorylates GSK3/ on Ser^21/9 and inhibits GSK3 (52, 53). In Swiss 3T3 cells, phorbol myristate acetate and epidermal growth factor leads to phosphorylation and inhibition of GSK3 via activation of MAPK signaling pathway and p90rsk (54). Because ouabain-stimulated glycogen synthesis was unaffected by inhibition of PI 3-kinase-Akt/PKB signaling pathway, with a profound increase in p90rsk activity, we hypothesize that in HSMC, ouabain can stimulate GSK3 phosphorylation and glycogen synthesis via p90rsk.

View larger version (37K): [in this window] [in a new window]   FIGURE 6. Effect of ouabain on Thr-Pro sequence motif phosphorylation and cell surface abundance of -subunits of Na-pump in HSMC. A, phosphorylation of -subunits of Na-pump on Thr-Pro motif in response to 100 nM ouabain in HSMC. Cell lysates were immunoprecipitated (IP) with antibodies to phospho-Thr-Pro motif and subjected to Western blot (WB) with 1- and 2-subunits of Na+,K+-ATPase. Representative blots (upper panels) and quantitative data (means ± S.E.) (lower panels) are shown (n = 5). B, cell surface abundance of Na+,K+-ATPase -subunits in HSMC in response to 1 h of exposure to 100 nM ouabain in the absence or presence of 22 µM PD98059. Cell surface biotinylation, precipitation of cell lysates with streptavidin-agarose beads, and Western blot analysis were performed as described under "Experimental Procedures." Representative blots (upper panels) and quantitative data (means ± S.E.) (lower panels) are shown (n = 5). *, p < 0.05 versus control.

Exercise and stress cause an acute rise in EO circulating levels (55). EO release from the adrenal cortical cells is stimulated by angiotensin II and catecholamines. In humans, EO peaked immediately after a 15-min cycling exercise and return to basal level 1 h thereafter (6). In rats subjected to acute stress by swimming, the circulating levels of EO peaked within 40 min after stress and returned to basal level at 70 min. Therefore, the stimulatory effect of EO on glycogen synthesis in skeletal muscle may have physiological relevance and may constitute a mechanism for the adaptive response to exercise. Heightened EO levels may activate glycogen synthesis immediately after exercise, when insulin levels are low.

View larger version (14K): [in this window] [in a new window]   FIGURE 7. Schematic representation of intracellular signaling pathways for cardiotonic steroids in human skeletal muscle cells.

Activation of ERK1/2 MAPK is an important step in regulation of Na⁺,K⁺-ATPase (29, 32). In porcine proximal tubular cells (LLC-PK1), ouabain stimulates clathrin-dependent endocytosis of the ₁-subunit to intracellular compartments (59). Incubation of HSMC with 100 nM ouabain increased phosphorylation of -subunits of Na-pump on a MAPK-specific Thr-Pro motif. After ouabain exposure the ₁-subunit cell surface abundance was unaltered, whereas the ₂-content was decreased (Fig. 6B). This observation is consistent with the hypothesis that in skeletal muscle, the ₂-subunit is subjected to tighter regulation in response to different stimuli compare with ₁. Taking into account a relatively high expression of ₂ in HSMC, this observation may point out a possible mechanism of desensitization of ouabain signaling.

Phosphorylation of Na⁺,K⁺-ATPase -subunits by ERK1/2 MAPK can provide a positive feedback mechanism on pump activity in skeletal muscle (Fig. 7). This may be especially important when the Na-pump is partially inhibited by cardiotonic steroids. We hypothesize that phosphorylation of Na⁺,K⁺-ATPase -subunit by ERK1/2 arrests the formation of an endocytic complex consisting of Na⁺,K⁺-ATPase, adaptor proteins, and clathrin, thereby preventing Na⁺,K⁺-ATPase endocytosis and increasing the plasma membrane -subunit abundance caused by constitutive exocytosis. Indeed, inhibition of the ERK1/2 signaling pathway promotes -subunit disappearance from the cell surface under basal conditions and augments an ouabain-stimulated decrease in ₂-subunit cell surface abundance (Fig. 6B). Interaction of Na⁺,K⁺-ATPase -subunit and clathrin adaptor protein 2 is disturbed, whereas -subunit is phosphorylated by ERK1/2.³

In conclusion, our studies provide evidence that the cardiotonic steroids ouabain and MBG increase glycogen synthesis, additively to insulin in skeletal muscle. This effect is mediated by activation of a Src-, ERK1/2-, p90rsk-, and GSK3-dependent signaling pathway and may constitute a physiological relevant feedback mechanism of adaptation of skeletal muscle to exercise. We also propose that digitalis drugs may have a beneficial side effect to enhance insulin action in skeletal muscle. Elucidation of the signal transducer function of the Na⁺,K⁺-ATPase in skeletal muscle may have important clinical implications for delineating the mechanisms involved in the development of muscle fatigue, cardiovascular diseases, and complications of diabetes mellitus.

	FOOTNOTES

 
^* This work was supported by grants from the Swedish Research Council, the Swedish Heart and Lung Foundation, the Novo-Nordisk Foundation, the Swedish Society of Medicine, and the NIA, National Institutes of Health Intramural Research Program. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

¹ To whom correspondence should be addressed: Dept. of Molecular Medicine and Surgery, Section of Integrative Physiology, Karolinska Institutet, von Eulers väg 4, 4 tr, SE-171 77, Stockholm, Sweden. Tel.: 46-8-524-87-584; Fax: 46-8-335436; E-mail: Alexander.Chibalin{at}ki.se.

² The abbreviations used are: CTS, cardiotonic steroid(s); EO, endogenous ouabain; HSMC, human skeletal muscle cell(s); GSK, glycogen synthase kinase; ERK, extracellular signal-regulated kinase; MAPK, mitogen-activated protein kinase; MBG, marinobufagenin; PI, phosphatidylinositol; PKC, protein kinase C; FBS, fetal bovine serum; DMEM, Dulbecco's modified Eagle's medium; PBS, phosphate-buffered saline; CaMK, calmodulin kinase; AMPK, AMP-activated protein kinase.

³ O. Kotova and A. V. Chibalin, unpublished results.

	ACKNOWLEDGMENTS

 
We thank Dr. Michael Caplan, Dr. Kathleen Sweadner and Dr. T. Pressley for the kind gift of anti-₁- and anti-₂-subunits antibodies. We are grateful to Dr. Juleen R. Zierath, Dr. Anna Krook, Dr. Marc Gilbert, and Dr. Amir Askari for helpful discussions and critical reading of the manuscript. We thank Dr. Karim Bouzakri and Anna Zachrisson for culturing HSMC.

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TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

 

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