Research Article | Open Access
Effect of Exercise Intensity on Isoform-Specific Expressions of NT-PGC-1α mRNA in Mouse Skeletal Muscle
PGC-1α is an inducible transcriptional coactivator that regulates mitochondrial biogenesis and cellular energy metabolism in skeletal muscle. Recent studies have identified two additional PGC-1α transcripts that are derived from an alternative exon 1 (exon 1b) and induced by exercise. Given that the PGC-1α gene also produces NT-PGC-1α transcript by alternative 3′ splicing between exon 6 and exon 7, we have investigated isoform-specific expression of NT-PGC-1α mRNA in mouse skeletal muscle during physical exercise with different intensities. We report here that NT-PGC-1α-a mRNA expression derived from a canonical exon 1 (exon 1a) is increased by high-intensity exercise and AMPK activator AICAR in mouse skeletal muscle but not altered by low- and medium-intensity exercise and β2-adrenergic receptor agonist clenbuterol. In contrast, the alternative exon 1b-driven NT-PGC-1α-b (PGC-1α4) and NT-PGC-1α-c are highly induced by low-, medium-, and high-intensity exercise, AICAR, and clenbuterol. Ectopic expression of NT-PGC-1α-a in C2C12 myotube cells upregulates myosin heavy chain (MHC I, MHC II a) and Glut4, which represent oxidative fibers, and promotes the expression of mitochondrial genes (Cyc1, COX5B, and ATP5B). In line with gene expression data, citrate synthase activity was significantly increased by NT-PGC-1α-a in C2C12 myotube cells. Our results indicate the regulatory role for NT-PGC-1α-a in mitochondrial biogenesis and adaptation of skeletal muscle to endurance exercise.
PGC-1α is an inducible transcriptional coactivator that regulates cellular energy metabolism and metabolic adaptation to environmental and nutritional stimuli [1–3]. PGC-1α is induced in muscle by exercise and regulates energy metabolism and structural adaptation of muscle to exercise [4, 5]. PGC-1α stimulates many of the best-known beneficial effects of exercise in muscle: mitochondrial biogenesis, angiogenesis, and fiber-type switching [5, 6]. The health benefits of elevated expression of PGC-1α in muscle may go beyond the muscle tissue itself. The contracting muscle secretes myokines that participate in tissue crosstalk. PGC-1α promotes the production of newly identified hormone irisin from exercised muscle, increasing energy expenditure with no changes in movement or food intake . Another contraction-induced myokine, beta-aminoisobutyric acid (BAIBA), induces browning of white adipose tissue and increases fat oxidation in the liver . They could be therapeutics for human metabolic disease and other disorders that are improved with exercise.
Transcription of the PGC-1α gene can be driven by two different promoters in mouse and human skeletal muscle and adipose tissue [9, 10]. A proximal promoter is located upstream of a canonical exon 1 (exon 1a) and a distal promoter followed by an alternative exon 1 (exon 1b) is located ~13.7 kb upstream from the exon 1a of the PGC-1α gene (Figure 1(a)) . The PGC-1α-b and PGC-1α-c transcripts are derived by alternative splicing of the exon 1b at two different 5′ splice sites to the canonical exon 2, producing two PGC-1α isoforms, PGC-1α-b and PGC-1α-c, which actually have different N termini with the first 16 aa of PGC-1α-a being replaced by 12 aa and 3 aa alternate protein sequence in PGC-1α-b and PGC-1α-c, respectively (Figure 1(c)). PGC-1α-b and PGC-1α-c are functionally active and induce PPAR-dependent transcription to an extent comparable to PGC-1α-a. It was also shown that overexpression of PGC-1α-b or PGC-1α-c in skeletal muscle preferentially upregulated genes involved in mitochondrial biogenesis and fatty acid oxidation . Low-, medium-, and high-intensity exercise and AICAR injection increased PGC-1α-b and PGC-1α-c transcripts via β2-AR activation, whereas high-intensity exercise or AICAR injection increased PGC-1α-a transcripts independently of β2-AR activation .
Our previous studies have shown that alternative splicing between exons 6 and 7 of the PGC-1α gene produces an additional transcript encoding the N-terminal isoform of PGC-1α (NT-PGC-1α), which consists of 267 amino acids of PGC-1α and 3 amino acids from the splicing insert . NT-PGC-1α is a functional transcriptional coactivator since it retains the transcription activation and nuclear receptor interaction domains of PGC-1α [13–15]. In brown adipose tissue, three NT-PGC-1α mRNA isoforms (NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c) derived from exon 1a or exon 1b are coexpressed with three PGC-1α isoforms and regulate thermogenic and mitochondrial gene expression in response to cold stress .
In this study, we investigated isoform-specific expression of NT-PGC-1α mRNA in mouse skeletal muscle in response to different intensities of exercise, AMPK activator AICAR, and β2-adrenergic receptor agonist clenbuterol. We reported here that NT-PGC-1α-a mRNA is induced only by high-intensity exercise and AICAR, whereas NT-PGC-1α-b and NT-PGC-1α-c mRNAs are induced by low-to-high-intensity exercise, AICAR, and clenbuterol. Moreover, ectopic expression of NT-PGC-1α-a activates the muscle transcription program in cultured myotube cells, enhancing mitochondrial oxidative capacity.
2. Materials and Methods
2.1. Experimental Animals
Six-week-old male C57BL/6J (18–22 g) mice were obtained from SLAC LABORATORY ANIMAL (Shanghai, China). Mice were acclimated for 1 week in a light-controlled room (12 : 12 h light-dark cycle) under a constant temperature (22°C); standard mouse chow and water were available ad libitum. All experiments were approved by the Institutional Animal Care and Use Committee at China Pharmaceutical University and adhere to the Jiangsu Provincial Guidelines for the use of experimental animals.
2.2. Experimental Protocols
For running exercise experiments, mice were subjected to treadmill running at different intensity exercise, 10 m/min (low-intensity), 20 m/min (medium-intensity), and 30 m/min (high-intensity), for 30 min. Skeletal muscles (gastrocnemius) were isolated at 2 h after exercise [9, 17, 18]. For AICAR experiments, mice were injected with 250 mg/kg bw AICAR (i.p.) or the same volume of saline for control group. Skeletal muscles (gastrocnemius) were isolated at 3 h after AICAR injection [11, 19]. For β2-agonist experiments, mice were injected subcutaneously with 1 mg/kg bw clenbuterol (Sigma, USA) or the same volume of saline for control group. Skeletal muscles (gastrocnemius) were isolated at 4 h after clenbuterol injection [4, 9, 11]. In all experiments, skeletal muscle (gastrocnemius) was rapidly removed from mice killed by decapitation, frozen immediately in liquid nitrogen, and kept at −80°C until use.
2.3. Cell Culture and Transient Transfections
The C2C12 muscle cells were cultured in Dulbecco’s modified Eagle’s medium (Gibco, USA) supplemented with 10% fetal bovine serum and penicillin (100 U/mL)/streptomycin (100 μg/mL). When cells reached 80% confluence in six-well plates, they were switched to DMEM containing 2% heat-inactivated horse serum and pen/strep antibiotics for 3 days and differentiated to mature myotube cells. The differentiated cells were treated with AICAR (10−5 M) and clenbuterol (10−5 M) for 3 h and 1 h, respectively [9, 11, 20]. C2C12 myotube cells in six-well plate were transiently transfected with 2.0 μg of NT-PGC-1α-a/pcDNA3.1 plasmids per well for 24 h using X-tremeGENE HP DNA transfection reagent (Roche, Germany). Then, cells were washed with phosphate-buffered saline and collected and frozen at −80°C until they were assayed.
2.4. RNA Isolation and Real-Time PCR (RT-PCR) Assay
Total RNA was extracted from mouse skeletal muscle (gastrocnemius) or C2C12 cells using TRIzol reagent (Invitrogen, USA). According to the manufacturer’s protocol, 50–100 mg of skeletal muscle was mixed with 1 mL of TRIzol and homogenized using Homogenizer (IKA-T-10, Germany). The cells in a well of 6-well plate were mixed with 1 mL of TRIzol. RNA was separated from protein and DNA by the addition of chloroform and precipitated in equal volume of cold pure isopropanol. After a 75% ethanol wash and resuspension in 20 μL of DEPC-treated ddH2O, RNA samples were quantified by spectrophotometry. 1 μg of total RNA was reverse-transcribed using Oligo-(dT)18 primers and M-MLV reverse transcriptase (Roche, Germany) according to the protocol of First Strand cDNA Synthesis Kit (Roche, Germany) and 50 ng of cDNA was used as template for quantitative RT-PCR on Step One Plus System (Applied Biosystems, USA). The sequences of primers specific for PGC-1α-a, PGC-1α-b, and PGC-1α-c and NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c were designed (Figure 1(d)) and listed in Table 1. RT-PCR reactions were carried out in a 20 μL volume containing 1XFast Start Universal SYBR Green Master (ROX) (Roche, Germany), 50 ng cDNA, 0.3 μM forward and reverse primers (each). qRT-PCR reaction conditions for long products (~800 bp) were 95°C for 10 min and then 40 cycles of 95°C for 15 s, 60°C for 30 s, and 72°C for 1 min [21, 22]. Target gene expression in each sample was normalized to the endogenous control gene cyclophilin. The relative expression among the different conditions (exercise or treatment groups) was determined using the ΔΔ method as outlined in the Applied Biosystems protocol for RT-PCR.
|PGC-1: peroxisome proliferators-activated receptor- coactivator-1; NT-PGC-1: N-truncated PGC-1; Glut4: glucose transporter 4; ATP5B: ATP synthase B subunit; Cyc1: cytochrome C unit 1; COX5B: cytochrome oxidase 5 B subunit; MHC I: myosin heavy chain I; MHC II a: myosin heavy chain II a; MHC II b: myosin heavy chain II b; MHC II x: myosin heavy chain II x; Cyclophilin B: peptidylprolyl isomerase B; IFG-1: insulin-like growth factor 1.|
2.5. Western Blot Analysis
C2C12 cells were homogenized and sonicated in ice-cold lysis buffer (RIPA) containing 50 mM Tris/HCl (pH 7.4), 150 mM NaCl, 1% SDS, 0.1% Triton X-100, 0.5% sodium deoxycholate, and protease inhibitor cocktail (Roche, Switzerland). Cell lysates were centrifuged at 12,000 ×g, supernatant was collected, and protein concentration was determined with bicinchoninic acid (BCA) method. Equal amounts of total protein (100 μg) were loaded on 10% polyacrylamide gel (29 : 1 acrylamide-bisacrylamide), separated by SDS-PAGE, and transferred to PVDF membranes (Millipore, USA). The membrane was blocked for 1 h at room temperature in TBST buffer (50 mM Tris/HCl, 150 mM NaCl (pH 7.4), and 0.1% Tween-20) containing 5% nonfat dried milk. The membrane was incubated with the appropriate primary antibody in TBST with 5% nonfat dried milk overnight at 4°C. Primary antibody anti-PGC-1α mouse mAb (ST1202) (Calbiochem, USA) andanti-PGC-1α rabbit polyclonal antibody (SC-13067) (Santa Cruz, USA) were used to detect total NT-PGC-1α due to the commercial antibody against the same N-terminal sequence of PGC-1α and NT-PGC-1α. The antibody can only detect total PGC-1α and NT-PGC-1α but cannot distinguish each isoform of PGC-1α and NT-PGC-1α. Immunoblots were hybridized with antibody raised against β-tubulin (Santa Cruz, USA) as loading control. The membrane was then washed 3 times with TBST and incubated for 1 h with HRP-conjugated secondary antibody. Finally, the immunoreactive proteins were visualized using chemiluminescence reagent (Amersham Biosciences, USA).
2.6. Citrate Synthase (CS) Assay
Citrate synthase activity was determined using a commercially available kit (Genmed, China). The principle of the assay is the reaction of acetyl-CoA with OAA (oxaloacetate) and the release of free CoA-SH, which reacts with a colorimetric reagent, DTNB [5,5-dithiobis(2-nitrobenzoate)], to form yellow colored compound (5-thio-2-nitrobenzoic acid (TNB)) . The procedures were applied based on the manufacture’s guideline. Briefly, C2C12 myotube cells transfected with NT-PGC-1α-a/pcDNA3.1 were collected and lysed to disrupt the mitochondria and expose the CS. The supernatants were collected by centrifugation at 16,000 g for 5 min at 4°C. The protein concentration was measured by BCA method. 10 μL (20 μg) of total protein containing CS was added to test well containing reaction substrates reagent and 10 μL of negative control reagent was added to control well. The formation of 5-thio-2-nitrobenzoic acid was measured spectrophotometrically at 412 nm in 96-well format by using a microplate reader (Bio-TeK, USA) at 0 min and 15 min. All measurements were performed in duplicate in the same setting at 20–22°C. The CS activity was then normalized to the total protein content and was reported in as nanomoles per milligram protein per minute.
2.7. Statistical Analysis
Values are expressed as means ± S.E. Statistically significant differences were determined using unpaired Student’s -tests. Statistical differences were considered significant if .
3.1. Expression and Identification of NT-PGC-1α and PGC-1α Isoforms in Mouse Skeletal Muscle
Three PGC-1α isoforms, PGC-1α-a, PGC-1α-b, and PGC-1α-c, which are derived from either exon 1a or exon 1b, have been reported in skeletal muscle [9, 10]. In addition, the expressions of NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c isoforms have been reported in brown adipose tissue . They all arise from different promoter usage and alternative internal splicing (Figures 1(a), 1(b), and 1(c)). Thus, these previous studies suggest that the single PGC-1α gene can produce six different transcripts in skeletal muscle. To explore the isoform-specific expression of NT-PGC-1α mRNA in skeletal muscle, specific primers (Table 1) were designed to detect only NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c mRNA as described in Figure 1(d). In addition, we designed a set of primers that detect only PGC-1α-a, PGC-1α-b, and PGC-1α-c mRNA (Figure 1(d)). The expression levels of NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c and PGC-1α-a, PGC-1α-b, and PGC-1α-c can be quantitatively determined by qRT-PCR. The slopes of the resulting standard curves relating log mass of NT-PGC-1α-a, NT-PGC-1α-b, NT-PGC-1α-c, PGC-1α-a, PGC-1α-b, and PGC-1α-c cDNA to cycle threshold are −3.968, −3.787, −3.748, −3.619, −3.837, and 3.868 (Figure 1(e)). Each PCR product amplified by a specific set of primers was checked by agarose gel analysis (Figure 1(f)) and the specificity of PCR products was confirmed by DNA sequencing (data not shown).
3.2. Exercise Intensity-Dependent Expression of NT-PGC-1α mRNA Isoforms in Skeletal Muscle
To examine whether the expression of NT-PGC-1α mRNA isoforms is differentially induced in skeletal muscle in response to different intensities of exercise, C57BL/6J mice were subjected to treadmill running exercise at different intensities, 10 m/min (low-intensity), 20 m/min (medium-intensity), and 30 m/min (high-intensity), for 30 min according to the exercise program. Basal mRNA levels of NT-PGC-1α-b and NT-PGC-1α-c were very low when compared with that of NT-PGC-1α-a in control mice (Figure 2(a)). At low- and medium-intensity exercise, expression of NT-PGC-1α-a mRNA was not altered, but expression of NT-PGC-1α-b and NT-PGC-1α-c mRNA was significantly elevated (Figure 2(a)). After high-intensity exercise, NT-PGC-1α-b and NT-PGC-1α-c mRNA showed 97-fold and 28-fold increases in expression, respectively, whereas NT-PGC-1α-a mRNA levels increased by 2.1-fold (Figure 2(a)). It has been reported that a single exercise bout resulted in an increment in PGC-1 protein concentration . In this study, we found that total NT-PGC-1α protein is a constitutive expression in skeletal muscle and is also increased by exercise (Figure 2(b)). In parallel, PGC-1α mRNA isoforms had a similar isoform-specific expression pattern in response to different intensities of exercise (Figure 2(c)). Taken together, these data illustrate that three NT-PGC-1α transcripts are coexpressed with PGC-1α isoforms in mouse skeletal muscle, but their relative expression levels are dependent on exercise intensity.
3.3. AMPK Activator AICAR Increases the Expression of Three NT-PGC-1α mRNAs in Skeletal Muscle
AICAR is a pharmacological activator of AMPK showing similar effects of exercise for increasing PGC-1α expression [11, 19], mitochondrial biogenesis, and fatty acid oxidation in skeletal muscle. To examine the effect of AMPK activation on isoform-specific expression of NT-PGC-1α mRNA in skeletal muscle, mice were injected i.p. with 250 mg/kg body weight AICAR or the same volume of saline. Skeletal muscles (gastrocnemius) were isolated after AICAR injection for 3 h, and gene expression was analyzed by qPCR. The expressions of NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c mRNA were increased by 2.2-fold, 3.2-fold, and 2.4-fold, respectively (Figure 3(a)). In addition, a similar increase in PGC-1α isoforms expression was observed (Figure 3(b)). These data illustrate that the proximal and alternative promoters are similarly activated by AMPK activation to produce exon 1a- and 1b-derived NT-PGC-1α and PGC-1α transcripts.
3.4. β2-AR Agonist Clenbuterol Increases the Expression of NT-PGC-1α-b and NT-PGC-1α-c but Not NT-PGC-1α-a in Skeletal Muscle
Given that β2-adrenergic receptor agonist clenbuterol increases PGC-1α expression in skeletal muscle [4, 9, 11], we examined the effect of clenbuterol on isoform-specific expression of NT-PGC-1α mRNA. β2-AR agonist clenbuterol was subcutaneously injected to C57BL/6J mice at a dose of 1 mg/kg body weight in our experiments. The expressions of NT-PGC-1α-b and NT-PGC-1α-c mRNA were significantly increased by clenbuterol, whereas there was no change in mRNA levels of NT-PGC-1α-a (Figure 4(a)). Similarly, PGC-1α-b and PGC-1α-c mRNAs, but not PGC-1α-a mRNA, were largely induced by clenbuterol in skeletal muscle (Figure 4(b)), indicating that the alternative promoter of the PGC-1α gene is more responsive to β2-AR signaling.
3.5. NT-PGC-1α-a Enhances Mitochondrial Oxidative Function in C2C12 Myotube Cells
A recent study reported a muscle-specific PGC-1α isoform, PGC-1α4, which has shown to be induced by resistance training . PGC-1α4 is actually identical to NT-PGC-1α-b, which is derived from exon 1b of the PGC-1α gene. NT-PGC-1α-b (PGC-1α4) has shown to induce muscle cell hypertrophy but not mitochondrial biogenesis . Given that NT-PGC-1α-a is induced by exercise in mouse skeletal muscle, we explored whether NT-PGC-1α-a regulates the transcription program in skeletal muscle. To test NT-PGC-1α-a function, differentiated C2C12 cells were used as a myotube cell model since no detectable NT-PGC-1α-a mRNA (data not shown) and protein (Figure 5(a)) were observed in differentiated C2C12 cells even after treatment with either AICAR or clenbuterol. Thus, overexpression of exogenous NT-PGC-1α-a was carried out by transfection of differentiated C2C12 cells with NT-PGC-1α-a (Figure 5(b)).
There are four muscle fiber types, Type I, Type II a, Type II b, and Type II x, which can be distinguished by the type of myosin heavy chain (MHC) isoform(s) [25, 26]. Type I fibers are referred to as being “slow twitch oxidative.” Type II a fibers are “fast twitch oxidative.” Type II b fibers are “fast twitch glycolytic,” and Type II x fibers are intermediate to Type II a and II b fibers. Type I fibers have an oxidative profile with high mitochondrial content, capillary density, and glucose transporter 4 (Glut4) expression sensitive to insulin. We found that NT-PGC-1α-a promoted the expression of MHC I, MHC II a, and Glut4 in differentiated C2C12 cells by more than 30-fold, 20-fold, and 6-fold, respectively (Figure 6(a)), but decreased the expression of MHC II b and MHC II x by 60 percent and 70 percent (Figure 6(a)). These results indicate that NT-PGC-1α-a has a potential role in skeletal muscle adaptation to a more oxidative phenotype during endurance exercise.
IGF-1 plays an essential role in muscle development, muscle cell proliferation, and muscle growth . Myostatin is a negative regulator of muscle growth and functions by inhibiting myoblast proliferation . We found that NT-PGC-1α-a promoted the expression of IGF-1 in differentiated C2C12 cells by more than 1.5-fold (Figure 6(a)) but decreased the expression of myostatin by 70 percent (Figure 6(a)). These data demonstrated that NT-PGC-1α-a has a potential role in muscle development, muscle cell proliferation, and muscle growth.
To assess whether NT-PGC-1α-a expression alters mitochondrial biogenesis and function, several markers of mitochondrial biogenesis and function were examined in NT-PGC-1α-a-transfected C2C12 myotube cells. The mRNA expressions of mitochondrial component genes, Cyc1, COX5B, and ATP5B, were upregulated by 18.9-, 2-, and 1.5-fold, respectively, when compared with control C2C12 cells transfected by an empty vector pcDNA3.1 (; Figure 6(b)). These nuclear DNA-encoded mitochondrial proteins are critical for mitochondrial biogenesis and oxidative metabolism. Citrate synthase is one of the key regulatory enzymes in an energy-generating metabolic pathway . It has been extensively used as a metabolic marker for assessing mitochondrial oxidative capacity. The activity of citrate synthase in NT-PGC-1α-transfected C2C12 myotube cells was 1.4-fold higher than that of control C2C12 cells (Figure 6(c)). This is consistent with the studies reporting the acute increase in CS activity in skeletal muscle after a single bout of exercise .
The PGC-1α gene has been thought to produce single transcript and protein. However, recent studies reported that multiple mRNAs are produced from the PGC-1α gene by different exon usage and alternative splicing in skeletal muscle and brown adipose tissue [9, 10]. We show here that NT-PGC-1α-a, NT-PGC-1α-b, and NT-PGC-1α-c are coexpressed with PGC-1α-a, PGC-1α-b, and PGC-1α-c in mouse skeletal muscle. Consistent with the previous findings on PGC-1α expression in mouse skeletal muscle, isoform-specific expression of NT-PGC-1α mRNA was dependent on exercise intensity . Exon 1a-driven NT-PGC-1α-a was induced by both high-intensity exercise and AMPK activation but not by β2-AR stimulation, whereas expression of exon 1b-driven NT-PGC-1α-b and NT-PGC-1α-c were markedly elevated by low-to-high-intensity exercise, AICAR, and clenbuterol. Transcriptional shift between exon 1a and exon 1b of the PGC-1α gene may imply isoform-specific roles for NT-PGC-1α in basal and exercised conditions. The further studies on the underlying mechanism involving transcription factors on the proximal and alternative promoters and the physiological regulation of proximal and alternative promoters are warranted. In addition, it is also important to explore the molecular mechanism and regulation of the alternative splicing that produce NT-PGC-1α from posttranscription modification of PGC-1α pre-mRNA in different physiological and pathological conditions.
The exercise-inducible and exon 1b-driven NT-PGC-1α-b is actually identical to a recently identified muscle-specific PGC-1α isoform, PGC-1α4 . PGC-1α4 has shown to be induced by resistance training, but not by endurance training, and regulate skeletal muscle mass . However, we observed here that NT-PGC-1α-b expression is largely elevated by low-to-high endurance exercise, AMPK activation, and β2-AR activation in mouse skeletal muscle. In agreement with our findings, a recent study has reported that NT-PGC-1α-b (PGC-1α4) is induced by both endurance and resistance exercise in human skeletal muscle . Moreover, PGC-1α-b expression was largely elevated by endurance exercise, AMPK activation, and β2-AR activation in mouse skeletal muscle. Skeletal muscle-specific expression of PGC-1α-b has shown to increase mitochondrial biogenesis and exercise capacity [9, 29].
Type I fibers containing MHC I are referred to as being “slow twitch oxidative” and have an oxidative profile with high mitochondrial content, capillary density, and glucose transporter 4 (Glut4) expression sensitive to insulin. Type II a fibers expressing MHC II a are fatigue resistant and have the highest oxidative (aerobic) capacity of the fast fibers with numerous mitochondria. Type II b fibers are the fastest contracting and fatiguing fibers which contain Type MHC II b and few mitochondria, using primarily glycolytic (anaerobic) pathways to generate energy for contraction [25, 26]. Type I fibers are characterized by low force/power/speed production and high endurance, Type II b and Type II x fibers are characterized by high force/power/speed production and low endurance, while Type II a fibers fall in between . Here, we clearly showed that overexpression of NT-PGC-1α-a in cultured C2C12 myotubes upregulates the expression of myosin heavy chain I and II a (MHC I, MHC II a), glucose transporter 4 (Glut4), and insulin-like growth factor 1 (IGF-1), while reducing MHC II b, MHC II x, and myostatin mRNA expression. Furthermore, NT-PGC-1α-a induced the expression of mitochondrial respiratory subunit (COX5B, Cyc1, and ATP5B) and increased the mitochondrial oxidative enzyme CS activities. However, NT-PGC-1α-b (PGC-1α4) and PGC-1β have shown to induce the expression of MHC II x, but not MHC I, in skeletal muscle [17, 30]. Furthermore, NT-PGC-1α-b (PGC-1α4) has shown to promote muscle development, muscle cell proliferation, and muscle growth . These data suggested that NT-PGC-1α-a promotes muscle fiber switching to more oxidative phenotype in gastrocnemius with increased mitochondrial biogenesis and muscle growth. The presence and differential expression of multiple PGC-1α and NT PGC-1α isoforms may enhance the ability of skeletal muscle to optimally adapt to different intensities of exercise.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Xingyuan Wen and Jing Wu contributed equally to this work.
This work was supported by the National Natural Science Foundation of China Grant 81072679 to Yubin Zhang; Opening Project of Shanghai Key Laboratory of Complex Prescription, Shanghai University of T.C.M. (11DZ2272300); and a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD); and COBRE Grant NIH8 P20-GM103528 to Ji Suk Chang and Thomas W. Gettys.
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