Involvement of adiponectin in the pathogenesis of dystrophinopathy
Skeletal Muscle volume 5, Article number: 25 (2015)
The hormone adiponectin (ApN) is decreased in the metabolic syndrome, where it plays a key pathogenic role. ApN also exerts some anti-inflammatory effects on skeletal muscles in mice exposed to acute or chronic inflammation. Here, we investigate whether ApN could be sufficiently potent to counteract a severe degenerative muscle disease, with an inflammatory component such as Duchenne muscular dystrophy (DMD).
Mdx mice (a DMD model caused by dystrophin mutation) were crossed with mice overexpressing ApN in order to generate mdx-ApN mice; only littermates were used. Different markers of inflammation/oxidative stress and components of signaling pathways were studied. Global force was assessed by in vivo functional tests, and muscle injury with Evans Blue Dye (EBD). Eventually, primary cultures of human myotubes were used.
Circulating ApN was markedly diminished in mdx mice. Replenishment of ApN strikingly reduced muscle inflammation, oxidative stress, and enhanced the expression of myogenic differentiation markers along with that of utrophin A (a dystrophin analog) in mdx-ApN mice. Accordingly, mdx-ApN mice exhibited higher global force and endurance as well as decreased muscle damage as quantified by curtailed extravasation of EBD in myofibers. These beneficial effects of ApN were recapitulated in human myotubes. ApN mediates its protection via the adiponectin receptor 1 (AdipoR1, the main ApN receptor in muscle) and the AMPK-SIRT1-PGC-1α signaling pathway, leading to downregulation of the nuclear factor kappa B (NF-κB) and inflammatory genes, together with upregulation of utrophin.
Adiponectin proves to be an extremely powerful hormone capable of protecting the skeletal muscle against inflammation and injury, thereby offering novel therapeutic perspectives for dystrophinopathies.
Adiponectin (ApN) is a hormone abundantly secreted by adipocytes; its circulating levels are decreased in obesity and in patients meeting the criteria for the metabolic syndrome. ApN can exhibit insulin-sensitizing, fat-burning, and anti-inflammatory properties as well as modulatory effects on oxidative stress , thereby thwarting simultaneously several facets of this syndrome .
Adiponectin receptors 1 and 2 (AdipoR1 and AdipoR2) serve as major receptors for ApN by activating the AMP-activated protein kinase (AMPK) and peroxisome proliferator-activated receptor alpha (PPARα) pathways, respectively. AdipoR1 is abundantly expressed in skeletal muscle, whereas AdipoR2 is predominantly expressed in the liver . Skeletal muscle is a major target tissue of ApN. Injection of recombinant ApN to mice or more chronic elevation of ApN in transgenic mice clearly demonstrate the potent insulin-sensitizing properties of the molecule in vivo . ApN also enhances muscle fatty acid consumption . Conversely, muscles of ApN-deficient mice were insulin-resistant  and displayed higher susceptibility to oxidative stress, inflammation, and apoptosis; all these abnormalities were exacerbated by acute or chronic inflammatory challenge and corrected by local electrotransfer of the ApN gene [6, 7]. Mice with muscle-specific disruption of AdipoR1 also showed muscle insulin resistance, decreased exercise capacity, mitochondrial content, and oxidative metabolism, as well as enhanced oxidative stress . The presence/action of ApN is therefore important not only to regulate muscle fuel partitioning/metabolism but also to counterbalance inflammation or cellular stress in this organ [6, 7].
Duchenne muscular dystrophy (DMD) is the most frequently inherited human myopathy and the most devastating type of muscular dystrophy. DMD stems from X-linked recessive defects in the gene encoding for dystrophin, a key scaffolding protein of the dystroglycan complex [9, 10]. This complex connects the actin cytoskeleton of myofibers to the extracellular matrix and is thus crucial for maintaining cell membrane stability/permeability as well as normal contractile function of the skeletal muscle. Disruption of this complex leads to membrane damage allowing massive infiltration of immune cells, chronic inflammation, necrosis, and severe muscle degeneration . Normally, muscle cells possess the capacity to regenerate in response to injury signals. However, this ability is progressively lost in DMD, due to an exhaustion of satellite cells during ongoing degeneration/regeneration cycles . Although dystrophin mutations represent the primary cause of DMD, it is the secondary processes involving persistent inflammation and subsequent impaired regeneration that likely exacerbate disease progression .
The aim of this work was to explore whether ApN may play a beneficial role in DMD. To this end, dystrophin-deficient mdx mice, a widely used mouse model of DMD, were crossed with our transgenic mice, which moderately overexpress ApN . These transgenic mice with homotopic overexpression of native ApN showed a moderate elevation of circulating ApN with no change in the distribution of ApN multimers . We thus examined whether the resulting mdx-ApN mice exhibited a lower degree of muscle inflammation, oxidative stress, and injury together with improved muscular function. Lastly, we unraveled the mechanisms underlying the protection afforded by ApN.
Transgenic C57BL/6J mice overexpressing adiponectin (ApN mice), which had been generated in our lab, were used; native full-length ApN was placed under the control of the adipocyte aP2 promoter, thereby targeting ApN expression to white adipose tissue. As ApN is secreted, these mice also showed a moderate elevation of circulating ApN levels . C57BL/10ScSn mdx mice were purchased from Jackson Laboratory (Maine, USA) and crossed with ApN mice in order to obtain mdx mice overexpressing ApN (mdx-ApN mice). Three groups of F1 mice were studied in all experiments: the mdx-ApN mice, their mdx littermates (true controls), and wild-type (WT) mice; the three groups of mice were maintained on the same C57BL/6J-10 ScSn genetic background. Only male mice were studied.
These animals were maintained under a standard laboratory chow and housed at a constant temperature with a fixed light-dark cycle. At the end of the experiments, mice were sacrificed by cervical dislocation (between 09.00 and 11.00 h). Blood samples were saved. Pairs of tibialis anterior (TA) muscles or inguinal fat pads were weighed, frozen in liquid nitrogen, and stored at −80 °C for subsequent analyses. For some experiments dealing with evaluation of muscle injury, additional muscles were sampled.
All procedures were approved by the Ethical Committee for Animal Experimentation from the Medical Sector at the Catholic University of Louvain.
Light microscopy, immunohistochemistry, and morphometry
Muscle samples were fixed in 10 % formalin for 24 h and embedded in paraffin. Sections 5 μm thick were stained with hematoxylin-erythrosin-safran (HES). The percentage of muscle fibers with central nuclei (a characteristic feature of DMD) was determined on more than 1000 fibers per muscle section. For immunohistochemistry, sections were processed as previously described  using rabbit polyclonal antibodies directed against peroxiredoxin 3 (PRDX3, dilution 1:700, incubation 2 h), peroxiredoxin 5 (PRDX5, 1:300, 2 h) [gifts from B. Knoops, University of Louvain, Brussels, Belgium ], 4-hydroxy-2-nonenal (HNE, 1:100, 2 h), tumor necrosis factor alpha (TNFα, 1:200, 2 h), interleukin-1β (IL-1β, 1:300, overnight), and nuclear factor kappa B (NF-κB, 1:50, overnight) (all from Abcam, Cambridge, UK). Rat monoclonal antibodies directed against markers of macrophages (CD68) or of T lymphocytes (CD3) (1:50, overnight, Abcam) were also used. Before immunostaining, sections were submitted to heat-mediated antigen retrieval using a microwave oven and Tris-citrate buffer (pH 6.5). Binding of antibodies was detected by applying for 30 min at room temperature a second antibody, which was a biotinylated goat anti-rabbit IgG (H+L) or a biotinylated rabbit anti-rat IgG (H+L) (Labconsult, Brussels, Belgium). Peroxidase activity was revealed with 3,3′-diaminobenzidine (DAB) (Life Technologies, Gent, Belgium), which produces a brown staining. For each marker, all slides from the three groups of mice were treated simultaneously for immunohistochemistry analysis and DAB revelation, and then analyzed together. Immunohistochemical controls were performed by omission of the first antibody or of the first and second antibodies or by using pre-immune serum. For quantification of NF-κB expression, the percentage of immunolabeled nuclei was determined after counting an average of 1000 fiber nuclei per slide for each mouse. For PRDX3/5, HNE, TNFα, IL-1β, CD3, and CD68, whole muscle section were scanned using the Leica SCN400 slide scanner (Leica Microsystems, Diegem, Belgium), and then the percentage of DAB surface area within muscle fibers was quantified using the Tissue Image Analysis 2.0 (Leica).
In vivo studies of global force or resistance
Mice were submitted to three main tests:
Wire test. Animals were suspended by their forelimbs from a 1.5 mm-thick, 60 cm-long metallic wire at 45 cm above soft ground. The time (seconds) until the mouse completely released its grasp and fell down was recorded. Three trials were performed per session, with a 30-s recovery period between trials. The maximum time per trial was set to 180 s. For each mouse, the scores of the three trials were averaged .
Grip test. The grip strength test measures the muscle strength of forelimb or of combined fore- and hindlimb muscles. Limb strength was recorded using a grid connected to a sensor (Panlab-Bioseb, Vitrolles, France). The mice were gently laid on the top of the grid so that their front paws (forelimb test) or both fore and hind paws (combined test) can grip the grid. Then, mice were pulled back steadily until the grip was released down the complete length of the grid. Each test was repeated three times at an interval of 20 min. Results are presented as the mean of the two highest values of force recorded, related to body weight .
A third test of eccentric exercise was also performed mainly to evaluate muscle injury (see below).
Quantification of muscle damage markers in plasma
Plasma creatine kinase (CK) and lactate dehydrogenase (LDH) activities were quantified to evaluate skeletal muscle damage as injured muscles release CK and LDH into the bloodstream at high levels. Kits were based on colorimetric methods (Gentaur, Kampenhout, Belgium). CK and LDH activities were expressed as IU/L.
Evaluation of muscle injury after in vivo staining with Evans blue dye
Evans blue dye (EBD) irreversibly binds to plasma albumin in vivo, and upon injury, the complex leaks into the surrounding tissues [16, 17]. EBD (Sigma-Aldrich, Bornem, Belgium) was dissolved in PBS buffer, sterilized by filtration through membrane with pore size of 0.2 μm, and kept at 4 °C. The dye solution was injected ip into the mice (1 mg dye/0.1 ml/10 g body weight). The mice were sacrificed 24 h later either in basal (sedentary) conditions or after bouts of eccentric exercise .
Eccentric exercise. The mice were subjected to a downhill running exercise on a treadmill with a downward inclination of 15°, and at a speed of 10 m/min for 10 min. This training was repeated daily for 3 days, and the mice were sacrificed 1 h after the 3rd session and 24 h after the EBD injection . Six different muscles were studied: biceps brachii (BB) and triceps brachii (TB) from the forelimbs; TA, gastrocnemius (G), extensor digitorium longus (EDL), and soleus (S) from the hindlimbs.
Spectrophotometric detection of EBD. EBD was extracted from powdered muscle using dimethylformamide, and the absorbance was read spectrophotometrically at 620 nm. The extravasated EBD concentration was calculated against a standard curve and was expressed as ng of EBD/mg muscle weight .
Fluorescence microscopy detection of EBD. Muscles were embedded in Tissue-Tek (Sakura, Alphen-aan-den-Rijn, Netherlands) using iso-pentane frozen in liquid nitrogen. Three different transverse cryostat sections (10 μm thick) were obtained for each muscle and observed by fluorescence microscopy .
Western blotting and immunoprecipitation
Skeletal muscle was homogenized in a lysis buffer (Cell Signaling Technology, BIOKE, Leiden, The Netherlands) supplemented with 100 mM NaF and 1 % protease inhibitor cocktail (Active Motif, Rixensart, Belgium). Immunoblotting was performed as reported  by using rabbit polyclonal antibodies directed against phospho-NF-κB p65 (phosphor Ser536) and myogenic factor 5 (Myf5) (both from Abcam); AMPK, P-AMPK, and Sirtuin 1 (SIRT1) (all form Cell Signaling); peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) and Utrophin (both from Santa Cruz, Heidelberg, Germany); or a mouse monoclonal antibody directed against myogenic differentiation (MyoD) (Abcam). Signals were revealed by enhanced chemiluminescence, then quantified and normalized to those of actin, Ponceau stain or the studied protein without post-translational modifications (when these modifications were studied) using ImageJ program (National Institutes of Health, Maryland, USA).
To obtain protein extracts for immunoprecipitation, skeletal muscle was homogenized in the lysis buffer indicated above, supplemented with 1 % protease/phosphatase inhibitor cocktail (Cell Signaling), 5 mM nicotinamide, and 1 mM sodium butyrate. A total of 1000 mg of proteins from muscle samples were used. The immunoprecipitation was carried out using magnetic beads (Thermo Fisher Scientific, Lafayette, CO) and anti-PGC-1α antibody (2 μl antibody/1 g total protein; Santa Cruz) following the manufacturer’s instructions. The beads were collected using neodymium magnets and washed with TBS-Tween 0.05 %. After the final wash, the samples were dissolved in 100 μl of elution solution (0.1 M glycine, pH 2.5); 20 μl were then separated by SDS-PAGE and immunoblotted, as described , using an acetyl-lysine antibody (1:1.000; Cell Signaling) and anti-PGC-1α antibody (1:1.000; Santa Cruz), respectively.
Culture of human myotubes
Primary cultures of human skeletal muscle cells were initiated from satellite cells of quadriceps samples obtained from male organ donors (n = 5, 40 ± 9 years) or from latissimus dorsi flap samples obtained from women undergoing reconstructive surgery after breast cancer (n = 6, 48 ± 13 years). The last series of biopsy samples were used for siRNA transfection experiments. For each patient, the culture experiments were done in duplicate and the data from a given individual were then averaged. Patients provided written informed consent, and the study protocol had the approval of the local Ethical Committee of Saint-Luc University Hospital.
Cultures were performed as described  with minor modifications. Myoblasts were grown in 35-mm (or 6 wells; siRNA transfection) plates at 37 °C in the presence of 5 % CO2 in F-12 (Ham) supplemented with 12 % fetal bovin serum (FBS), 1 % l-glutamine, and 100 μg/ml Primocin™ (Invivogen, Toulouse, France) (all other products from Life Technologies, Inc., Merelbeke, Belgium). After 3–5 days of proliferation, at the end of which the seeding density has reached 70–80 %, the growth medium was replaced by the fusion medium which consists of 1 part DMEM, 1 part F-12 (Ham), 2 % horse serum (HS), 1 % l-glutamine, and 1 % penicillin-streptomycin (Life Technologies). This fusion medium was then changed every 2 days, and differentiation was allowed to continue for 10 days (time required to obtain mature myotubes with characteristic elongated and multinucleated morphology) before the experimentation period.
Ten days after differentiation, cells were treated with human recombinant TNFα (10 ng/ml) + interferon gamma (IFNγ) (10 ng/ml) and/or ApN (5 μg/ml), at the indicated concentrations, for 24 h (TNFα from Tebu-Bio, Boechout, Belgium, IFNγ from R&D systems, Abington, UK, and ApN from Biovendor, Heidelberg, Germany). In some experiments, cells were first transfected before inflammatory challenge and/or ApN treatment. Briefly, 3.105 cells/well were transfected with either the On-Targetplus non-targeting pool siRNAs (negative control, NT siRNAs), or a specific On-Targetplus siRNA SMARTpool against human AdipoR1 (50 nM) or human SIRT1 (50 nM) or human PGC-1α (70 nM) (all from Dharmacon, Thermo Fisher Scientific) using 7 μl Lipofectamine RNAiMAX reagent (Life Technologies) for 24 h. siRNA silencing was effective, ranging from 70 to 95 % in all experiments. Next, the medium was renewed and cells were treated with TNFα + IFNγ with or without ApN for an additional 24 h. At the end of the experiments, cells were collected and rinsed twice in PBS before RNA extraction.
RNA extraction and real-time quantitative PCR (RT-qPCR)
RNA was isolated from cultured cells and from mouse adipose tissue with TriPure reagent (Roche Diagnostics, Vilvoorde, Belgium). Of the total RNA, 1–2 μg were reverse transcribed, as described previously . RT-qPCR primers were designed for mouse cyclophilin, ApN as reported , for interleukin 10 (IL-10; sense, 5′-TGA TGC CCC AGG CAG AGA AGC A-3′; antisense, 3′-GGG GAG AAA TCG ATG ACA GCG CCT C-5′), myosin heavy chain 7 (Myh7; sense, 5′-GGT GCC AAG GGC CTG AAT GAG GAG-3′; antisense, 3′-GGT CTG AGG GCT TCA CGG GCA C-5′), myosin heavy chain 1 (Myh1; sense, 5′-AGC TTC AAG TTT GGA CCC ACG GTC G-3′; antisense, 3′-GCA GCC TCC CCG AAA ACG GC-5′), myosin heavy chain 6 (Myh6/Mrf4; sense, 5′-TGC GGA TTT CCT GCG CAC CT-3′; antisense, 3′-GCA TCC ACG TTT GCT CCT CCT TCC-5′), myosin heavy chain 3 (Myh3/eMyHC; sense, 5′-CAG AAA TGG AGA CAC GGA TCA GA-3′; antisense, 3′-AGA GGT GAA GTC ACG GGT CTT TGC C-5′), myogenin (MyoG; sense, 5′-CCA GCC CAT GGT GCC CAG TGA A-3′; antisense, 3′-TGT AGG GTC AGC CGC GAG CAA-5′), and utrophin A (sense, 5′-GCC AGA CAC TAT GAC CCC TCC CA-3′; antisense, 3′-GGG CAT GCT CAT CCT CCA CGC T-5′). RT-qPCR primers for human TATA box-binding protein (TBP), TNFα, interleukin-6 (IL-6) were similar to those previously reported , for IκB (sense, 5′-TGT GGC AAC TGG AAG CAA GCC C-3′; antisense, 3′-ACC ATG GCC GCA TCA ATG TGC T-5′), and utrophin A (sense, 5′-AGT TCC ACC AGG CAG CGG GAG-3′; antisense, 3′-ACC TCC GTG AGA TCC GTG CTG G-5′). Cyclophilin (mouse) and TBP (human) were used as reporter genes. Of the total RNA equivalents, 40–80 ng were amplified using an iCycler iQ real-time PCR detection system (Bio-Rad Laboratories, Nazareth, Belgium) . The threshold cycles (Ct) were measured in separate tubes and in duplicate. The identity and purity of the amplified product were checked by electrophoresis on agarose minigels, and analysis of the melting curve was carried out at the end of the amplification. To ensure the quality of the measurements, each plate included a negative control for each set of primers.
Result presentation and statistical analysis
Results are means ± SD for the indicated number of mice or experiments. Comparisons between the three groups of mice (WT, mdx, and mdx-ApN) were carried out by one-way ANOVA followed by Tukey’s test (Prism 5; GraphPad Software, California, USA). When more than three experimental conditions were compared in vitro, the influence of ApN and that of TNFα/IFNγ were assessed by two-way ANOVA with F test, followed by post hoc two by two comparisons with Bonferroni correction for multiple comparisons (Prism 5). Comparisons between two myotubes conditions from a given subject were made using two-tailed paired Student’s t test. Differences were considered statistically significant at P < 0.05.
Characteristics of mdx mice overexpressing adiponectin
Because skeletal muscle of mdx mice exhibit degenerative-regenerative cycles between 2 and 14 weeks of age, we chose mid-stage mice for most experiments . We thus compared three groups of 8-week-old mice: the mdx mice overexpressing ApN, their mdx littermates (true controls), and WT mice (Table 1).
There were no significant differences in body weight between any groups. However, as expected , mdx mice presented an increase in tibialis anterior mass, which was corrected in mdx-ApN mice (Table 1).
Remarkably, circulating ApN was decreased by ~40 % in mdx mice compared to WT mice. This decrease was explained by halved expression of ApN in fat tissue, the major contributor to systemic levels. Compared to mdx controls, plasma ApN was increased in mdx-ApN mice (and was almost completely normalized), in line with the 3-fold rise of ApN mRNAs in adipose tissue, where the transgene under the control of the adipocyte aP2 promoter is overexpressed (Table 1) .
Effects of adiponectin on markers of inflammation and oxidative stress in mdx muscles
We tested the hypothesis that ApN replenishment could slow down the progression of dystrophic pathology by counteracting excessive inflammation/oxidative reactions.
When compared to WT mice, myofibers from tibialis anterior of mdx mice displayed a strong immunolabeling for PRDX3/5, two markers of oxidative stress, and for HNE, a lipid peroxidation product (Fig. 1). Quantification of this immunolabeling showed that the extent of DAB staining within myofibers was ~7.5- to 9.5-fold higher in mdx than in WT mice (see Fig. 2a–c). Qualitatively similar results were observed for TNFα and for IL-1β, two pro-inflammatory cytokines (Fig. 1), with an extent of DAB staining being 11- and 6-fold greater in mdx than in WT mice, respectively (Fig. 2d, e). In addition, a massive infiltration of both T lymphocytes (immunolabeling for CD3) and macrophages (CD68, a marker of the pro-inflammatory M1 phenotype; ) was observed in mdx mice, but not in WT mice (Fig. 1 and Fig. 2f, g). All these indicators of oxidative stress and inflammation were remarkably reduced in mdx-ApN mice (Figs. 1 and 2). Serial muscle cross-sections revealed that both myocytes and macrophages contribute to the production of pro-inflammatory cytokines. In mdx mice, areas that were positive for C68 were negative for TNFα, while this cytokine was abundant within the myocytes. A reverse pattern of expression was however observed for IL-1β, which was mainly produced by macrophages and less by myocytes (Fig. 3). Remarkably, gene expression of IL-10, an anti-inflammatory cytokine that activates the M2 macrophage phenotype  was also markedly increased in mdx-ApN mice (Fig. 2h). Taken together, these data suggest that ApN is able to strongly defend the skeletal muscle against excessive inflammatory reactions and oxidative stress.
This effect of ApN persisted later in life. In 1-year-old mice, oxidative stress and inflammation were still blunted in mdx-ApN muscles, as shown by reduced expression of HNE and TNFα (Additional file 1: Figure S1).
Effects of adiponectin on markers of muscle differentiation in mdx mice
Since ApN has been found to induce myogenesis in C2C12 cells , we explored different key markers involved in the skeletal myogenic program . The expression of MyoD and Myf5 proteins, that activate satellite cells to proliferate , was markedly reduced in tibialis anterior of mdx mice when compared to WT mice (-80 and −60 %, respectively). The decrease of these proliferation markers, which may be ascribed to the inflammatory context [27, 28], was partially restored in mdx-ApN mice (Fig. 4a, b). Two later markers (early differentiation phase), myogenin and Mrf4, were next studied. Mrf4 showed a pattern of expression similar to that of the proliferation markers, while myogenin was increased in mdx mice and further upregulated in mdx-ApN ones (Fig. 4c, d). The regeneration marker, the embryonic myosin heavy chain (Myh3) behaved similarly (Fig. 4e).
The proportion of fibers with central nuclei, a hallmark of dystrophic muscle, was almost undetectable in WT mice (<1 %), amounted to 64 % in mdx mice, and was reduced to 49 % in mdx-ApN mice (Fig. 4f, g). This reduction suggests improved myogenic program and more complete muscle regeneration.
Effects of adiponectin on global force and resistance of mdx mice
We used two different functional tests to investigate in vivo the global muscular force: the wire test and the grip test. The wire test evaluates muscle force and resistance to fatigue: the mouse is suspended from a horizontal wire and the time until the mouse releases its grasp is recorded . Mdx mice fell down much quicker than WT mice, while mdx-ApN mice showed intermediate resistance (Fig. 5a). The grip test measures strength of forelimb or of combined fore- and hindlimb muscles . The force developed by forelimbs of mdx mice was ~36 % lower than that of WT mice, while ApN overexpression completely rescued forelimb strength (Fig. 5b). When combined fore- and hindlimb force was measured, muscular strength of mdx mice was halved when compared to WT mice, while mdx-ApN mice showed intermediate values (Fig. 5c), indicating enhanced muscle force in the presence of ApN.
Resistance to fatigue was evaluated by an eccentric exercise also designed to investigate muscle injury. On the 3rd day of the exercise, WT mice covered the maximum distance (100 m), the running distance of mdx mice fell drastically (~24 m), while that of mdx-ApN mice was not statistically different from that of WT ones (Fig. 5d and Additional file 2: Movie S2).
Effects of adiponectin on skeletal muscle injury
Creatine kinase and lactate dehydrogenase activities, two markers of muscle damage in plasma, measured herein in sedentary conditions, were ~6.7- and 5.5-fold higher in mdx than in WT mice, respectively, while both activities declined by over 40 % in mdx-ApN mice (Fig. 5e, f).
Sarcolemmal integrity was more directly evaluated by using EBD. EBD extravasation was quantified in different muscle types either in basal state (not shown) or after repeated downhill treadmill exercise (Fig. 5g). The EBD content of forelimbs was markedly increased in mdx mice (7-fold for BB and 3-fold for TB) compared to WT ones, and this content was halved in mdx-ApN mice. Likewise, the EBD content of the four hindlimb muscles tested was 2- to 6-fold higher in mdx mice than in WT ones, and this increase was partially (G, EDL) or completely (TA, S) reversed by ApN overexpression (Fig. 5g). The insets illustrate representative muscle sections under fluorescence microscopy: the proportion of damaged (fluorescent) fibers within each muscle corroborates the quantitative data shown in the histograms (Fig. 5g). Hence, ApN partially or totally restored sarcolemmal integrity and abrogated muscle injury in each type of skeletal muscles tested.
Effects of adiponectin on AMPK signaling pathway
Because ApN activates AMPK by binding to AdipoR1 in muscle, thereby triggering beneficial effects on the metabolic syndrome  and because AMPK is involved in skeletal muscle remodeling , we explored the AMPK signaling pathway.
The expression of total AMPK was similar in the three groups of mice; however, the active phosphorylated form was lower in the tibialis anterior muscle of mdx mice than in WT ones (Fig. 6a). Similarly, the expression of the deacetylase SIRT1 was markedly reduced in mdx mice compared to WT mice (Fig. 6b). Both AMPK phosphorylation and SIRT1 expression were completely or partially restored in the skeletal muscle of mdx-ApN mice (Fig. 6a, b). PGC-1α is a downstream event of this signaling cascade. Expression of total PGC-1α was not modified in any groups and the deacetylated form, which is necessary for PGC-1α activation, was not modified in mdx mice. However, mdx-ApN mice showed a sharp (~40 %) decrease in PGC-1α acetylation (Fig. 6c). Because PGC-1α is a transcriptional coactivator, it has the potential to alter the expression of numerous genes. More specifically, it can induce a myofiber shift toward a more oxidative phenotype with increased expression of utrophin A [30, 31]. Accordingly, expression of Myh7, a specific marker of slow twitch, oxidative (type I) myofibers was increased in tibialis anterior of mdx-ApN mice, while that of Myh1, a marker of fast twitch, glycolytic fibers was decreased (Fig. 6d, e). Moreover, both mRNA and protein levels of utrophin A, an autosomal analog of dystrophin , which were slightly augmented in regular mdx mice likely to compensate the lack of dystrophin , were further upregulated in mdx-ApN mice (~3–4-fold vs. WT) (Fig. 6f, g). Taken together, these data indicate a significant activation of the AMPK-SIRT1-PGC-1α axis in mdx-ApN mice.
Effects of adiponectin on NF-κB activity in mdx muscles
NF-κB is a pleiotropic transcription factor modulating immune, inflammatory, survival, and proliferative responses . To further characterize the molecular mechanisms responsible for the protective effects of ApN, we examined NF-κB activity by two different approaches.
First, we measured the nuclear translocation of NF-κB p65 subunit. Tibialis anterior sections were immunolabeled and the percentage of NF-κB marked nuclei in myofibers was counted: this percentage was 4.5-fold higher in mdx than in WT mice, but this rise was halved in mdx-ApN mice (Fig. 6h, i). Second, we quantified the active phosphorylated form of NF-κB (P-p65 on Ser536) by Western blot (Fig. 6j). P-p65 activation was ~4-fold higher in tibialis anterior of mdx mice than in WT mice, and this enhanced activation was again halved in mdx-ApN mice. Hence, the hyperactivity of NF-κB in muscles of mdx mice was attenuated by ApN. This effect persisted in old mice (Additional file 1: Figure S1D).
Effects of adiponectin on inflamed human myotubes
Finally, we tested the direct effects of ApN in primary cultures of human myotubes. Because TNFα expression was markedly elevated in muscles of mdx mice, and to mimic the inflammatory microenvironment of DMD, we challenged the myotubes with an inflammatory stimulus (TNFα/IFNγ) (Fig. 7). TNFα combined with IFNγ induced its own gene expression and that of another inflammatory cytokine, IL-6. ApN treatment abrogated these inductions (Fig. 7a, b).
Consistent with this, ApN reduced the rise of TNFα mRNAs in response to this pro-inflammatory cocktail or increased the mRNA levels of IκB (an inhibitor of NF-κB) in the presence of non-targeting (NT) siRNAs [compare the first two histograms (black vs. white column) of each panel; (Fig. 7c, d)]. These anti-inflammatory effects of ApN were abolished by siRNA silencing of genes encoding for either AdipoR1, SIRT1, or PGC-1α (Fig. 7c, d). Hence, each of these components appears to be necessary for the anti-inflammatory action of ApN (Fig. 8).
In this inflammatory setting, ApN treatment also slightly upregulated utrophin A mRNA in human myotubes with intact dystrophin (Fig. 7e).
A crucial finding of this study is that we evidenced a decrease of ApN in mdx mice. Another novel observation is that ApN correction yields striking and long-lasting attenuation of muscle inflammation and injury and improves muscle function.
We unambiguously showed that plasma ApN is decreased in mdx mice, in line with recent serum proteome data, which were however qualitative and obtained in a very limited number (n = 3) of mdx mice . Such a decrease is relevant as it may justify therapeutic correction. We further demonstrated that it may be ascribed to reduced ApN production by fat tissue, the main contributor to systemic levels. This reduced production may in turn result from the systemic inflammatory environment in DMD . TNFα indeed repressed ApN expression in adipocytes . By contrast, circulating ApN was almost normalized in mdx-ApN mice due to homotopic overexpression of ApN.
As a result, mdx-ApN mice exhibited marked reduction of muscular inflammation as shown by decreased expression of pro-inflammatory cytokines and lower infiltration by both T-lymphocytes and macrophages. As in other tissues , ApN could also promote in muscle macrophage polarization toward an anti-inflammatory phenotype as suggested by decreased expression of CD68, a M1 marker and increased expression of IL-10, which activates the anti-inflammatory and tissue-healing M2 phenotype. Markers of oxidative stress were also reduced in mdx-ApN mice. All these data are in agreement with our previous study carried out in ApN-KO mice, which exhibited a contrario higher signs of muscular inflammation and oxidative stress, which were corrected by muscular electrotransfer of the ApN gene . Herein, we further show that the presence of ApN is crucial to counterbalance inflammation and oxidative stress in skeletal muscle even when this inflammation is extremely severe and long-lasting such as in dystrophic muscle.
Besides its anti-inflammatory properties, ApN also positively affects the skeletal myogenic program. ApN has been reported to activate muscle satellite cells, which are major participants in muscle regeneration  and to induce differentiation and fusion of C2C12 myoblasts . Herein, the skeletal muscle of mdx-ApN mice displayed partial or complete restoration of MyoD and Myf5, two positive regulatory factors of the proliferative stage [27, 28] as well as of Mrf4, a regulator of the early differentiation phase . Myogenin, another marker of this early differentiation phase, was even upregulated. Taken together, these data indicate a more efficient skeletal myogenic program in mdx-ApN mice.
Both anti-inflammatory and myogenic properties may contribute to ApN protection against muscle injury. Upregulation of utrophin may also be a crucial contributor. Thus, ApN overexpression strikingly reduced both plasma CK and LDH levels and fiber membrane damage in all dystrophic muscles, as shown by in vivo staining with EBD. Accordingly, mdx-ApN mice improved global muscular force and exercise endurance in vivo. Conversely, ApN-KO mice exhibited lower peak tetanic forces in muscles stimulated in situ, while mice with muscle-specific disruption of AdipoR1 showed reduced treadmill exercise endurance [8, 38].
Although the anti-diabetic and metabolic effects of ApN are well described in skeletal muscle, the mechanisms underlying its anti-inflammatory/protective properties are only poorly studied. These molecular mechanisms were therefore investigated ex vivo and in vitro. As we did not find overt signs of apoptosis in our 8-week-old mdx mice (data not shown), we did not explore the sphingolipid ceramide pathway  but rather the AMPK axis. Phosphorylated AMPK and SIRT1 expression were reduced in skeletal muscle of mdx mice, while ApN partially or completely restored these levels. The activity of PGC-1α is enhanced by AMPK via phosphorylation and by SIRT1 via deacetylation . Here, ApN stimulated PGC-1α deacetylation in mdx mice. Stimulation of the AMPK-SIRT1-PGC-1α may protect against muscle dystrophy by activating several biological processes . First is upregulation of utrophin A together with the induction of a muscle fiber shift toward a more oxidative phenotype. Recent work has shown that pharmacological interventions (AICAR,…) that induce a more oxidative phenotype conferred morphological and functional improvements in mdx mice . However, the induction of utrophin A appears to be a prerequisite to observe these benefits, which were detectable only in mdx mice, but not in double-KO mice (mdx mice which were also deficient in utrophin). Several studies have reported that utrophin can restore sarcolemmal integrity and serve as a surrogate to dystrophin in dystrophic muscle . In this paper, utrophin appears to be a new target of ApN. Second is repression of NF-κB activity. PGC-1α has been reported to repress the phosphorylation of NF-κB family member p65, thereby inhibiting its transcriptional activity and subsequent pro-inflammatory cytokine production in C2C12 cells . SIRT1 could also suppress NF-κB signaling via deacetylation of the p65 subunit . Repressing NF-κB activity is relevant in the context of dystrophinopathy: on one hand, NF-κB signaling is persistently elevated in DMD mouse models and patients , and suppresses the myogenic program [27, 28]; on the other hand, inhibiting this pathway has been reported to exert protective effects in mouse models of muscle injury [11, 42]. We also originally found that AdipoR1 as well as SIRT1 and PGC-1α were crucial components of the anti-inflammatory action of ApN in human myotubes, a finding that seems to be verified in human dystrophic muscle cells (S. Lecompte, M. Abou-Samra, R. Boursereau, L. Noel, S.M. Brichard: Anti-inflammatory potential of Adiponectin in human dystrohic myotubes, in preparation). Third, additional biological processes not studied herein could also participate (like ApN-  and AMPK-mediated autophagic removal of dysfunctional proteins ). Taken together, our data suggest that ApN exerts its protective effects on skeletal muscle, by binding to AdipoR1 and activating the AMPK-SIRT1-PGC-1α pathway, thereby leading to NF-κB repression and utrophin upregulation (Fig. 8). Compared to other pharmacological agents targeting this signaling cascade in mdx mice (for review, see ), the improvement brought about by ApN, at physiological concentrations, is impressive and long-lasting.
The only medications so far shown to be effective in delaying the progression of DMD are glucocorticoids [43, 44]. However, adverse effects of glucocorticoids must be considered: growth retardation and weight gain, bone demineralization and fracture risk, cataracts, as well as behavioral disturbance in DMD boys. Other side effects involve glucose intolerance, hypertension, gastrointestinal problems, and Cushingoid appearance [43, 45]. Conversely, long-term treatment with ApN, which has been tested so far only in mouse, was not accompanied by major side effects. Transgenic mice overexpressing human adiponectin even showed increased longevity, which was ascribed to attenuation of oxidative DNA damage . ApN may offer several other advantages over glucocorticoids. Unlike glucocorticoids, ApN increases insulin sensitivity , does not induce muscle atrophy but rather reduces proteolysis , upregulates utrophin (our own data) and enhances the myogenic program, prevents obesity [12, 46], and protects against hypertension .
Adiponectin proves to be an extremely powerful hormone that protects muscle against inflammation, oxidative stress, and injury, even when the abnormalities are extremely severe and long-lasting such as in dystrophic muscle. This raises new therapeutic perspectives not only in myopathy but also in several other diseases, in which excessive inflammation plays a triggering or worsening pathogenic role.
adiponectin receptors 1 and 2
AMP-activated protein kinase
- ApN mice:
mice overexpressing adiponectin
- ApN-KO mice:
adiponectin knockout mice
cluster of differentiation 3
cluster of differentiation 68
Duchenne muscular dystrophy
Evans blue dye
extensor digitorium longus
- Mdx mice:
a mouse model of DMD
- Mdx-ApN mice:
Mdx mice that overexpress adiponectin
myogenic factor 5
myosin heavy chain 1, 3 (eMyHC), 6 (Mrf4), and 7
nuclear factor kappa B
peroxisome proliferator-activated receptor-γ coactivator-1α
phosphorylated p65 subunit of NF-κB
peroxisome proliferator-activated receptor alpha
peroxiredoxin 3 and 5
TATA box-binding protein
tumor necrosis factor alpha
- WT mice:
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This work was supported by grants from the Belgian Telethon, French Association against Myopathies (AFM Téléthon), the Foundation of Scientific and Medical Research (1.5097.12 and T.0212.13), and the General Division of Scientific Research (ARC 12 -17/047). We are grateful to Aurore Lafosse for providing the human muscle samples.
The authors declare that they have no competing interests.
MAS and SMB conceived and designed the study. MAS and LN performed the mouse crossing, sample extraction, and immunohistochemistry on mouse tissue; MAS and MCM analyzed and interpreted the immunohistochemistry results. MAS, OS, and PhG performed in vivo studies on mice and analyzed the results. MAS and SL performed the Western blot and immunoprecipitation on mice as well as siRNA experiments on human myotubes; MAS and SL analyzed the results. MAS and LN performed the RT-qPCR analysis and interpreted the results. MAS and SMB wrote the manuscript. MAS, PhG, SL, OS, and SMB edited the manuscript. All authors have read and given approval of the final version of the manuscript.
Sophie Lecompte and Olivier Schakman contributed equally to this work.
Effects of adiponectin on markers of oxidative stress and inflammation in muscles of 1-year-old mdx mice. A pdf file containing a supplementary figure.
Effects of adiponectin on mdx mice subjected to downhill treadmill running. A short mp4 movie showing the effect of adiponectin on mdx mice endurance.
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Abou-Samra, M., Lecompte, S., Schakman, O. et al. Involvement of adiponectin in the pathogenesis of dystrophinopathy. Skeletal Muscle 5, 25 (2015). https://doi.org/10.1186/s13395-015-0051-9