Abstract
Force loss in skeletal muscle exposed to eccentric contraction is often attributed to injury. We show that EDL muscles from dystrophin-deficient mdx mice recover 65% of lost force within 120 min of eccentric contraction and exhibit minimal force loss when the interval between contractions is increased from 3 to 30 min. A proteomic screen of mdx muscle identified an 80% reduction in the antioxidant peroxiredoxin-2, likely due to proteolytic degradation following hyperoxidation by NADPH Oxidase 2. Eccentric contraction-induced force loss in mdx muscle was exacerbated by peroxiredoxin-2 ablation, and improved by peroxiredoxin-2 overexpression or myoglobin knockout. Finally, overexpression of γcyto- or βcyto-actin protects mdx muscle from eccentric contraction-induced force loss by blocking NADPH Oxidase 2 through a mechanism dependent on cysteine 272 unique to cytoplasmic actins. Our data suggest that eccentric contraction-induced force loss may function as an adaptive circuit breaker that protects mdx muscle from injurious contractions.
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Introduction
Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused by deleterious mutations in the DMD gene, rendering non-functional forms or complete absence of the protein dystrophin1. Dystrophin is normally enriched at subsarcolemmal structures known as costameres, where it links the cortical actin cytoskeleton to the extracellular matrix through interactions with a membrane-bound glycoprotein complex2,3. DMD is one of the most common and severe forms of muscular dystrophy, affecting ~1:4000 boys4. Dystrophin deficiency leads to progressive weakness and deterioration of skeletal muscle beginning at 3 to 5 years of age. DMD patients typically become non-ambulatory by 12 years of age, with death ensuing by the second or third decade due to cardiac or respiratory failure5. Although several treatments exist, including ventilatory support and use of corticosteroids6,7, there is no cure for DMD.
Much of the mechanistic understanding of DMD has been elucidated in the dystrophin-deficient mdx mouse model, which encodes a nonsense mutation in exon 23 of the DMD gene ablating dystrophin protein expression8,9. Although the mdx mouse presents a milder phenotype compared to DMD patients10, several aspects of the disease are recapitulated in the model, including pervasive muscle weakness11, substantial histopathology due to repetitive rounds of muscle degeneration and regeneration12, and elevated serum creatine kinase levels13. Landmark studies by Sweeney and colleagues14 and Moens et al.15 demonstrated that mdx skeletal muscles are particularly sensitive to precipitous loss of contractile function after performing eccentric contractions (ECCs). With validation by many laboratories around the world as a highly robust and reproducible phenotype of murine dystrophy, the measurement of force loss induced by ECCs in mdx mice has emerged as an important quantitative readout for the efficacy of potential DMD therapies16,17. However, the molecular mechanism by which ECC force loss occurs in mdx muscle is poorly understood.
ECC force loss in mdx muscle is frequently referred to as contraction-induced “injury” or “damage”, implying that some form of slowly reversible damage has occurred within the myofiber that would take days to fully recover18. Recent studies suggest that morphological defects at the neuromuscular junction19, loss of sarcolemmal excitability20, and myofibrillar dysfunction21 all contribute to ECC force loss in mdx muscle. Several signaling mechanisms have also been implicated, including calcium22,23, Akt/PKB kinase24, neuronal nitric oxide synthase25, and redox pathways26. The effect of reactive oxygen species (ROS) on ECC force loss is particularly interesting considering recent discoveries of aberrant stretch-activated ROS in mdx skeletal muscle27,28,29,30.
In this study, we demonstrate that isolated mdx skeletal muscle recovers 65% of lost force production within 120 min of ECC and loses minimal force if the interval between eccentric contractions is increased from 3 to 30 min. To gain a mechanistic understanding of ECC force loss, we employed isobaric tags for relative and absolute quantification (iTRAQ) proteomics to identify proteins that were differentially expressed in skeletal muscle of mdx mice overexpressing nonmuscle γcyto-actin (mdx/Actg1-TG), which we have previously shown are significantly protected against ECC force loss31. We identified the antioxidant enzyme peroxiredoxin-2 (PrxII) as significantly decreased in mdx muscle compared to wild type (WT), but restored to WT levels in mdx/Actg1-TG mice. We verify that hyperactive NADPH oxidase 2 (NOX2)-dependent ROS production contributes to ECC force loss and likely causes proteolytic degradation of hyperoxidized PrxII. Ablation of PrxII exacerbated ECC force loss in mdx muscle, while overexpression of PrxII led to a dose-dependent protection against ECC force loss. We also demonstrate that myoglobin participates in ECC force loss in mdx muscle, likely through the production of hydroxyl radicals via Fenton chemistry. We further establish that oxidation-sensitive cysteine 272 unique to γcyto- and βcyto-actin is required to protect mdx muscle from ECC force loss while blocking NOX2-mediated ROS production. Finally, we show that overexpression of PrxII leads to increased sarcolemmal damage in mdx muscle exposed to eccentric contractions in vivo. Together, these data suggest that ECC may drive a transient, redox-based inhibition of contractility that protects dystrophin-deficient muscle from more catastrophic structural damage caused by subsequent high-force contractions.
Results
Rapid recovery of ECC force loss in mdx skeletal muscle
Our standard ECC protocol incorporates a 3 min interval between the 10 ECCs to eliminate fatigue, which is corroborated by the lack of force loss when isolated mdx extensor digitorum longus (EDL) muscles perform 10 more energy consumptive isometric contractions32,33 (Fig. 1a). Imposing 10 ECCs on the contralateral EDL resulted in the expected 90% drop in force; however, we observed 65% recovery of lost force production within 2 h (Fig. 1a). More surprisingly, the ECC force loss measured in mdx EDL muscles was significantly attenuated when the interval between ECC was increased from 3 to 30 min (Fig. 1b). These data demonstrate that dystrophin-deficient mdx muscle can rapidly recover from the perturbation imposed by one or multiple ECCs.
Overexpression of γcyto-actin protects mdx muscle from ECC force loss
We previously generated a mouse model that overexpresses γcyto-actin specifically in skeletal muscle (Actg1-TG) to levels that replace 40% of αskeletal-actin in myofibrils34 (Fig. 1c, d) and which significantly protects mdx muscle from ECC force loss31 (Fig. 1e). To address whether protection of mdx muscle from ECC force loss depends specifically on the γcyto-actin isoform, we crossed transgenic mice (Coco) that overexpress alpha-cardiac actin (αca-actin) specifically in skeletal muscle35 onto the mdx background (mdx/Coco). Similar to the robust expression of γcyto-actin in mdx/Actg1-TG (Fig. 1c, d), muscles from mdx/Coco animals all showed high αca-actin expression that was uniformly distributed throughout the muscle fibers (Fig. 1f, g). In contrast to mdx/Actg1-TG mice (Fig. 1e), however, EDL muscles from mdx/Coco animals were not significantly protected from ECC force loss (Fig. 1h). These data led us to conclude that some feature specific to γcyto-actin is necessary to protect mdx muscles from ECC force loss.
Overexpression of γcyto-actin restores PrxII levels in mdx muscle
To begin to understand how γcyto-actin overexpression protects mdx muscle from ECC force loss, we performed 8-plex isobaric tags for relative and absolute quantification (iTRAQ)-based mass spectrometry analysis36 on tibialis anterior (TA) muscle lysates isolated from mdx/Actg1-TG mice controlled against non-transgenic mdx littermates. The iTRAQ screen initially identified 1963 proteins representing all major protein constituents of adult myofibers in both mdx and mdx/Actg1-TG muscle (Supplementary Data 1). After applying a 1% false discovery rate to the initial protein list, 144 high-confidence proteins survived (Supplementary Data 2), with only 2 proteins demonstrating significantly different levels between mdx and mdx/Actg1-TG muscles. One differentially expressed protein was γcyto-actin, upregulated 28-fold in mdx/Actg1-TG over mdx, while the second protein PrxII was significantly upregulated 3.75-fold in mdx/Actg1-TG over mdx. In addition to confirming the iTRAQ result, western blot analysis with PrxII-specific antibodies demonstrated that PrxII is significantly decreased in mdx muscle compared to WT and restored to WT levels in mdx/Actg1-TG mice (Fig. 2a, b). In contrast, PrxII levels in mdx/Coco muscle overexpressing αca-actin were not different from mdx muscle (Fig. 2a, b). PrxII is one member in a family of six sulfhydryl-dependent cellular peroxidases that reduce endogenous hydrogen peroxide (H2O2)37. Western blot analyses for the other five family members revealed that PrxI, PrxIII, and PrxVI levels were not different between WT, mdx, and mdx/Actg1-TG muscles, while PrxIV and PrxV were substantially elevated in mdx and mdx/Actg1-TG compared to WT (Fig. 2c). Thus, PrxII was the only peroxiredoxin significantly altered in mdx muscle (decreased) and restored to its WT level in mdx/Actg1-TG (Fig. 2c).
NOX2 ablation rescues PrxII levels and attenuates ECC force loss in mdx muscle
PrxII mRNA levels were not different between WT, mdx, and mdx/Actg1-TG muscles (Supplementary Fig. 1a,b), suggesting the loss of PrxII protein in mdx muscle is post-transcriptional. Recovery of PrxII levels in mdx/Actg1-TG muscle does not seem to involve a direct interaction between PrxII and γcyto-actin, as PrxII did not bind to F- or G-actin in vitro (Supplementary Fig. 1c-f) or in vivo (Supplementary Fig. 1g). Three groups recently demonstrated increased expression of NOX2 subunits in mdx muscle, which were shown to produce significantly more ROS (ultimately in the form of H2O2) in response to mechanical stretch27,29,30. Because pharmacological inhibition of NOX2 by apocynin was also shown to protect mdx muscle from ECC force loss27, we performed experiments to elucidate the relationship between NOX2 and PrxII in mdx muscle. We confirmed that several NOX2 subunits (gp91phox, p67phox, p22phox, and Rac1) were increased in mdx muscle and show that levels remained elevated in mdx/Actg1-TG muscle (Supplementary Fig. 2a). We next compared PrxII protein levels in WT, mdx, and mdx/p47–/– muscle, which is ablated for the p47phox subunit necessary for NOX2 activity38. PrxII was restored to WT levels in mdx/p47–/– muscle (Fig. 2d), supporting a role for NOX2-dependent ROS production in the loss of PrxII from mdx muscle.
Peroxiredoxins are known to undergo irreversible hyperoxidation at conserved peroxidatic cysteine residues leading to inactivation37,39 and degradation via the 20S proteasome40. Therefore, we performed western blot analysis on WT, mdx, and mdx/p47–/– muscle lysates using antibodies specific to hyperoxidized peroxiredoxin41. The level of hyperoxidized peroxiredoxin was significantly increased in mdx muscle compared to WT, and was fully restored to WT levels in mdx/p47–/– muscle (Fig. 2e). While hyperoxidized PrxII can be reactivated by sulfiredoxin-catalyzed reduction42, we did not detect expression of sulfiredoxin in skeletal muscle (Supplementary Fig. 2b). Finally, mdx/p47–/– muscle was significantly protected from ECC force loss compared to mdx muscle (Fig. 2f). Collectively, these data suggest that aberrant NOX2-dependent ROS signaling leads to PrxII hyperoxidation and degradation in mdx muscle.
Myoglobin knockout protects mdx muscle from ECC force loss
In skinned WT rodent myofibers, H2O2 can cause significant decrements in Ca2+-activated force when myoglobin is included in the bathing medium43. The combined effect is thought to be caused by hydroxyl radicals produced by the Fenton reaction of H2O2 with Fe2+ in myoglobin44. Given that mdx ECC force loss depends on an intact muscle fiber21,24,45, we investigated whether myoglobin mediates the inhibitory effect of ROS on the contractile function of mdx muscle fibers exposed to ECC. We crossed myoglobin knockout mice46 (mb–/–) onto the mdx background to generate mdx/mb–/– mice. In verifying the absence of myoglobin in mdx/mb–/– muscle by western blot analysis (Fig. 3a), we also showed that myoglobin levels are significantly decreased in mdx muscle and partially restored in mdx/p47–/– muscle. Most importantly, knockout of myoglobin significantly protected mdx muscle from ECC force loss to the same extent as treatment of mdx muscle with the antioxidant N-acetylcysteine47 (Fig. 3b). These data suggest that myoglobin synergizes with ROS to effect ECC force loss in mdx muscle.
PrxII ablation exacerbates ECC force loss in mdx muscle
To further understand the role of PrxII in mdx ECC force loss, we crossed PrxII knockout mice48 (PrxII–/–) onto the mdx background to generate mdx/PrxII–/– mice. Western blot analysis of PrxII+/+, PrxII+/–, and PrxII–/– muscle lysates verified PrxII antibody specificity (Supplementary Fig. 3a) and confirmed the absence of PrxII in mdx/PrxII–/– muscle (Fig. 4a). Hematoxylin and eosin (H&E) staining of muscle cryosections revealed that PrxII deletion resulted in a small, but significant exacerbation of histopathology in mdx muscle without an effect on WT muscle histology (Fig. 4b, c). In our standard ECC protocol that imposes a 10% change in muscle length to maximize force loss in mdx muscle, PrxII–/– muscle was not susceptible to ECC force loss (Supplementary Fig. 3b), while ECC force loss in mdx/PrxII–/– tracked to that measured in mdx (Fig. 4d). However, mdx/PrxII–/– muscles showed significantly greater force loss than mdx muscle when exposed to a milder ECC protocol utilizing a 5% length change that elicits lower eccentric force (Fig. 4d). These data show that PrxII knockout increases the susceptibility of mdx muscle to ECC force loss.
PrxII overexpression protects mdx muscle from ECC force loss
Based on the detrimental effect of PrxII ablation on mdx muscle (Fig. 4), we tested the hypothesis that PrxII overexpression would protect mdx muscle from ECC force loss. We generated four lines of transgenic mice that overexpress PrxII specifically in skeletal muscle and crossed each line onto the mdx background to obtain four distinct lines of mdx/PrxII-TG mice. Quantitative western blot analysis demonstrated PrxII overexpression to 1×, 12×, 58× and 112× over WT levels in the four lines (Supplementary Fig. 4a,b). In our standard ECC protocol, we observed a clear dose-dependent protection of mdx muscle from ECC force loss with the greatest effect measured when PrxII was overexpressed 58× over WT (Fig. 5a, b). H&E staining of muscle cryosections from the 58× overexpressing mdx/PrxII-TG line revealed a small but significant decrease in the number of centrally nucleated fibers compared to mdx (Fig. 5c, d). Because restoration of PrxII to 1× WT levels did not protect mdx muscle from ECC force loss (Fig. 5a, b), the loss of PrxII from mdx muscle is not the primary cause of ECC force loss in mdx muscle, but rather likely a consequence of excessive ROS produced by NOX2 in response to mechanical activation.
Protection of mdx muscle from ECC force loss by γcyto-actin requires Cys272
The protection of mdx muscle from ECC force loss by overexpression of γcyto-actin, but not αca-actin (Fig. 1c–h) led us to re-examine their highly homologous primary sequences. Interestingly, γcyto-actin and βcyto-actin each contain 6 Cys residues while αsk-actin and αca-actin only contain 5 Cys residues (Supplementary Fig. 5). The additional Cys unique to γcyto-actin and βcyto-actin is located at position 272 (Supplementary Fig. 5, green highlight, blue circle) and has been shown to be the most reactive with H2O249. To investigate the role of Cys272 within γcyto-actin in protecting mdx muscle from ECC force loss, we generated transgenic mouse lines overexpressing the C272A mutant of γcyto-actin (C272A-TG) as well as βcyto-actin (Actb-TG) specifically in skeletal muscle and crossed the lines onto the mdx background to identify those that best match γcyto-actin overexpression in mdx/Actg1-TG (Fig. 6a). In addition, recombinant γcyto-actin (for mdx/C272A-TG) and platelet actin (for mdx/Actb-TG) were used to generate standard curves for quantitative western blot analysis to verify equivalent expression of each actin transgene (Supplementary Fig. 6a-c). Uniformity of C272A and βcyto-actin overexpression was verified by immunofluorescence analysis (Fig. 6b), while H&E staining revealed no obvious change in the histopathology of mdx muscle associated with overexpression of C272A or βcyto-actin (Supplementary Fig. 6d). Most interestingly, βcyto-actin overexpression protected mdx muscle from ECC force loss to the same extent as γcyto-actin, while ECC force loss in mdx/C272A-TG was not different from mdx (Fig. 6c). Finally, we measured the rate of NOX2-dependent ROS production in response to cyclic stretch of single myofibers38 isolated from WT, mdx, mdx/Actg1-TG, mdx/C272A-TG, and mdx/Actb-TG mice (Fig. 6d). Stretch-dependent, NOX2-mediated ROS signaling was significantly greater in mdx and mdx/C272A-TG compared to WT, mdx/Actg1-TG, or mdx/Actb-TG (Fig. 6d). These data demonstrate that γcyto-actin and βcyto-actin overexpression protects mdx muscle from ECC force loss by blocking the stretch-dependent NOX2-mediated production of ROS and show that Cys272 is necessary for inhibition.
Increased sarcolemmal damage in mdx muscle overexpressing PrxII following in vivo ECC
The rapid but mostly reversible inhibition of force production in mdx muscle exposed to ECC led us to consider that it may actually protect mdx muscle from damage analogous to an electrical circuit breaker. However, disabling the circuit breaker could lead to greater damage to mdx muscle exposed to ECC. To test this hypothesis, we measured sarcolemmal damage in WT, mdx, and 58X mdx/PrxII-TG following 70 eccentric contractions in vivo (Fig. 7a, b). While the unstressed contralateral muscle of mdx/PrxII-TG mice displayed similar levels of Evans blue dye (EBD) uptake compared to mdx, they presented with significantly more (27% vs. 14% in mdx) EBD-positive myofibers following 70 in vivo eccentric contractions (Fig. 7a, b). These data suggest that disabling ROS-mediated inhibition of force loss leads to greater injury following in vivo ECC in mdx muscle.
Discussion
Our data best fit a model in which PrxII functions as an off-switch to regulate stretch-activated NOX2 signaling in normal skeletal muscle50, but is lost from mdx muscle through hyperoxidation and proteolytic degradation effected by aberrant NOX2-mediated ROS production. PrxII is known to suppress redox-mediated growth factor signaling51,52,53, while NOX2 in mdx skeletal muscle has been demonstrated to produce significantly more ROS38, particularly in response to mechanical stretch as occurs during ECC27,29,30,54. Importantly, treatment with the NOX2 inhibitor apocynin27, the non-specific antioxidant N-acetylcysteine47, or catalase overexpression55 has been shown to protect mdx muscle from ECC force loss, mirroring the effect we observed in mdx/Actg1-TG (Fig. 1e), mdx/p47–/– (Fig. 2f), mdx/mb–/– (Fig. 3b), mdx/PrxII-TG (Fig. 5a), and mdx/Actb-TG EDL muscles (Fig. 6c) (for more physiological parameters of all mouse lines, see Supplementary Table 1).
Our stretch-activated ROS experiments with single myofibers from transgenic models overexpressing γcyto-actin, βcyto-actin, or the C272A mutant of γcyto-actin (Fig. 6d) suggest that cytoplasmic actin overexpression directly inhibits NOX2 activity in mdx skeletal muscle. In vitro binding experiments and studies in nonmuscle cells have shown that actin can inhibit NOX2 activity by directly binding and sequestering the p40phox, p47phox, and/or p67phox regulatory subunits56,57. Alternatively, the additional redox-sensitive Cys272 unique to γcyto- and βcyto-actins49,58 may serve to shunt ROS-mediated oxidation away from conserved sulfhydryls necessary for contractile function. Future experiments will address both possibilities.
One poorly understood feature of ECC force loss in mdx muscle is its dependence on intact myofibers, because skinned fibers from mdx mice are no more susceptible to ECC than WT21,24,45. In studies of muscle fatigue, ROS in the form of H2O2 is thought to exert inhibitory effects on contractile proteins, yet extremely high concentrations of H2O2 are required to cause significant decrements in Ca2+-activated force loss in skinned myofibers44,59. However, the concentration of H2O2 required to elicit force loss is greatly reduced when myoglobin is included in the bathing medium43,44, which results in the production of highly reactive hydroxyl radicals through the reaction of H2O2 with Fe2+ in myoglobin44. Our experiments in mdx/mb–/– mice (Fig. 3) suggest that myoglobin and H2O2 may catalyze similar Fenton chemistry in mdx muscle to cause ECC force loss with concomitant oxidative degradation of myoglobin.
While the ROS-based perturbations tested here by us and reported by others previously27,47,55,60 all demonstrated significant protection of mdx muscle from ECC force loss, the measured protection is incomplete. Other studies have implicated elevated cytosolic calcium61,62,63,64, loss of neuromuscular junction or sarcolemmal membrane excitability19,20, neuronal nitric oxide synthase25, and Akt/PKB signaling24 in mdx ECC force loss and our results are neither incompatible with nor mutually exclusive of such mechanisms. For example, NOX2 negatively regulates Akt activation in skeletal muscle exposed to oxidative stress65, while the activity of ion channels important for membrane excitability are sensitive to oxidation66. Although stretch-activated calcium channels are clearly one downstream effector of the ROS produced by NOX228, it is not clear how an increase in cytosolic calcium could affect rapidly reversible ECC force loss as reported here (Fig. 1a, b) and elsewhere67,68. Perhaps the rapidly reversible component of ECC force loss, measured here over the course of 2 h, is due to reversible oxidation of one or more proteins regulating muscle contraction, while the slowly reversible component, or force loss that is recovered in the timeframe of several days69, is due to calcium-activated proteolysis of other muscle regulatory proteins. Alternatively, both the rapidly reversible and slowly reversible components of ECC force loss in mdx muscle could result from oxidative stress. In some pathological states, peroxiredoxins (including PrxII) are subject to over-oxidation such that reversibly sulfenylated cysteine residues become irreversibly sulfinylated or sulfonylated53,70. Such hyperoxidation may occur in proteins involved with contractility in mdx muscle, leading to their irreversible inactivation and contributing to the slowly reversible component of ECC force loss.
As noted in the Introduction, ECC force loss in mdx muscle is often referred to as “contraction-induced injury,” or “contraction-induced damage,” and muscle damage is operationally defined “as weakness which recovers very slowly after activity with a time course (4–8 days) similar to repair or regeneration”18. We measured rapid recovery of force in isolated mdx EDL muscles exposed to ECC (Fig. 1a). While our rapid recovery data are supported by other studies67,68, they are incompatible with the above definition of muscle damage. On the other hand, the rapidly reversible component of ECC force loss fits well with a reversible ROS-mediated inhibition of contractile force. This immediate and reversible inhibition of force in mdx may benefit the muscle in the long run, since more injurious contractions performed in vivo on mdx mice with decreased ROS signaling (mdx/PrxII-TG) led to increased sarcolemmal permeability (Fig. 7). Rather than serving as a readout for muscle damage, ours and others’ data collectively lead us to propose that ECC force loss may instead function as an adaptive circuit breaker that protects dystrophin-deficient muscle from potentially cell-lethal structural damage caused by continually repeated high force contractions.
Methods
Mice
All animals were housed and treated in accordance with the standards set by the University of Minnesota Institutional Animal Care and Use Committee. All animal experiments were approved by the University of Minnesota Institutional Animal Care and Use Committee under protocol numbers 1207A17501, 1506-32699A, and 1806-36018A. Mice were maintained on regular diet in a specific-pathogen-free facility on a 12 h light/dark cycle with continuous access to food and water. All wild-type mice used in this study were on the C57BL/10SnJ background. All transgenic overexpression mice are skeletal muscle-specific using the human skeletal actin (HSA) promoter. All mice on the mdx background utilized the C57BL/10ScSn-Dmdmdx/J strain of mdx mice from The Jackson Laboratory. Transgenic mice overexpressing γcyto-actin on the mdx background (mdx/Actg1-TG) have been previously described31. Transgenic mice overexpressing αcardiac-actin (Coco) have been previously described35 and bred onto the mdx background in this study. Mice with a genetic deletion of the NOX2 scaffolding subunit p47phox (p47–/–) were obtained from The Jackson Laboratory (B6(Cg)-Ncf1m1J/J) and bred onto the mdx background as previously described38. Mice with a genetic knockout of myoglobin (mb–/–) have been previously described46 and were bred onto the mdx background in this study. Mice lacking peroxiredoxin-2 (PrxII–/–) have been previously described48 and were rederived from sperm donated by Dr. Dae-Yeul Yu (Korean Research Institute of Bioscience and Biotechnology) and bred onto the mdx background in this study. Transgenic mice overexpressing peroxiredoxin-2 (PrxII-TG), γcytoC272A (C272A-TG), and βcyto-actin (Actb-TG) are described in this paper (Methods – Cloning and generation of transgenic mice), and all three were bred onto the mdx background, resulting in mdx/PrxII-TG, mdx/C272A-TG, and mdx/Actb-TG mice. For all transgenic lines on the mdx background, non-transgenic mdx littermates were used as controls. Animals used for physiological experiments were all 3 months of age, while mice used for all other experiments were 3–6 months of age. All mice used in this study were male.
Antibodies and reagents
Primary antibodies used for western blotting were: mouse monoclonal anti-γcyto-actin71 (1:1000; clone 2–4), mouse monoclonal anti-αcardiac-actin (1:1000; Sigma, A9357), rabbit polyclonal anti-PrxII (1:1,000; Sigma, R8656), mouse monoclonal anti-Dystrophin (1:100; Leica, NCL-DYS1), mouse monoclonal anti-Utrophin (1:100; Santa Cruz, sc-33700), mouse monoclonal anti-GAPDH (1:10,000; Sigma, G8795), rabbit polyclonal anti-GAPDH (1:10,000; Sigma, G9545), rabbit polyclonal anti-PrxI (1:500; Abcam, ab15571), mouse monoclonal anti-PrxIII (1:500; Abcam, ab16751), mouse monoclonal anti-PrxIV (1:500; Abcam, ab16943), mouse monoclonal anti-PrxV (1:500; Abcam, ab16944), rabbit polyclonal anti-PrxVI (1:1000; Sigma, P0058), rabbit polyclonal anti-PrxSO3 (1:200; Abcam, ab16830), rabbit polyclonal anti-Myoglobin (1:5000; Dako, A0324), mouse monoclonal anti-βcyto-actin (1:1000; Sigma, A1978), mouse monoclonal anti-gp91phox (1:1000; BD Biosciences, 611414), mouse monoclonal anti-p67phox (1:1000; BD Biosciences, 610912), rabbit polyclonal anti-p22phox (1:200; Santa Cruz, sc-20781), mouse monoclonal anti-Rac1 (1:2000; Cytoskeleton, ARC03), rabbit polyclonal anti-p47phox (1:1000; EMD Millipore, 07-500), rabbit polyclonal anti-p40phox (1:500; EMD Millipore, 07-501), and rabbit polyclonal anti-Sulfiredoxin (1:1000; Proteintech, 14273-1-AP). Secondary antibodies used for western blotting were: DyLight 680 Goat anti-Mouse IgG (CST, 5470S), DyLight 680 Goat anti-Rabbit IgG (CST, 5366S), DyLight 800 Goat anti-Mouse IgG (CST, 5257S), and DyLight 800 Goat anti-Rabbit IgG (CST, 5151S) all at 1:10,000 dilutions.
Primary antibodies used for immunofluorescence were: rabbit polyclonal anti-γcyto-actin71 (1:500; clone 7577), mouse monoclonal anti-αcardiac-actin (1:250; Sigma, A9357), rabbit polyclonal anti-Laminin (1:1000; Sigma, L9393), rat monoclonal anti-Laminin (1:1000; Sigma, L0663), mouse monoclonal anti-βcyto-actin-FITC (1:500; Abcam, ab6277), and rabbit polyclonal anti-Dystrophin72 (1:20; clone Rb2). Secondary antibodies used for immunofluorescence were: Alexa Fluor 488 Donkey anti-Mouse IgG (ThermoFisher, A-21202), Alexa Fluor 488 Donkey anti-Rabbit IgG (ThermoFisher, A-21206), Alexa Fluor 488 Goat anti-Rat IgG (ThermoFisher, A-11006), Alexa Fluor 568 Donkey anti-Mouse IgG (ThermoFisher, A-10037), Alexa Fluor 568 Goat anti-Rabbit IgG (ThermoFisher, A-11011), and Alexa Fluor 568 Goat anti-Rat IgG (ThermoFisher, A-11077) all at 1:500 dilutions.
Other reagents used were DH5α competent cells (Invitrogen, 18258012), DH10Bac competent cells (Invitrogen, 10361012), Sf9 insect cells (ATCC, CRL-1711), N-acetylcysteine (Sigma, A7250), DCFH-DA (6-Carboxy-2′,7′-Dichlorodihydrofluorescien Diacetate) (Invitrogen, C-400), gp91ds-tat (NOX2-specific peptide inhibitor) (Bio-Synthesis Inc., Lewisville, TX), FLAG peptide (University of Minnesota Genomics Center, Minneapolis, MN), anti-FLAG M2 affinity gel (Sigma, A2220), and human platelet actin protein (Cytoskeleton, APHL99).
Ex vivo EDL force measurements
Contractile functions of EDL muscles were assessed according to methods described previously73. Mice were anesthetized with sodium pentobarbital (75–100 mg/kg body mass). EDL muscles were dissected and mounted on a 300B-LR dual-mode muscle lever system (Aurora Scientific Inc.) with 5–0 suture in a 1.2 mL bath assembly with oxygenated (95:5% O2/CO2) Krebs-Ringer bicarbonate (Krebs) buffer maintained at 25 °C. The stimulator and muscle lever system was controlled by computer using a KPCI-3108 interface board (Keithley Instruments) and TestPoint software (SuperLogics). Muscles were adjusted to their anatomical optimal length (Lo) based on resting tension, with length being measured from the distal myotendonous junction to the proximal myotendonous junction using digital calipers. Prior to performing eccentric contractions, maximal isometric tetanic force (Po) was measured every 2 min by stimulating the muscle to contract for 200 ms at 175 Hz until force plateaued, with this value being designated “pre Po”, or simply “Pre”. In our standard ECC protocol, a series of 10 eccentric contractions were performed and the peak force of each contraction was recorded. For each ECC force measurement, the muscle was passively shortened to 95% Lo and then stimulated for 200 ms while the muscle was simultaneously lengthened to 105% Lo at a velocity of 0.5 Lo/s. Each eccentric contraction was separated by 3 min of rest before performing the next eccentric contraction to prevent fatigue74. The force measured at each eccentric contraction was expressed as a percentage of the force produced during the first (“initial”) contraction. The value of “n” for all ECC experiments is defined as “number of mice”, and only one EDL per mouse was used for each experiment. This standard ECC protocol was used in Fig. 1e, h, Fig. 2f, Fig. 3b, Fig. 4d (10%: mdx and 10%: mdx/PrxII–/–), Fig. 5a, Fig. 6c, and Supplementary Fig. 3b. Experiments where variations of the standard ECC protocol were used are explained below.
For Fig. 1a, mdx muscles were subjected to either the standard ECC protocol described above or the same protocol substituting isometric contractions for eccentric contractions performed on the contralateral EDL. After each 10-contraction protocol, Po was measured immediately (Post 0’) as well as at the 20, 40, 60, 90, and 120 min timepoints (Post 20’, Post 40’, etc.). Each Po was then expressed as a percentage of the Po measured before the 10 eccentric or isometric contractions (Pre). For the eccentric protocol, statistical significance was determined for the Po measured at Post 20’ through Post 120’ compared to the Po measured at Post 0’ (see Statistical analysis).
In Fig. 1b, mdx EDLs were subjected to only 5 eccentric contractions. The first muscle used a standard 3 min of rest between each eccentric contraction, while the contralateral muscle was allowed 30 min of rest between contractions.
Figure 3b involves a group where N-acetylcysteine (NAC) treatment was performed on mdx EDLs. For this group, NAC (Sigma-Aldrich) was dissolved directly into Krebs Buffer at 20 mM immediately prior to bath assembly47. The control mdx group used standard Krebs Buffer without NAC. For both groups, EDL muscles were incubated for 30 min so NAC could efficiently penetrate the muscle before being subjected to the standard ECC protocol.
For Fig. 4d, the standard ECC protocol was used for 10%: mdx and 10%: mdx/PrxII–/– experiments (solid lines). For the other two experiments (dash lines), the standard ECC protocol was used except that a 5% length change was performed instead of a 10% change. Here, EDL muscles were passively shortened to 97.5% Lo and then stimulated for 200 ms while the muscle was simultaneously lengthened to 102.5% Lo at 0.25 Lo/s, resulting in lower peak eccentric force being generated compared to the 10% length change.
Immunoblot analysis
Gastrocnemius muscles from mice of the indicated genotypes were dissected, flash frozen in liquid N2, pulverized to a powder with a liquid N2-cooled mortar and pestle, and resuspended in 1% sodium dodecyl sulfate (SDS) in phosphate-buffered saline (PBS) with protease inhibitors (100 nM aprotinin, 1 mM benzamidine, 10 µM E-64, 10 µM leupeptin, 1 mM pepstatin A, 1 mM phenylmethanesulfonylfluoride, 1 µM calpain inhibitor I, and 1 µM calpeptin). Samples were then incubated at room temperature (RT) with end-over-end rotation for 30 min, followed by centrifugation at 20,817 × g for 10 min to clear lysates of insoluble material. Total protein concentration of the lysates was determined by A280 measurement (NanoDrop 1000, ThermoFisher Scientific). Lysates were then diluted to equal concentrations before Laemmli sample buffer was added and boiled for 5 min. Equal amounts of protein were then separated by SDS–polyacrylamide gel electrophoresis (SDS-PAGE), transferred to polyvinylidene difluoride (PVDF) membranes, blocked with 5% milk in PBS, and incubated with the indicated primary antibodies overnight at 4 °C. The next day, membranes were washed 4 × 5 min in 0.1% Tween in PBS before incubation with DyLight secondary antibodies (1:10,000 each) for 1 h at RT. Membranes were again washed 4 x 5 min before being imaged with an Odyssey Infrared Scanner (LI-COR Biosciences). Protein bands were then quantified using LI-COR Image Studio software.
Muscle histology and immunofluorescence
TA muscles from each mouse line were cryopreserved in melting isopentane for 30 s and 10 µm transverse cryosections were obtained (Leica CM3050 S). For histology, sections were stained with H&E and imaged on a Leica DM5500 B microscope equipped with a Leica HC PLAN APO 20× objective. Centrally nucleated fibers (CNFs) were counted using the Cell Counter plugin on ImageJ software (NIH) and expressed as a percentage of the total number of myofibers (%CNFs). For immunofluorescence, sections were fixed in 4% paraformaldehyde in PBS at RT for 10 min and subsequently washed three times in PBS before being permeabilized in 0.1% Triton X-100 in PBS for 10 min at RT. Sections were then blocked in 5% bovine serum albumin (BSA) and 0.1% Triton X-100 in PBS for 1 h at RT before incubating with primary antibodies overnight at 4 °C. Slides were then washed three times in PBS before incubating with Alexa Fluor secondary antibodies (1:500 each) for 1 h at RT. Sections were finally wash three times in PBS and mounted in ProLong Gold Antifade with 4′,6-diamidino-2-phenylindole (DAPI) to visualize nuclei (ThermoFisher Scientific). Images were acquired on a Deltavision PersonalDV deconvolution microscope equipped with an Olympus UApo 20x objective.
iTRAQ proteomics
TA muscles were dissected from 5 mdx/Actg1-TG mice and 3 non-transgenic mdx littermates and pulverized into powder with a liquid nitrogen-cooled mortar and pestle. We closely followed the protein extraction and preparation steps as well as offline peptide fractionation described previously75 with slight modifications. We added 10 µL of lysis buffer per milligram of tissue for protein extraction and sonicated. A 105 µL aliquot of each lysate was run in the Barocycler NEP2320 (Pressure Biosciences, South Easton, MA) after which a Bradford assay was performed to determine protein concentrations. We digested 100 µg of each sample with trypsin, performed solid-phase extraction (SPE) clean-up, and reacted 40 µg of each of the eight protein samples with one of the iTRAQ® 8-plex reagents (Sciex, Framingham, MA). iTRAQ labels 113, 114, and 115 were used to label peptides from the 3 mdx samples, while iTRAQ labels 116, 117, 118, 119, and 121 were used to label peptides from the 5 mdx/Actg1-TG samples. We mixed equal aliquots of each protein sample (40 µg), processed by SPE clean-up, and performed peptide fractionation by liquid chromatography (LC). We performed the second dimension capillary LC separation of peptides in-line with an Orbitrap Velos mass spectrometer (MS) as previously described76. Slight variations in the mass spectrometer acquisition method were: lock mass was not used, HCD activation time was 20 msec, dynamic exclusion duration was 15 s, and the minimum signal threshold for data dependent trigger was 20,000 counts.
We converted the raw MS datafiles to MGF files with MS Convert from ProteoWizard Toolkit77. We used ProteinPilot™ v4.5 (Sciex, Framingham, MA) for the database search and quantification report with the following parameters: National Center for Biotechnology Information (NCBI) RefSeq mouse (Taxonomy ID: 10088) protein database combined with the contaminants database (http://www.thegpm.org/cRAP/index.html); 8-plex peptide label sample type; cysteine methyl methanethiosulfonate; trypsin; instrument Orbi MS (1–3ppm) Orbi MS/MS; biological modifications ID focus; thorough search effort; detected protein threshold 0.05 (10%); competitive error margin 2.00; and false discovery rate (FDR) analysis invoked (with reversed database). FDR calculations were performed in ProteinPilot™ with the concatenated forward and reversed protein sequence databases according to the method previously reported78. ProteinPilot™ calculates an average protein relative fold change between two conditions along with a 95% confidence interval for the fold change and a P value for a test of the null hypothesis unity (1:1 ratio), which helps assess the statistical significance of a fold change.
It should be noted that we originally attempted to perform iTRAQ proteomics on 4 mdx/Actg1-TG mice versus 4 non-transgenic mdx littermates. After obtaining the high-confidence protein list results, we discovered that the sample labeled with iTRAQ 116, initially thought to be an mdx mouse, displayed significantly higher levels of γcyto-actin, consistent with iTRAQ labels 117, 118, 119, and 121 (mdx/Actg1-TG mice). We then re-genotyped the set of mice used in the iTRAQ proteomic screen, which revealed that the mouse labeled with iTRAQ 116 was indeed mdx/Actg1-TG, and that this mouse had been mis-genotyped or mis-labeled, resulting in 5 mdx/Acg1-TG mice and 3 non-transgenic mdx littermates instead of 4 of each genotype. Uncovering this mistake increased our confidence in the iTRAQ experiment, as the data from the screen itself unveiled the error.
Quantitative reverse transcription-polymerase chain reaction (qRT-PCR)
Gastrocnemius of WT, mdx, and mdx/Actg1-TG mice were flash frozen in liquid N2 and pulverized to a powder with a cooled mortar and pestle. Total RNA was then extracted from each sample using the Aurum Total RNA Mini Kit (Bio-Rad) following the manual’s instructions. RNA concentration and purity (A260/280 ratio) were determined using a NanoDrop 1000 spectrophotometer (ThermoFisher Scientific). Reverse transcription was performed using the iScript Advanced complementary DNA (cDNA) Synthesis Kit for qRT-PCR (Bio-Rad) using the same initial RNA amount (1 µg) for all samples. qPCR reactions were prepared with the SsoAdvanced Universal SYBR Green Supermix (Bio-Rad) and quantified on a CFX96 Real Time System C1000 Touch Thermal Cycler (Bio-Rad). Primer sets for both PrxII and HPRT (loading control) were generated with Primer-BLAST software (NIH) to amplify across an exon junction and are listed in Supplementary Table 2. Significance of gene expression differences was determined by one-way analysis of variance (ANOVA) with Tukey's post hoc test analysis. Resulting qRT-PCR reactions were further run on a 1% agarose gel for visualization.
Protein expression and purification
FLAG-tagged PrxII and Fascin-1 proteins were expressed and purified in Sf9 insect cells using the Bac-to-Bac protocol (Invitrogen). Briefly, recombinant baculoviral DNA was transfected into a small culture of Sf9 insect cells using CellFectin II (Invitrogen). After 4 days, the media containing the recombinant baculovirus were harvested and the transfected cells were analyzed for protein expression by anti-FLAG western blot. Once expression was validated, large (250 mL) cultures were incubated for 3 days with amplified baculovirus before being harvested for protein purification. For purification, cells were lysed using 1% Triton X-100 in PBS (8 mM NaH2PO4, 42 mM Na2HPO4, 150 mM NaCl, pH 7.5) containing protease inhibitors (100 nM aprotinin, 1 mM benzamidine, 10 µM E-64, 10 µM leupeptin, 1 mM pepstatin A, and 1 mM phenylmethanesulfonylfluoride) and protein was purified using ANTI-FLAG M2 affinity gel (Sigma-Aldrich) as previously described79,80,81. Proteins were dialyzed into PBS overnight at 4 °C before being concentrated and used in in vitro F-actin and G-actin binding assays (Supplementary Fig. 1c-f). Recombinant γcyto-actin was expressed in the Bac-to-Bac insect cell expression system and purified as previously described82,83 before being used as a standard curve in determination of C272A-TG and Actb-TG transgene concentrations (Supplementary Fig. 6a,b).
F-actin cosedimentation assay
A previously described F-actin high speed cosedimentation assay82 was used to measure binding properties of PrxII and Fascin-1 (positive control). Briefly, human platelet actin (Cytoskeleton) was resuspended in G-Buffer (5 mM Tris-HCl pH 8.0, 0.2 mM CaCl2, 0.2 mM ATP, and 0.5 mM DTT), then induced to polymerize with the addition of 10× Polymerization Buffer (100 mM Tris pH 7.5, 500 mM KCl, 20 mM MgCl2, and 10 mM ATP). Recombinant FLAG-PrxII or FLAG-Fascin-1 (1 µM each) was then incubated with various concentrations of F-actin (0–15 µM) for 30 min at RT. Samples then underwent high speed centrifugation at 100,000 × g for 30 min at 4 °C. Resulting supernatant and pellet fractions were subjected to SDS-PAGE, stained with Coomassie blue, and scanned using the Licor Odyssey system allowing quantification of supernatant and pellet fractions. The values from these experiments were plotted in GraphPad Prism software and nonlinear regression analysis was performed.
G-actin binding assay
Human platelet actin (Cytoskeleton) was resuspended in G-Buffer (5 mM Tris-HCl pH 8.0, 0.2 mM CaCl2, 0.2 mM ATP, and 0.5 mM DTT) to maintain actin in its globular form (G-actin). Then, 400 µL mixtures of 1 µM G-actin alone (negative control) and 1 µM G-actin + 1 µM FLAG-PrxII (experiment) were made. Then, 100 µL of both mixtures were taken as the “Load” fraction. Then, 100 µL of each protein mixture was added to 25 µL of ANTI-FLAG M2 affinity beads and incubated for 1 h at 4 °C with end-over-end rotation. The beads were then centrifuged at 106 × g for 3 min at 4 °C and the supernatant was collected as the “Void” fraction. The beads were then washed three times with 400 µL G-buffer before adding 100 µL of 0.1 mg/mL FLAG peptide in G-Buffer and incubating at RT for 10 min. Samples were then centrifuged as before and the supernatants were collected as the “Elute” fraction. To ensure the G-actin was indeed in its globular form, 100 µM of both protein mixtures was incubated at RT for 30 min before being subjected to high-speed centrifugation (100,000 x g) for 30 min at 4 °C. The supernatant and pellet fractions were then collected and run with each Load, Void, and Elute fraction on SDS-PAGE. Gels were then Coomassie stained and scanned on the Licor Odyssey imaging system.
PrxII immunoprecipitation
PrxII was immunoprecipitated from mdx/Actg1-TG muscle using the Pierce Crosslink Magnetic IP/Co-IP Kit (ThermoFisher Scientific) following the manual’s instructions. Briefly, gastrocnemius muscles from mdx/Actg1-TG mice were flash frozen and pulverized to a powder with a cooled mortar and pestle. mdx/Actg1-TG muscles were used because γcyto-actin is expressed at such low levels in WT mice that it cannot be detected with typical western blotting. Samples were then solubilized with the kit’s IP Lysis Buffer (25 mM Tris pH 7.4, 150 mM NaCl, 1 mM EDTA, 1% NP-40, and 5% glycerol) supplemented with protease inhibitors (100 nM aprotinin, 1 mM benzamidine, 10 µM E-64, 10 µM leupeptin, 1 mM pepstatin A, 1 mM phenylmethanesulfonylfluoride, 1 µM calpain inhibitor I, and 1 µM calpeptin) by incubating for 30 min at 4 °C with end-over-end rotation. Lysates were then cleared by centrifugation at 20,817 × g for 10 min at 4 °C and protein concentrations were determined using the Pierce BCA Protein Assay Kit (ThermoFisher Scientific). Samples were diluted to 0.5 mg/mL in 1 mL of IP Lysis Buffer. During the protein sample preparation, 10 µg PrxII antibody (Sigma) was coupled to Protein A/G magnetic beads and crosslinked using DSS (disuccinimidyl suberate). Diluted protein was then incubated with the crosslinked magnetic beads for 1 h at RT. Beads were washed thoroughly before the sample was eluted with low pH Elution Buffer. Load, Void, Wash, and Elute fractions collected during the immunoprecipitation were subjected to SDS-PAGE, transferred to PVDF membranes, blocked with 5% milk in PBS, and probed with PrxII (Sigma) and γcyto-actin (clone 2–4) primary antibodies overnight at 4 °C. Membranes were incubated with DyLight secondary antibodies before being scanned on the Licor Odyssey imaging system.
Cloning and generation of transgenic mice
Human peroxiredoxin-2 plasmid cDNA was purchased from DNASU Plasmid Repository (Cat #HsCD00076134), PCR amplified, inserted into the Gateway entry vector pENTR/D-TOPO (Invitrogen), and sequence verified. All PCRs were performed using PfuUltra Fusion HS DNA Polymerase (Agilent Technologies). To make recombinant FLAG-PrxII protein, pENTR/D-TOPO-PRDX2 was N-terminally FLAG-tagged (pENTR/D-TOPO-N-FLAG-PRDX2) via PCR using primers that amplified the entire plasmid with FLAG sequence overhangs. The linear PCR product was circularized via the addition of T4 polynucleotide kinase and T4 DNA ligase (New England Biolabs) and sequence verified. Once verified, the entry vector was recombined into the Gateway insect cell destination vector pDEST8 (pDEST8-N-FLAG-PRDX2) using LR Clonase II (Invitrogen) and subsequently expressed in Sf9 insect cells using the Bac-to-Bac system (Invitrogen; see Protein expression and purification). To generate the PrxII-TG transgene, pENTR/D-TOPO-PRDX2 was recombined into a pDEST8 destination vector already containing the HSA promoter followed by the VP1 intron and tandem SV40 polyadenylation sequences (pDEST8-HSA-VP1-SV40-SV40). The PrxII cDNA was inserted in-frame between the VP1 intron and the first SV40 polyadenylation sequence (pDEST8-HSA-VP1-PRDX2-SV40-SV40). The construct was transformed into DH5α bacteria cells and extracted using the Wizard Plus SV Minipreps DNA Purification System (Promega). The DNA fragment from the HSA promoter through the polyadenylation sequence was restriction digested to linearize the transgene, gel purified via the QIAEX II Gel Extraction Kit (Qiagen), and sent to the Murine Genetics Core at The Scripps Research Institute for pronuclear microinjection into fertilized C57BL/6 zygotes, which were then implanted into pseudo-pregnant female mice.
We obtained Fascin-1 cDNA (FSCN1) as a kind gift from Dr. Steven Almo of the Albert Einstein College of Medicine. FSCN1 was PCR amplified, inserted into the Gateway entry vector pENTR/D-TOPO (Invitrogen), and sequence verified. To make recombinant FLAG-Fascin-1 protein, pENTR/D-TOPO-FSCN1 was N-terminally FLAG-tagged (pENTR/D-TOPO-N-FLAG-FSCN1) via PCR using primers that amplified the entire plasmid with FLAG sequence overhangs. The linear PCR product was circularized via the addition of T4 polynucleotide kinase and T4 DNA ligase (New England Biolabs) and sequence verified. Once verified, the entry vector was recombined into the Gateway insect cell destination vector pDEST8 (pDEST8-N-FLAG-FSCN1) using LR Clonase II (Invitrogen) and subsequently expressed in Sf9 insect cells using the Bac-to-Bac system (Invitrogen; see Methods - Protein expression and purification).
To generate C272A-TG and Actb-TG transgenes, both the pDEST8-HSA-VP1-C272A-SV40-SV40 (C272A-TG) and pDEST8-HSA-VP1-ACTB-SV40-SV40 (Actb-TG) constructs were cloned based on the original pDEST8-HSA-VP1-ACTG1-SV40-SV40 (Actg1-TG) construct previously described34. The C272A-TG construct was generated via site-directed mutagenesis using the QuikChange II XL kit (Agilent Technologies, Cat. no. 200521) according to the manufacture protocols and sequence verified. Primers were designed to allow a two-nucleotide change within the codon normally encoding Cysteine to then encode for Alanine at position 272 (TGT to GCT). For Actb-TG, only the ACTG1 nucleotides that coded for the 4 γcyto-actin-specific amino acids (Glu2, Glu3, Glu4, and Ile10) were altered to instead code for the 4 βcyto-actin-specific amino acids (Asp2, Asp3, Asp4, and Val10) by editing the wobble base in each codon within the construct. This ensures any differences described between transgenic mice are only due to the altered amino acids, and not plasmid differences. The Actb-TG construct was generated via PCR using primers designed such that they amplified the Actg1-TG plasmid with ACTB-specific overhangs. The linear PCR product was circularized via the addition of T4 polynucleotide kinase and T4 DNA ligase (New England Biolabs) and sequence verified. Both constructs were transformed into DH5α bacteria cells and extracted using the Wizard Plus SV Minipreps DNA Purification System (Promega). The DNA fragment from the HSA promoter through the polyadenylation sequence was restriction digested to linearize the transgene, gel purified via the QIAEX II Gel Extraction Kit (Qiagen), and sent to the Murine Genetics Core at The Scripps Research Institute for pronuclear microinjection into fertilized C57BL/6 zygotes, which were then implanted into pseudo-pregnant female mice.
Resultant PrxII-TG, C272A-TG, and Actb-TG transgenic founder mice were identified by PCR using HSA-specific primers (Supplementary Table 2) and crossed with C57BL/10 mice to check for transgene transmission. Transgenic PrxII (PrxII-TG), γcyto-actin (C272A-TG), and βcyto-actin (Actb-TG) protein expression was assessed in several different muscles from each transgenic line crossed onto the mdx (C57BL/10ScSn-Dmdmdx/J) background using quantitative western blotting. All mdx-transgenic mice used in this study were compared with non-transgenic littermate mdx mice as controls.
Stretch-induced ROS measurements
Flexor digitorum brevus (FDB) muscles were surgically isolated and incubated in Dulbecco's modified Eagle's medium (DMEM; ThermoFisher Scientific) containing 0.1% penicillin–streptomycin (ThermoFisher Scientific) and 0.4% Collagenase A (Sigma-Aldrich) at 37 °C for 2 h. Single FDB fibers were isolated by gentle trituration in DMEM containing 0.1% penicillin–streptomycin and 10% fetal bovine serum (ThermoFisher Scientific) and incubated at 37 °C, 5% CO2 until used, typically 16–20 h later. Isolated FDB fibers were washed three times with HEPES solution (120 mM NaCl, 4.7 mM KCl, 1.8 mM CaCl2, 600 µM MgSO4, 1.6 mM NaHCO3, 130 µM NaH2PO4, 7.8 mM Glucose, and 20 mM HEPES) and loaded with 15 µM DCFH-DA (Invitrogen) for 25 min at RT in the dark. The fibers were then washed three times with HEPES solution containing either dimethyl sulfoxide (DMSO; 0.1%) or gp91ds-tat (10 µM) and the DCFH-DA dye was allowed to de-esterify for 15 min at RT in the dark. The ends of each fiber were attached to a micro-glass pipet coated with a biological adhesive (ECM Gel from Engelbreth-Holm-Swarm murine sarcoma, Sigma-Aldrich) and connected to micro-manipulators (Sutter Instruments). DCF Fluorescence (Ex: 480 nm, Em: 535/40 nm) and sarcomere length were acquired using an IonOptix system (Westwood, MA) atop a Motic AE31 microscope equipped with a 40× objective (Olympus UAP040X3/340). Each fiber was cyclically stretched to 110% of resting sarcomeric length (2–2.2 µm) at 10 µm/s for 15 min. The rate of DCF fluorescence was reported during the last 2.5 min of stretch.
Evans blue dye assay
EBD was diluted in PBS to a final concentration of 5 mg/mL and was filter-sterilized with a 0.2 µm filter. EBD was administered by intraperitoneal injection (100 µL of diluted EBD per 10 g body weight) 24 h before the mice were subjected to eccentric contractions performed in vivo as previously described84. Briefly, the left hind limb was depilated and aseptically prepared and the foot was placed in a foot plate attached to a servomotor (Model 300B‐LR; Aurora Scientific, Aurora, Ontario, Canada) and Pt–Ir electrode wires (Model E2‐12; Grass Technologies, West Warwick, RI, USA) were inserted percutaneously on either side of the peroneal nerve. Contractions were induced via stimulation of the peroneal nerve at a frequency of 150 Hz by a stimulator and stimulus isolation unit (Models S48 and SIU5, respectively; Grass Technologies). Anterior crural muscles were injured by performing 70 electrically stimulated eccentric contractions (each contraction separated by 10 s), during which the foot was passively rotated from 0° to 19° dorsiflexion followed by 38° of plantarflexion at 2000°/s using the optimized voltage. Both the TA subjected to ECC and the contralateral TA (control) of each mouse were dissected and cryopreserved in melting isopentane before obtaining 10 µm cryosections at the mid-belly of each muscle. Sections were fixed in −20 °C acetone for 5 min, washed in PBS, blocked for 30 min at room temperature with 5% BSA/PBS, and counterstained with laminin (1:500; Sigma-Aldrich L9393) for 2 h at RT. Sections were then washed in PBS and incubated with anti-Rabbit Alexa Flour 488 (1:500; ThermoFisher Scientific) for 1 h at RT. Sections were washed a final time in PBS and mounted in ProLong Golf Antifade with DAPI (ThermoFisher Scientific). Images were acquired on a Leica DM5500 B microscope equipped with a Leica HC PLAN APO 10× objective and stitched together with LASX software (Leica) to allow visualization of the entire TA. MyoVision software (https://www.uky.edu/chs/muscle/myovision) was used to determine the percentage of EBD-positive myofibers in whole-TA images85.
Statistical analysis
All statistics were calculated using GraphPad Prism software. All data are presented as mean ± SEM in force loss graphs, dot plots, and bar graphs. In force loss graphs, two-way ANOVA with Bonferroni post hoc test analyses were performed. For dot plots and bar graphs, one-way ANOVA with Tukey's post hoc test analyses were performed. For applicable experiments, the exact value of n (defined by number of animals) and the definition of significance can be found in the figure legend.
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD009680. A reporting summary for this article is available as a Supplementary Information file.
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Acknowledgements
The iTRAQ proteomic screen was performed at the University of Minnesota Center for Mass Spectrometry and Proteomics, with LeeAnn Higgins and Todd Markowski providing much appreciated assistance in sample preparation and data analysis. The mdx/Coco transgenic mice were kindly provided by Dr. Kay Davies of the Medical Research Council, along with Dr. Nigel Laing and Dr. Kristen Nowak of the University of Western Australia. Rederivation of the PrxII–/– mouse line was performed at the University of Minnesota Mouse Genetics Laboratory. Pronuclear injection and embryo implantation of transgenic mice were accomplished at The Scripps Research Institute Murine Genetics Core. Fascin-1 cDNA was a kind gift from Dr. Steven Almo of the Albert Einstein College of Medicine. We also thank Nigel Laing of the University of Western Australia for helpful comments on the manuscript. This study was supported by National Institute of Arthritis and Musculoskeletal and Skin Diseases grants to J.M.E. (R01AR049899) and G.G.R. (R01AR061370). J.T.O., J.J.B., and K.A.B. were supported by the National Institutes of Health Training Program in Muscle Research (T32AR007612). J.T.O. was further supported by the National Institute of Aging Training Program for Functional Proteomics of Aging (T32AG029796). J.J.B. was also supported by a University of Minnesota Doctoral Dissertation Fellowship.
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J.T.O. designed and performed experiments, analyzed data, and wrote the paper; A.L., K.A.B. and D.A.L. designed and performed skeletal muscle physiology experiments; R.A.-Z. performed single myofiber stretch-induced ROS experiments; X.P. and J.J.B. performed molecular cloning for the generation of transgenic mice; B.J.P. contributed conceptually to the paper; D.Y.-Y., D.J.G., and G.G.R. provided reagents and mice; J.M.E. designed experiments, wrote the paper, and supervised the project.
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Olthoff, J.T., Lindsay, A., Abo-Zahrah, R. et al. Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle. Nat Commun 9, 5104 (2018). https://doi.org/10.1038/s41467-018-07639-3
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DOI: https://doi.org/10.1038/s41467-018-07639-3