Abstract
Pseudotrophic muscular dystrophy is a common clinical skeletal muscle necrotic disease, among which Duchenne muscular dystrophy (DMD) is the predominant. For such diseases, there is no clinically effective treatment, which is only symptomatic or palliative treatment. Oxidative stress and chronic inflammation are common pathological features of DMD. In recent years, it has been found that the pathophysiological changes of skeletal muscle in DMD mice are related to muscle stem cell failure. In the present study, we established a DMD mice model and provided tocotrienol (γ-tocotrienol, GT3), an antioxidant compound, to explore the relationship between the physiological state of muscle stem cells and oxidative stress. The results showed that the application of GT3 can reduce ROS production and cellular proliferation in the muscle stem cells of DMD mice, which is beneficial to promote the recovery of muscle stem cell function in DMD mice. GT3 treatment improved the differentiation ability of muscle stem cells in DMD mice with increasing numbers of MyoD+ cells. GT3 application significantly decreased percentages of CD45+ cells and PDGFRα+ fibro-adipogenic progenitors in the tibialis anterior of DMD mice, indicating that the increased inflammation and fibro-adipogenic progenitors were attenuated in GT3-treated DMD mice. These data suggest that increased ROS production causes dysfunctional muscle stem cell in DMD mice, which might provide a new avenue to treat DMD patients in the clinic.
Introduction
DMD is a recessive neuromuscular disease linked to the X chromosome. The birth rate of affected men is about 1/3,600–6,000. The disease is mainly caused by frameshift deletion, meaningless or repeated mutations of the gene encoding dystrophin (dystrophin) on the X chromosome (Xp21.2) (; ). Dystrophin is an important part of a protein complex, which connects the muscle cytoskeleton and extracellular matrix to maintain the integrity and stability of the muscle membrane (). Dystrophin binds to F-actin through its cytoplasmic N-terminal domain. The extracellular C-terminal domain of dystrophin binds to β-dystrophic glycan, which acts as a bridge and anchor protein. The mutation of dystrophin leads to the disruption of dystrophin-related glycoprotein complexes, which causes membrane instability and sensitizes to various stresses and muscle fiber necrosis. DMD is a progressive disease (). Its pathological characteristics are progressive muscle damage and weight loss. The patient developed symptoms of muscle weakness when they are young. The motor function will gradually decline when they are growing up. The patients will gradually unable to walk independently and die of heart or respiratory failure around the age of 20 (). The existing treatment approaches of DMD, such as steroid therapy, stem cell transplantation and gene therapy, have certain defects and limitations (; ; ).
Chronic inflammation and oxidative stress are common pathophysiological characteristics of DMD (). Excessive ROS will negatively affect cell proliferation, resulting in cell death because of high levels of oxidative stress, damaging lipids, protein and DNA (; ). Some research results indirectly support the existence of high levels of ROS in DMD muscle stem cells. The abnormal vascular distribution of DMD muscle leads to ischemia and hypoxia (). Therefore, increased ROS production may be one of the reasons for DMD muscle cell dysfunction. Recent studies have shown that pathophysiological changes of skeletal muscle in DMD mice models are related to muscle stem cells exhaustion. Muscle stem cells can be detected between the basement membrane and the muscle fiber membrane, which is in a quiescent status under steady state condition. They are the main source of regulating the growth and regeneration of new skeletal muscle and essential for the stability and regeneration of skeletal muscle throughout the life cycle (). Cellular reactive oxygen species is a double product of oxidative phosphorylation, which can regulate physiological activities of stem cells (). On the other hand, there is evidence that the main effect of antioxidants on the muscles of DMD mice model is to inhibit cell death and promote muscle cell maturation by reducing oxidative stress ().
Vitamin E is a widely used natural supplement with strong antioxidant, neuroprotective and anti-inflammatory properties (), which can regulate the peroxidation reaction and control the production of free radicals in the body. There are eight different subtypes of these compounds, which are collectively referred to as tocols (; ). It has always been believed that α-tocopherol subtype is the main subtype of vitamin E’s antioxidant and anti-inflammatory effects. There is conclusive evidence that γ-tocotrienol (GT3) is the advanced subtype of vitamin E, which has stronger antioxidant properties than the former (; ). It was shown that stem cells can efficiently keep in an undifferentiated status after supplementation of antioxidants, which benefits to prevent stem cell exhaustion (). However, whether GT3 can enhance the function of muscle stem cells in DMD mice is still unknown. In this study, mdx mice were generated as a pathological model of DMD. GT3 treatment was used to evaluate whether GT3 can ameliorate the phenotypic and functional defects of muscle stem cells in the DMD mice model.
Materials and Methods
Animals
For this study, we used 40-week-old DMD knockout mice with a genetic background of C57BL/6J and ordinary C57BL/6J strain SPF male mice, weighing 26–28 g, from the Institute of Model Animals of Nanjing University. The animals were maintained on a regular 12-h day and night changes with free access to food and water during the whole experimental period. The environmental temperature was controlled at 23 ± 3°C and the relative humidity was maintained between 30 and 70%. The whole animal experiment process is strictly in accordance with the 3R principle of experimental animals to give the experimental animals humane care. Mice were divided randomly into four groups: wild type (WT), DMD knockout mice (DMD) and the two types of mice which were treated with GT3. The animal welfare and Ethics Committee of Nanchang University reviewed and approved the disposal method of the animals during the experiment (NCU-CLA-2019-319).
γ-tocotrienol Treatment
γ-tocotrienol was purchased from Cayman Inc. (Item No: 10008494). γ-tocotrienol was maintained in the absolute ethanol with a concentration of 10 mg/ml. After drying with nitrogen, γ-tocotrienol powder was dissolved in the pre-prepared solvent to make the final concentration 4 mg/ml. The solvent is composed of anhydrous ethanol, Tween 80, polyethylene glycol 400, and ultrapure water with a ratio of 2:1:1:16. Mice were subcutaneously injected with GT3 (50 mg/kg). The same volume of solvent injection was used as controls. All mice were sacrificed at 48 h after treatment. Bilateral tibialis anterior were collected, weighed, and processed for further study.
Histology and Immunostaining
Tibialis anterior were fixed in 4% PFA. Paraffin-embedded sections (5 µm) were collected. Hematoxylin and Eosin (HE) staining was performed according to a conventional staining procedure. The mean girth of muscle bundle in cross section was calculated.
The expression of Pax7 and proliferating cell nuclear antigen (PCNA) was assessed in muscle cells by immunohistochemistry staining. Citrate solution (pH = 6.0) is used for antigen retrieval and endogenous peroxidase was eliminated with 3% hydrogen peroxide. Sections were then washed three times in 1 × PBS, which was then followed by an overnight incubation at 4°C with mouse monoclonal primary antibody (Pax7, 1:100, Abcam ab55494; PCNA, 1:400, Boster Biological Technology co. ltd. BM0104; MyoD1,1:400, Affinity AF7733; PDGFRα, 1:200, Bioss bs-0231R). Slides were incubated with goat anti-mouse secondary antibody for 30 min at RT and followed by three washes in 1 × PBS. The color is developed by diaminobenzidine method. Pictures were taken under microscope (Olympus). Numbers of Pax7, PCNA MyoD1, PDGFRα positive cells were counted in the cross-section area.
Quantitative Real-Time PCR
Total RNA was extracted from ipsilateral DMD and tibialis anterior of WT mice using Trizol reagent (Trans, Cat# ET111-01). A total of 1 μg of RNA was used for RT using the Reverse Transcription System (Cat#K1322; Thermoscientific) according to the manufacturer’s protocol. RT-PCR was conducted in triplicate determinants of PerfectStart Green qPCR SuperMix (Cat#AQ601; Trans) with the appropriate forward and reverse primers. For quantitative analysis of gene expression, results were averaged from three replicates in three independent experiments. Primers used for quantitative RT-PCR analysis are listed in Table 1. HPRT was used as an internal reference.
TABLE 1
| Primer sequences |
|---|
| Cyclin D1 F: 5′-ATGTTCGTGGCCTCTAAGATGAAG-3′ |
| R: 5′-CAGAAGCAGTTCCATTTGCAGCAG-3′ |
| Cyclin D2 F: 5′-CCAGGAGCTGCTGGAGTGGGAACTG-3′ |
| R: 5′-GCTTGCGGATCAGGGACAGCTTCTC-3′ |
| P27 F: 5′-GGTCTCAGGCAAACTCTGAGGAC-3′ |
| R: 5′-GCGAAGAAGAATCTTCTGCAG-3′ |
| HPRT F: 5′-AGCAGTACAGCCCCAAAATGGTTA-3′ |
| R: 5′-TCAAGGGCATATCCAACAACAAAC-3′ |
Primer sequences for RT-PCR.
Measurement of Muscle Stem Cells by Flow Cytometry
The muscle tissue is grinded and digested in DMEM culture medium containing 10% FBS containing 1×collagenase/dispase enzyme (1 mg/ml; Roche) for 1 h at 37°C. The supernatant is filtered to lyse the red blood cells to obtain a single cell suspension. Cells were stained with PE anti-mice/rat CD29 Antibody, PerCP/Cyanine5.5 anti-mice CD184 (CXCR4) Antibody, APC anti-mouse CD45 Antibody, APC anti-mouse CD11b Antibody. DAPI was used to exclude dead cells. All flow antibodies were ordered form Biolegend Inc. Stained cells were analyzed by flow cytometry (BD FACSVerse). CD45−CD11b−CD29+CXCR4+ cells were used to define muscle stem cells. Percentages of CD45−CD11b−CD29+CXCR4+ cells in DAPI− cells were demonstrated.
ROS Production
Cells were stained with muscle stem cell antibodies. 20 μmol/L DCFDA (Invitrogen), a probe for intracellular ROS levels, was used to stain cells for 30 min at 37°C under dark conditions. Dead cells were eliminated by DAPI. Stained cells were analyzed using a flow cytometer (BD FACSVerse). Mean fluorescence intensity (MFI) of DCFDA in muscle stem cells was calculated using a FlowJo software.
Statistics
All statistical analyses were performed using GraphPad Prism 8. Data were presented as mean ± SEM. Differences between groups are assessed using Student’s t-test and one-way or two-way analysis of variance (ANOVA), using Tukey’s multiple comparison test. Data were considered significant differences from the mean in control when p < 0.05.
Results
Loss of Dystrophin Results in Increased Myocyte Proliferation and Hypertrophy of Skeletal Muscle
Under the macroscopic view, DMD mice have significant hypertrophy of lower limb muscles (Figure 1A). We separated the tibialis anterior muscle of WT and DMD mice and weighed them for comparison, the weight of the tibialis anterior (TA) muscle of the left side showed that the muscle weight of DMD mice is significantly higher than that of WT mice (Figure 1B). There is no significant difference in body weight between WT and DMD mice. The circumference of muscle bundles was measured after HE staining. Feret’s Diameter analysis was used to calculate the average diameter of muscle fibers. The results show that the circumference of muscle bundles in DMD mice was significantly increased when compared to control mice. The former had larger mean muscle fiber diameters than the later (Figure 1C).
FIGURE 1
We then measured the proliferation status of muscle cells in tibialis anterior through PCNA immunostaining. As shown in Figure 2A, most of normal muscle cells were in a static state with almost no PCNA positive staining. However, there is a significant increase in PCNA positive staining in DMD mice, which is located between muscle cells and muscle bundles. Statistical analysis of the numbers of these PCNA positive cells suggests that the numbers of positive cells in DMD mice significantly increased when compared to muscles in WT mice. Then, we detected proliferation-related gene expression and found that there was no significant difference in the expression of Cyclin D1 and Cyclin D2 between WT and DMD mice. However, the expression of P27 was significantly decreased in DMD mice when compared to that in WT mice. These data showed that cells from tibialis anterior have increased proliferation in DMD mice compared to that in WT mice (Figure 2B).
FIGURE 2
Decreased Numbers of Satellite Cells and Increased Oxygen Free Radical Levels in DMD Mice
In addition to detecting the changes in muscle cells, the numbers of muscle stem cells were also examined in DMD mice. PAX7 was used as a characteristic marker to specific label muscle stem cells. The results showed that the numbers of muscle stem cells in DMD mice were significantly reduced (Figure 3A). Since many factors might be involved in the reduction of muscle stem cells. The increase of oxidative stress is a common factor. Therefore, the separated tibialis anterior bundles were digested into single muscle cells by collagenase. We labeled CD11b−CD45−CD29+CXCR4+ cells and separated them by flow cytometry. PAX7 immunofluorescence staining of the sorted cells showed that the sorted cells were stained with PAX7 antibody. We then compared the proportion of labeled cells in tibialis anterior cells of WT and DMD mice, demonstrating that the proportion of muscle stem cells in DMD mice was significantly lower than that in WT mice (Figure 3B).
FIGURE 3
The DCFDA probe was used to detect the levels of oxygen free radicals in muscle stem cells. As shown in Figure 4, the fluorescence intensity of DCFDA in DMD muscle stem cells significantly increased when compared to that in WT muscle stem cells. These data indicate that elevated levels of oxygen free radicals might be an important factor leading to the damage of muscle stem cells in DMD mice.
FIGURE 4
GT3 Treatment Increased the Circumference of Tibialis Anterior and Inhibited Cell Proliferation in DMD Mice
It is well known that GT3 has a strong ability to inhibit ROS production. In order to explore the role of GT3 in the injuried muscle of DMD mice, WT and DMD mice were treated with GT3 for 48 h and the tibialis anterior muscle was collected for analysis. GT3 treatment did not affect body weight in WT and DMD mice. However, the weight of the left tibialis anterior in the DMD group after GT3 treatment was significantly reduced compared that in the DMD group after vehicle treatment (Figure 5A). The circumference of muscle bundle was measured, showing that the circumference of the muscle bundle of the TA in DMD mice was increased when compared to the control group after GT3 treatment (Figures 5B,C). In addition, the Feret’s Diameter analysis was also used to compare the mean diameters of tibialis anterior fiber (Figure 5D). After GT3 treatment, the tibialis anterior fibers of DMD mice had larger mean diameters when compared to that of WT mice. Meanwhile, PCNA immunostaining was performed on the muscle. The numbers of PCNA positive cells were counted in each field (Figure 6A). The results showed that the numbers of PCNA positive cells in DMD mice after GT3 treatment were lower than that of the untreated control group, indicating that GT3 treatment can inhibit excessive cell proliferation. Similarly, we compared the gene expression of tibialis anterior cells after GT3 treatment. Our data showed that there was no statistical difference in the expression of Cyclin D1 and Cyclin D2 in tibialis anterior cells after GT3 treatment in WT and DMD mice while the expression of P27 was significantly increased in DMD muscle after GT3 treatment when compared to that in the control group (Figure 6B).
FIGURE 5
FIGURE 6
GT3 Treatment Increased Numbers of Muscle Stem Cells in the Tibialis Anterior of DMD Mice
PAX7 was used to marker muscle stem cells in the tibialis anterior muscle. As shown in Figure 7A, the numbers of muscle stem cells in DMD mice after GT3 treatment were significantly increased compared with the numbers of untreated control group. After GT3 treatment, the percentages of muscle stem cells in DMD mice were increased, which is consistent with the data from PCNA immunostaining. Collectively, these findings suggest GT3 can increase the numbers of muscle stem cells in DMD mice. In addition, we also demonstrated the same results by labeling muscle stem cells with flow cytometry, showing that GT3 treatment significantly increased percentages of muscle stem cells (Figure7B).
FIGURE 7
GT3 Treatment can Improve the Differentiation of Muscle Stem Cells in DMD Mice
In order to verify the effect of GT3 treatment on the function of muscle stem cells in DMD mice, MyoD1 antibody was used to detect their differentiation ability. As shown in Figure 8, the numbers of MyoD1 positive staining in DMD mouse muscle cells were significantly decreased when compared to that in WT mice. However, it was found that there was a significant increase in the numbers of MyoD1 positive cells in the GT3 treatment group of DMD mice when compared to that in the vehicle group. These results suggest that GT3 treatment can improve the differentiation ability of muscle stem cells in DMD mice.
FIGURE 8
GT3 Reduces Inflammation and Fibrosis in the Tibialis Anterior of DMD Mice
One of the pathological manifestations of DMD is inflammatory infiltration. CD45 was used as a specific marker of inflammatory response. CD45+ cells were analyzed by flow cytometry to measure inflammation levels in the tibialis anterior. As shown in Figure 9, percentages of CD45+ cells in DMD mice were significantly increased when compared to those in WT mice. In comparison to the vehicle-treated DMD mice, the percentages of CD45+ cells in GT3-treated mice were significantly decreased. These data indicate that GT3 can reduce inflammatory infiltration of tibialis anterior in DMD mice.
FIGURE 9
Additionally, increased fibrosis is also a major pathological feature of DMD mice. PDGFRα+ cells in skeletal muscle mesenchymal progenitor named fibro-adipogenic progenitors can differentiate into fibroblasts and adipocytes which are thought to play an important role in the fibrosis process (). The data from PDGFRα staining showed that DMD mice had more fibro-adipogenic progenitors in the tibialis anterior when compared to that in WT mice, which was attenuated after GT3 treatment (Figure 10). Taken together, these data display that GT3 treatment inhibits inflammatory infiltration and fibro-adipogenic progenitors in the tibialis anterior caused by loss of dystrophin, which may alleviate the fibrotic symptoms of DMD.
FIGURE 10
GT3 Treatment Reduced the Production of Oxidative Free Radicals in Muscle Stem Cells in DMD Mice
We previously demonstrated that muscle stem cells in DMD mice have increased levels of oxygen free radicals. Whether GT3 treatment can decrease oxygen free radicals in DMD mice was then investigated. We used the probe DCFDA to compare the changes of oxidative free radical levels in DMD muscle stem cells before and after GT3 treatment. The results showed that GT3 treatment significantly reduced the levels of oxidized free radicals in muscle stem cells in DMD mice when compared to those in control mice (Figure 11).
FIGURE 11
Discussion
The impaired muscle regeneration accompanying the exhaustion of the satellite cell pool is a major feature of DMD. Muscle damage in patients with DMD is manifested by extremely low regenerative capacity, fibrosis, fat deposition, inflammatory infiltration, and fiber atrophy (). At present, there is no effective long-term treatment for DMD. The commonly used clinical method is corticosteroid therapy, but the effect is not satisfactory (). Muscle stem cells are good potential repair factors for damaged muscles due to their omnipotence. Therefore, investigators are exploring the effects of stem cell therapy on DMD. In addition, there are some data showing that DMD progression results in part from a cell-autonomous failure of muscle stem cells to maintain the damage-repair cycle initiated by dystrophin deficiency. It has been shown that maintaining the function of muscle stem cells has therapeutic significance for DMD (). The responses of muscle stem cells to injury or disease are an activation process. They then re-enter the cell cycle and proliferate to produce a pool of progenitor cells marked by the expression of the myogenic transcription factor MyoD1. The damaged muscle can be replenished and repaired through proliferation and differentiation of muscle stem cells (). We specifically labeled the muscle stem cells in DMD knockout mice and found that numbers of muscle stem cells were significantly reduced. On the contrary, the numbers of proliferating cells were significantly increased when compared to that in normal mice. Previous studies have shown that muscle fibers in DMD mice with less than 52 weeks of age are compensated by vigorous regeneration (), which may partly explain the increase in muscle fibers caused by the depletion of muscle stem cells in DMD mice.
In addition, the researchers isolated muscle fibers for cell culture and found that the asymmetric division rate of satellite cells in DMD mice was significantly lower than that in WT mice. These data, suggest that the proportion of cells capable of dividing with self-renewal potential was significantly lower in DMD mice (). Similarly, through isolating muscle stem cells for primary culture to detect their self-renewal and differentiation ability by fluorescence, it was found that muscle stem cells in DMD mice were highly active, leading to excessive consumption. Muscle stem cells in DMD mice have features with high levels of aging cells and ROS production. These abnormalities in DMD mice can be partially ameliorated by administration of nutritional drugs (). Our present data show that loss of dystrophin results in the increased proliferation of muscle stem cells, which is supported by increasing PCNA+ cells and decreasing P27 expression in the tibial anterior of DMD mice. GT3 application in vivo can reduce numbers of PCNA+ cells and increase P27 expression in DMD mice. The effects and mechanisms of GT3 on the proliferation of muscle stem cells from DMD mice will be further investigated in cell culture condition in our future study.
At present, stem cell therapies have achieved the goal of regenerating damaged tissue by supplementing specific stem cell populations. For patients with DMD, the main therapeutic objective is to reconstruct the muscle stem cell pool containing the myostatin receptors, so as to restore the presence of myostatin expressing muscle fibers and recover muscle function (). However, the treatment was not successful in moving from mice to human. Only small amounts of myodystrophy were detected after the transplants (). This may be due to immune rejection, limited numbers and migration of injected cells, and a large numbers of cell death after transplantation. These studies demonstrates that there was still a long way to go in trying to improve the development of DMD by allogeneic or autologous stem cell transplantation therapy. Patients with DMD urgently need a new treatment that can directly act on stem cells to repair or alleviate their damage.
The continuous contraction of muscle fibers will cause a significant increase in the production of active oxygen free radicals (). These molecules regulate a variety of redox-sensitive signaling pathways and play key roles in cellular processes such as gene expression and protein modification. ROS can modify the proteins on the mitochondrial membrane, leading to osmotic swelling. Excessive ROS can lead to oxidative damage to lipids, protein and DNA, leading to cell death or abnormal cell growth. Oxidative stress and mitochondrial dysfunction play a vital role in the pathophysiological process of muscular dystrophy (; ). Membrane fragility caused by muscular dystrophy leads to intracellular Ca2+ imbalance, which in turn leads to mitochondrial dysfunction and interleukin-6 (IL-6)-mediated ROS release. The increase in ROS levels in turn induces mitochondrial DNA (mtDNA) damage, resulting in production of large amounts of active oxygen. This vicious circle exacerbates muscle fiber damage and cell death (). When excessive ROS is produced, it leads to oxidative stress. Reactive oxygen species produced by skeletal muscle contraction will affect muscle adaptation and function. Our analysis of oxidative free radicals in muscle stem cells of WT and DMD mice found that there was a significant increase in ROS production in muscle stem cells of DMD mice. The presence of excessive ROS will lead to a series of pathophysiological changes. ROS overproduction plays an important role in muscle stem cells in the functional damage of DMD mice. Inhibiting ROS production may be an effective measure to improve the function of muscle stem cells in DMD mice.
Phenolic compounds have powerful antioxidant activity, which helps to regulate the peroxidation reaction in the body and controls the production of free radicals. These compounds also help to protect cells from oxidative damage caused by free radicals, which could be generated by risk factors such as radiation exposure (). Both tocopherols and tocotrienols have been shown to be relatively non-toxic, even at higher doses. It has been shown that tocopherols provide significant survival advantages (). Compared with tocopherols, tocotrienols can penetrate cell membranes, removing chain-spreading oxygen free radicals, and capturing singlet oxygen and other active substances (; ).
In the present study, tocotrienol (GT3) is applied to evaluate whether it could reduce excessive oxidative free radicals in muscle stem cells of DMD mice. GT3 can selectively inhibit the PI3K/Akt pathway, Ras/Raf/Erk signal transduction, HMG-CoA reductase and transcription factor NF-κB, and participate in the regulation of various physiological activities of the body (). Transcriptomics analyses showed that GT3 regulates the expression of genes related to inflammation, protein transport and cellular redox (; ). It has the functions of inducing cell apoptosis, inhibiting colony formation, inhibiting cell survival and cell proliferation (). In the present study, we found that the levels of oxidative free radicals in muscle stem cells of DMD mice were significantly reduced after application of GT3.This may help to reduce the excessive loss of muscle stem cells during muscle regeneration and thus increase the numbers of muscle stem cells. On the other hand, data from previous studies are consistent with our conclusion that GT3 can improve the differentiation ability of muscle stem cells to repair muscle exhaustion in DMD mice (; ). Therefore, out data suggest that application of GT3 can reduce the ROS production of muscle stem cells and improve their physiological activities in a harmless way. It is worth noting that numbers of CD45+ cells were increased in muscle cells of DMD mice, which represents an inflammatory infiltration of muscle cells. This inflammatory response can be partially ameliorated by other drug application (; ). This is similar to our findings showing that GT3 treatment significantly decreased percentages of CD45+ cells in DMD mice, indicating that GT3 ameliorates inflammatory infiltration. In addition, overactivation of the PDGFRα pathway in DMD mice has previously been shown to lead directly to fibrosis and impede muscle repair (). These mesenchymal progenitors, expressing PDGFRα in the skeletal muscle, were shown to express pro-fibrotic genes in response to TGF-β (). These data implicate that PDGFRα+ fibro-adipogenic progenitors play an important role in the fibrogenic process (). Further data displayed that PDGFRα+ cells were appeared in the DMD connective tissue thickening region, which partly explains the significance of PDGFRα for muscle fibrosis (; ). Studies have found that drug treatment can limit the differentiation of mesenchymal progenitors, thereby reducing the transition to PDGFRα+ fibro-adipogenic progenitors, controlling fibrosis progression (). Consistently, the use of GT3 in the present study may partially inhibit the increase of fibro-adipogenic progenitors caused by excessive activation of this pathway to control further development of fibrosis. These data from our study indicatethat GT3 treatment can alleviate the pathological symptoms of DMD.
Our study proves for the first time that the application of GT3 can reduce ROS production of muscle stem cells in DMD mice, which may be beneficial to promote the recovery of muscle stem cell function and muscle morphology in DMD mice. However, it is unknown whether GT3 treatment has long-term effects on muscle stem cells in DMD mice, which will be further investigated in near future. The exact reason why DMD mice did not reproduce the human DMD phenotype is unclear. Some researchers believe that the phenotype in DMD gene knockout mice might be compensated through muscular nutrition by up-regulating a protein similar in structure to dystrophin, which is utrophin (). To overcome this barrier in DMD mice, a new type of double-knockout mouse was created, which knocked out both dystrophin and utrophin genes, making its symptom phenotype more severe and thus clinically close to the phenotype of patients with DMD. In addition, DBA/2J-congenic DMD mdx mice (D2-mdx) have been found to have earlier onset and more pronounced dystrophy phenotype which is closer to clinicopathological characterization (; ). Therefore, D2-mdx is increasingly used in the research of DMD instead of original model of C57/BL phenotype.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
The animal study was reviewed and approved by Nanchang University.
Author contributions
SY, BK, and LS designed and performed research, analyzed data and wrote the paper; SY, JY, HZ, and RD performed research; HF, JZ, ZY, and HZ analyzed data; LS designed research, analyzed data and wrote the paper.
Funding
The study was partially supported by the National Natural Science Foundation of China (Grant No. 81760328, 82073484, 81860026); Jiangxi Provincial Natural Science Foundation (20192BBG70043, 20202ACB206009); Interdisciplinary Innovation Fund of Natural Science in Nanchang University (9166-27060003-YB13). We thank the College of medicine of Nanchang University for providing comprehensive experimental services. We thank the animal facility of the Nanchang University for maintaining mice colony.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcell.2022.820520/full#supplementary-material
References
1
AhsanH.AhadA.IqbalJ.SiddiquiW. A. (2014). Pharmacological Potential of Tocotrienols: A Review. Nutr. Metab. (Lond)11 (1), 52. 10.1186/1743-7075-11-52
2
AokiY.MiyatakeS.Shimizu-MotohashiY.TakedaS. i. (2016). Anti-inflammatory Drugs for Duchenne Muscular Dystrophy: Focus on Skeletal Muscle-Releasing Factors. Dddt10, 2745–2758. 10.2147/DDDT.S110163
3
BellaP.FariniA.BanfiS.ParoliniD.TonnaN.MeregalliM.et al (2020). Blockade of IGF2R Improves Muscle Regeneration and Ameliorates Duchenne Muscular Dystrophy. EMBO Mol. Med.12 (1), e11019. 10.15252/emmm.201911019
4
BischoffR. (1986). A Satellite Cell Mitogen from Crushed Adult Muscle. Developmental Biol.115 (1), 140–147. 10.1016/0012-1606(86)90235-6
5
ChamberlainJ. R.ChamberlainJ. S. (2017). Progress toward Gene Therapy for Duchenne Muscular Dystrophy. Mol. Ther.25 (5), 1125–1131. 10.1016/j.ymthe.2017.02.019
6
ChenC.-C.LiuT.-Y.HuangS.-P.HoC.-T.HuangT.-C. (2015). Differentiation and Apoptosis Induction by Lovastatin and γ-tocotrienol in HL-60 Cells via Ras/ERK/NF-κB and Ras/Akt/NF-Κb Signaling Dependent Down-Regulation of Glyoxalase 1 and HMG-CoA Reductase. Cell Signal.27 (11), 2182–2190. 10.1016/j.cellsig.2015.07.014
7
ColeyW. D.BogdanikL.VilaM. C.YuQ.Van Der MeulenJ. H.RayavarapuS.et al (2016). Effect of Genetic Background on the Dystrophic Phenotype Inmdxmice. Hum. Mol. Genet.25 (1), 130–145. 10.1093/hmg/ddv460
8
ContrerasO.RebolledoD. L.OyarzúnJ. E.OlguínH. C.BrandanE. (2016). Connective Tissue Cells Expressing Fibro/adipogenic Progenitor Markers Increase under Chronic Damage: Relevance in Fibroblast-Myofibroblast Differentiation and Skeletal Muscle Fibrosis. Cell Tissue Res364 (3), 647–660. 10.1007/s00441-015-2343-0
9
ContrerasO.SolimanH.TheretM.RossiF. M. V.BrandanE. (2020). TGF-β-driven Downregulation of the Wnt/β-Catenin Transcription Factor TCF7L2/TCF4 in PDGFRα+ Fibroblasts. J. Cel Sci133 (12), jcs242297. 10.1242/jcs.242297
10
FoxH.MillingtonL.MahabeerI.van RuitenH. (2020). Duchenne Muscular Dystrophy. BMJ368, l7012. 10.1136/bmj.l7012
11
FrankD. E.SchnellF. J.AkanaC.El-HusayniS. H.DesjardinsC. A.MorganJ.et al (2020). Increased Dystrophin Production with Golodirsen in Patients with Duchenne Muscular Dystrophy. Neurology94 (21), e2270–e2282. 10.1212/WNL.0000000000009233
12
GordonB. S.Delgado DíazD. C.KostekM. C. (2013). Resveratrol Decreases Inflammation and Increases Utrophin Gene Expression in the Mdx Mouse Model of Duchenne Muscular Dystrophy. Clin. Nutr.32 (1), 104–111. 10.1016/j.clnu.2012.06.003
13
HammersD. W.HartC. C.MathenyM. K.WrightL. A.ArmelliniM.BartonE. R.et al (2020). The D2.Mdx Mouse as a Preclinical Model of the Skeletal Muscle Pathology Associated with Duchenne Muscular Dystrophy. Sci. Rep.10 (1), 14070. 10.1038/s41598-020-70987-y
14
IeronimakisN.HaysA. L.JanebodinK.MahoneyW. M.Jr.DuffieldJ. S.MajeskyM. W.et al (2013). Coronary Adventitial Cells Are Linked to Perivascular Cardiac Fibrosis via TGFβ1 Signaling in the Mdx Mouse Model of Duchenne Muscular Dystrophy. J. Mol. Cell Cardiol.63, 122–134. 10.1016/j.yjmcc.2013.07.014
15
IeronimakisN.HaysA.PrasadA.JanebodinK.DuffieldJ. S.ReyesM. (2016). PDGFRα Signalling Promotes Fibrogenic Responses in Collagen‐producing Cells in Duchenne Muscular Dystrophy. J. Pathol.240 (4), 410–424. 10.1002/path.4801
16
JoeA. W. B.YiL.NatarajanA.Le GrandF.SoL.WangJ.et al (2010). Muscle Injury Activates Resident Fibro/adipogenic Progenitors that Facilitate Myogenesis. Nat. Cel Biol12 (2), 153–163. 10.1038/ncb2015
17
KoleR.KriegA. M. (2015). Exon Skipping Therapy for Duchenne Muscular Dystrophy. Adv. Drug Deliv. Rev.87, 104–107. 10.1016/j.addr.2015.05.008
18
KulkarniS. S.CaryL. H.GamblesK.Hauer-JensenM.KumarK. S.GhoshS. P. (2012). Gamma-tocotrienol, a Radiation Prophylaxis Agent, Induces High Levels of Granulocyte colony-stimulating Factor. Int. Immunopharmacology14 (4), 495–503. 10.1016/j.intimp.2012.09.001
19
Le MoalE.PialouxV.JubanG.GroussardC.ZouhalH.ChazaudB.et al (2017). Redox Control of Skeletal Muscle Regeneration. Antioxid. Redox Signaling27 (5), 276–310. 10.1089/ars.2016.6782
20
LimK.YoonC.YokotaT. (2018). Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy. Jpm8 (4), 38. 10.3390/jpm8040038
21
LiuL.CharvilleG. W.CheungT. H.YooB.SantosP. J.SchroederM.et al (2018). Impaired Notch Signaling Leads to a Decrease in P53 Activity and Mitotic Catastrophe in Aged Muscle Stem Cells. Cell Stem Cell23 (4), 544–556. 10.1016/j.stem.2018.08.019
22
LuA.PoddarM.TangY.ProtoJ. D.SohnJ.MuX.et al (2014). Rapid Depletion of Muscle Progenitor Cells in Dystrophic Mdx/utrophin−/− Mice. Hum. Mol. Genet.23 (18), 4786–4800. 10.1093/hmg/ddu194
23
McGreevyJ. W.HakimC. H.McIntoshM. A.DuanD. (2015). Animal Models of Duchenne Muscular Dystrophy: from Basic Mechanisms to Gene Therapy. Dis. Model. Mech.8 (3), 195–213. 10.1242/dmm.018424
24
NakamuraA. (2019). Mutation-Based Therapeutic Strategies for Duchenne Muscular Dystrophy: From Genetic Diagnosis to Therapy. Jpm9 (1), 16. 10.3390/jpm9010016
25
OguraY.TajrishiM. M.SatoS.HindiS. M.KumarA. (2014). Therapeutic Potential of Matrix Metalloproteinases in Duchenne Muscular Dystrophy. Front. Cel Dev. Bio.2, 11. 10.3389/fcell.2014.00011
26
OuisseL.-H.RemyS.LafouxA.LarcherT.TessonL.ChenouardV.et al (2019). Immunophenotype of a Rat Model of Duchenne's Disease and Demonstration of Improved Muscle Strength after Anti-cd45rc Antibody Treatment. Front. Immunol.10, 2131. 10.3389/fimmu.2019.02131
27
PalauV. E.ChakrabortyK.WannD.LightnerJ.HiltonK.BrannonM.et al (2018). γ-Tocotrienol Induces Apoptosis in Pancreatic Cancer Cells by Upregulation of Ceramide Synthesis and Modulation of Sphingolipid Transport. BMC Cancer18 (1), 564. 10.1186/s12885-018-4462-y
28
PastoretC.SebilleA. (1995). Mdx Mice Show Progressive Weakness and Muscle Deterioration with Age. J. Neurol. Sci.129 (2), 97–105. 10.1016/0022-510x(94)00276-t
29
PehH. Y.TanW. S. D.ChanT. K.PowC. W.FosterP. S.WongW. S. F. (2017). Vitamin E Isoform γ-tocotrienol Protects against Emphysema in Cigarette Smoke-Induced COPD. Free Radic. Biol. Med.110, 332–344. 10.1016/j.freeradbiomed.2017.06.023
30
PerryG.RainaA. K.NunomuraA.WatayaT.SayreL. M.SmithM. A. (2000). How Important Is Oxidative Damage? Lessons from Alzheimer's Disease. Free Radic. Biol. Med.28 (5), 831–834. 10.1016/s0891-5849(00)00158-1
31
PrasadS.GuptaS. C.TyagiA. K.AggarwalB. B. (2016). γ-Tocotrienol Suppresses Growth and Sensitises Human Colorectal Tumours to Capecitabine in a Nude Mouse Xenograft Model by Down-Regulating Multiple Molecules. Br. J. Cancer115 (7), 814–824. 10.1038/bjc.2016.257
32
QaisarR.BhaskaranS.Van RemmenH. (2016). Muscle Fiber Type Diversification during Exercise and Regeneration. Free Radic. Biol. Med.98, 56–67. 10.1016/j.freeradbiomed.2016.03.025
33
SaccoA.MourkiotiF.TranR.ChoiJ.LlewellynM.KraftP.et al (2010). Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice. Cell143 (7), 1059–1071. 10.1016/j.cell.2010.11.039
34
SaheeraS.PotnuriA. G.NairR. R. (2019). Protective Effect of Antioxidant Tempol on Cardiac Stem Cells in Chronic Pressure Overload Hypertrophy. Life Sci.222, 88–93. 10.1016/j.lfs.2019.02.054
35
ScaramozzaA.ParkD.KolluS.BeermanI.SunX.RossiD. J.et al (2019). Lineage Tracing Reveals a Subset of Reserve Muscle Stem Cells Capable of Clonal Expansion under Stress. Cell Stem Cell24 (6), 944–957. 10.1016/j.stem.2019.03.020
36
SeboriR.KunoA.HosodaR.HayashiT.HorioY. (2018). Resveratrol Decreases Oxidative Stress by Restoring Mitophagy and Improves the Pathophysiology of Dystrophin-Deficient Mdx Mice. Oxidative Med. Cell Longevity2018, 1–13. 10.1155/2018/9179270
37
Shimizu-MotohashiY.AsakuraA. (2014). Angiogenesis as a Novel Therapeutic Strategy for Duchenne Muscular Dystrophy through Decreased Ischemia and Increased Satellite Cells. Front. Physiol.5, 50. 10.3389/fphys.2014.00050
38
Shimizu-MotohashiY.KomakiH.MotohashiN.TakedaS. i.YokotaT.AokiY. (2019). Restoring Dystrophin Expression in Duchenne Muscular Dystrophy: Current Status of Therapeutic Approaches. Jpm9 (1), 1. 10.3390/jpm9010001
39
SinghV. K.FatanmiO. O.WiseS. Y.NewmanV. L.RomaineP. L. P.SeedT. M. (2016). The Potentiation of the Radioprotective Efficacy of Two Medical Countermeasures, Gamma-Tocotrienol and Amifostine, by a Combination Prophylactic Modality. Radiat. Prot. Dosimetry172 (1-3), 302–310. 10.1093/rpd/ncw223
40
SinghV. K.WiseS. Y.FatanmiO. O.ScottJ.RomaineP. L. P.NewmanV. L.et al (2014). Progenitors Mobilized by Gamma-Tocotrienol as an Effective Radiation Countermeasure. PLoS One9 (11), e114078. 10.1371/journal.pone.0114078
41
SkukD.TremblayJ. P. (2003). Myoblast Transplantation: the Current Status of a Potential Therapeutic Tool for Myopathies. J. Muscle Res. Cel Motil24 (4-6), 285–300. 10.1023/a:1025425823322
42
SumanS.DattaK.ChakrabortyK.KulkarniS. S.DoironK.FornaceA. J.Jr.et al (2013). Gamma Tocotrienol, a Potent Radioprotector, Preferentially Upregulates Expression of Anti-apoptotic Genes to Promote Intestinal Cell Survival. Food Chem. Toxicol.60, 488–496. 10.1016/j.fct.2013.08.011
43
TanJ.-K.JaafarF.MakpolS. (2018). Proteomic Profiling of Senescent Human Diploid Fibroblasts Treated with Gamma-Tocotrienol. BMC Complement. Altern. Med.18 (1), 314. 10.1186/s12906-018-2383-6
44
TangK.LiuJ.RussellP.ClementsJ.LingM.-T. (2019). Gamma-Tocotrienol Induces Apoptosis in Prostate Cancer Cells by Targeting the Ang-1/Tie-2 Signalling Pathway. Ijms20 (5), 1164. 10.3390/ijms20051164
45
VerhaartI. E. C.Aartsma-RusA. (2019). Therapeutic Developments for Duchenne Muscular Dystrophy. Nat. Rev. Neurol.15 (7), 373–386. 10.1038/s41582-019-0203-3
46
VitielloL.MarabitaM.SoratoE.NogaraL.ForestanG.MoulyV.et al (2018). Drug Repurposing for Duchenne Muscular Dystrophy: The Monoamine Oxidase B Inhibitor Safinamide Ameliorates the Pathological Phenotype in Mdx Mice and in Myogenic Cultures from DMD Patients. Front. Physiol.9, 1087. 10.3389/fphys.2018.01087
47
WangY. X.FeigeP.BrunC. E.HekmatnejadB.DumontN. A.RenaudJ.-M.et al (2019). EGFR-aurka Signaling Rescues Polarity and Regeneration Defects in Dystrophin-Deficient Muscle Stem Cells by Increasing Asymmetric Divisions. Cell Stem Cell24 (3), 419–432. 10.1016/j.stem.2019.01.002
48
WhiteheadN. P.YeungE. W.FroehnerS. C.AllenD. G. (2010). Skeletal Muscle NADPH Oxidase Is Increased and Triggers Stretch-Induced Damage in the Mdx Mouse. PLoS One5 (12), e15354. 10.1371/journal.pone.0015354
49
YamashitaS.BabaK.MakioA.KumazoeM.HuangY.LinI.-C.et al (2016). γ-Tocotrienol Upregulates Aryl Hydrocarbon Receptor Expression and Enhances the Anticancer Effect of Baicalein. Biochem. Biophysical Res. Commun.473 (4), 801–807. 10.1016/j.bbrc.2016.03.111
50
ZainuddinA.ChuaK.-H.TanJ.-K.JaafarF.MakpolS. (2017). γ-Tocotrienol Prevents Cell Cycle Arrest in Aged Human Fibroblast Cells through p16INK4a Pathway. J. Physiol. Biochem.73 (1), 59–65. 10.1007/s13105-016-0524-2
51
ZhangH.RyuD.WuY.GarianiK.WangX.LuanP.et al (2016). NAD + Repletion Improves Mitochondrial and Stem Cell Function and Enhances Life Span in Mice. Science352 (6292), 1436–1443. 10.1126/science.aaf2693
52
ZhaoL.HaJ.-H.OklaM.ChungS. (2014). Activation of Autophagy and AMPK by Gamma-Tocotrienol Suppresses the Adipogenesis in Human Adipose Derived Stem Cells. Mol. Nutr. Food Res.58 (3), 569–579. 10.1002/mnfr.201300157
53
ZhaoL.SonJ. S.WangB.TianQ.ChenY.LiuX.et al (2020). Retinoic Acid Signalling in Fibro/adipogenic Progenitors Robustly Enhances Muscle Regeneration. EBioMedicine60, 103020. 10.1016/j.ebiom.2020.103020
54
ZuoL.PannellB. K. (2015). Redox Characterization of Functioning Skeletal Muscle. Front. Physiol.6, 338. 10.3389/fphys.2015.00338
Summary
Keywords
Duchenne muscular dystrophy, γ-tocotrienol, muscle stem cells, oxidative stress, cellular proliferation
Citation
Yang S, Yang J, Zhao H, Deng R, Fan H, Zhang J, Yang Z, Zeng H, Kuang B and Shao L (2022) The Protective Effects of γ-Tocotrienol on Muscle Stem Cells Through Inhibiting Reactive Oxidative Stress Production. Front. Cell Dev. Biol. 10:820520. doi: 10.3389/fcell.2022.820520
Received
23 November 2021
Accepted
01 March 2022
Published
15 March 2022
Volume
10 - 2022
Edited by
Michael De Lisio, University of Ottawa, Canada
Reviewed by
Osvaldo Contreras, Victor Chang Cardiac Research Institute, Australia
Val Andrew Fajardo, Brock University, Canada
Updates
Copyright
© 2022 Yang, Yang, Zhao, Deng, Fan, Zhang, Yang, Zeng, Kuang and Shao.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Lijian Shao, lshao@ncu.edu.cn
This article was submitted to Stem Cell Research, a section of the journal Frontiers in Cell and Developmental Biology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.