bims-moremu Biomed News
on Molecular regulators of muscle mass
Issue of 2026–03–08
34 papers selected by
Anna Vainshtein, Craft Science Inc.



  1. Am J Physiol Cell Physiol. 2026 Mar 04.
      Muscle stem cells (MuSCs) are essential for muscle regeneration, but their function declines with aging 1-4, neuromuscular disorders5-8 , and non-genetic muscle-wasting conditions9 . Their regenerative capacity is also influenced by environmental factors, including dietary changes such as high-fat diets and diabetes 10-12, impacting their ability to restore muscle integrity. Understanding the mechanisms that regulate MuSC function is thus crucial for developing strategies to preserve muscle health and improve regenerative potential in both physiological and pathological contexts. Recent advances have unveiled a crucial role for mitochondria in controlling MuSC quiescence, fate decisions, and differentiation into myofibers. Several studies have now shown that disruption of mitochondrial function, through genetic or pharmacological means, leads to dysregulation of MuSC functions and impaired myogenic lineage progression. Mitochondrial abnormalities in MuSCs have also been shown to contribute to the loss of regenerative capacity observed in conditions such as aging, sepsis, in myopathies. Together, this evidence and others have sparked great interest for understanding how these organelles regulate MuSC behavior and exploring the therapeutic potential of mitochondria targeted therapies to improve or maintain muscle regeneration. This review aims to provide a comprehensive overview of the role of mitochondria in regulating MuSC quiescence, fate decisions and myogenesis under both normal and diseased conditions. It summarizes current knowledge, highlights existing gaps, and explores emerging areas related to bioenergetic properties and metabolic signaling, mitochondrial network dynamics, quality control, and inter-organelle cross-talk across different MuSC states. It also discusses potential therapeutic strategies targeting mitochondrial function to enhance MuSC regenerative capacity and counteract muscle degeneration.
    Keywords:  Muscle stem cells; metabolism; mitochondrial dynamics; mitophagy; stem cell fate
    DOI:  https://doi.org/10.1152/ajpcell.00027.2026
  2. Nat Immunol. 2026 Mar;27(3): 543-555
      As the actuator of movement and a key regulator of organismal metabolism, skeletal muscle is a site at which inflammatory responses must be carefully calibrated to counteract stressors while preventing protracted functional impairments. Exercise, injury and aging are common forms of stress associated with inflammation; yet the specific inducers and sensors driving such inflammation remain poorly characterized. Multipronged assessment of acute and chronic endurance exercise models uncovered a role for muscle mesenchymal stromal cells in transducing exercise-induced mechanical stress into local inflammatory responses and that the mechanosensitive ion channel Piezo1 is the primary molecular sensor. Mechanosensing by stromal cells is also necessary for appropriately timed inflammatory and myogenic responses to acute muscle injury and is associated with age-related muscle inflammation. These findings highlight sensing of altered tissue stiffness by Piezo1 on muscle mesenchymal stromal cells as a fundamental mechanism of stress-induced immunomodulation in skeletal muscle.
    DOI:  https://doi.org/10.1038/s41590-026-02435-4
  3. Biochem Pharmacol. 2026 Feb 27. pii: S0006-2952(26)00185-1. [Epub ahead of print]248 117854
      The cGAS-STING signaling pathway is a central component of the innate immune system. Skeletal muscle, the body's largest metabolic and endocrine organ, is essential for overall health, and maintaining its homeostasis is critically important. This review systematically elaborates on the central position and "double-edged sword" role of the cGAS-STING pathway in skeletal muscle pathophysiology. We detail how, under various pathological stimuli-such as metabolic stress, physical injury, aging, toxin exposure, and systemic diseases-cytoplasmic DNA accumulation aberrantly activates the cGAS-STING pathway. Excessive activation of this pathway drives chronic inflammation, metabolic disturbances, and induces various forms of programmed cell death and cellular senescence. These effects collectively lead to muscle atrophy, fibrosis, and impaired regeneration. Conversely, during physiological adaptation like exercise training, moderate activation of this pathway can facilitate beneficial metabolic remodeling and muscle fiber type transformation. This article critically assesses current research challenges and limitations, particularly regarding cell specificity, the distinction between physiological and pathological activation, disease heterogeneity, and model systems. It also explores potential therapeutic strategies, supported by molecular docking analyses that predict high-affinity interactions between key inhibitors and cGAS/STING proteins. These include small-molecule inhibitors, intervention with upstream activating signals, lifestyle management, and novel biologics with targeted delivery systems. Ultimately, we emphasize that a deeper understanding and precise modulation of cGAS-STING signaling will open new perspectives and offer a promising translational medicine outlook for preventing and treating a range of refractory muscle diseases.
    Keywords:  Mitochondrial DNA; Skeletal muscle atrophy; Sterile inflammation; Targeted therapy; cGAS–STING
    DOI:  https://doi.org/10.1016/j.bcp.2026.117854
  4. J Appl Physiol (1985). 2026 Mar 02.
      Endurance performance exhibits time-of-day variation in both humans and rodents, peaking in the late active-phase. However, whether the timing of endurance training influences performance adaptations remains unclear. To investigate, female mice were trained 5-d/week for 6-weeks at either ZT13 or ZT22, using treadmill running at 70% of each animal's maximal capacity. Endurance performance was assessed at baseline, week-3, and week-6. Secondary outcomes included blood glucose and lactate, cage activity, body composition, liver and skeletal muscle glycogen content, mitochondrial and contractile protein expression. At baseline, late-active phase (ZT22)-tested mice exhibited significantly higher endurance capacity than early-active phase (ZT13)-tested mice (P<0.05). Following 6 weeks of training, ZT13-trained mice demonstrated a greater rate of improvement, with endurance increasing by 132% (P<0.05), compared to 45% in afternoon ZT22-trained mice. By week 6, performance improved but was similar between groups (P>0.05), despite lower absolute training volumes in the ZT13 group. Both training groups reduced fat-mass (ZT13: -31%,ZT22: -32%; P<0.05 vs. control), with no differences in lean mass, food intake or muscle and liver glycogen content (P>0.05). In skeletal muscle, ZT13-trained mice were associated with increased (P<0.05) COXIV protein expression, citrate synthase activity, and shifts in MyHC isoform expression, without changes (P>0.05) in mitochondrial content. ZT13-training elicited superior performance adaptations despite lower absolute workloads, indicating enhanced training efficiency. These findings identify exercise timing as a biologically relevant factor influencing endurance adaptation and variability in exercise responses.
    Keywords:  Circadian rhythm; Exercise timing; Exercise training; Mitochondrial adaptation; Skeletal muscle
    DOI:  https://doi.org/10.1152/japplphysiol.00608.2025
  5. NPJ Microgravity. 2026 Mar 06.
      The purpose of this study was to determine the extent to which extracellular vesicles (EVs) circulating in blood after exercise training act as an effective mimetic to maintain skeletal muscle mass during unloading and/or accelerate recovery after disuse. Ten healthy males (27.7 ± 7.1 y) were recruited for a 6-week progressive resistance and endurance training program. EVs were isolated from blood before (EVs) or immediately after training (ExerVs). EVs were intraperitoneally injected into male mice (4×; 3 × 108 particles/injection) during 14 days of hindlimb unloading (HU), then the muscles were collected immediately or 7 days after HU. ExerVs did not maintain muscle mass, fiber size (fCSA), or protein synthesis but significantly reduced collagen I during HU. ExerV administration rapidly restored Type I fCSA and capillary quantity concomitant with reduced collagen during the reloading period. Overall, this study demonstrates that ExerVs may represent a novel strategy to preserve skeletal muscle health during disuse.
    DOI:  https://doi.org/10.1038/s41526-026-00582-4
  6. J Clin Invest. 2026 Mar 02. pii: e193797. [Epub ahead of print]136(5):
      The immune system is not only essential for host defense, but it is also involved in tissue maintenance and disease pathogenesis. Macrophages play a key role in tissue repair, fibrosis, and tumorigenesis, but the mechanisms underlying their multifunctionality have not been fully explored. Here, we identified Mrep (Ly6ChiCX3CR1loPDPN+CD9+) as a crucial subset of macrophages for muscle regeneration after muscle injury. Muscle regeneration required Mrep-derived activin A, which was produced via the TLR4/TIR domain-containing adapter-inducing interferon-β/TANK-binding kinase 1/interferon regulatory factor 3/7 signaling pathway in response to muscle injury. Mrep exerted pathological effects by secreting activin A in a model of genetically induced heterotopic ossification (HO), which was suppressed by TLR4 inhibition. Thus, this study elucidates the context-dependent functions of macrophages and the link between injury and HO, suggesting that Mrep is a potential therapeutic target for regenerating muscles and suppressing HO.
    Keywords:  Bone biology; Genetic diseases; Immunology; Innate immunity; Muscle biology; Skeletal muscle
    DOI:  https://doi.org/10.1172/JCI193797
  7. Epigenomics. 2026 Mar 05. 1-17
      Sarcopenia is an age-associated degenerative disorder of skeletal muscle, characterized by the progressive decline in muscle mass and function, which increases the risk of falls, injuries, and accidental death in older adults. Deciphering its pathogenic mechanisms is crucial for advancing early detection, precision prevention, and ultimately improving the quality of life for the elderly population. Increasing evidence suggests that epigenetic regulation plays a central role in driving sarcopenia. DNA methylation, chromatin remodeling, and noncoding RNA regulation collectively accelerate the deterioration of bone and muscle by altering gene expression involved in biosynthesis and metabolism, disrupting protein homeostasis, activating inflammatory pathways, and compromising mitochondrial integrity. This review, which synthesizes the most recent progress in epigenetic research on sarcopenia, uses structured searches of PubMed and Web of Science for studies published from 2014 to the present and emphasizes how these interconnected regulatory networks drive the initiation and progression of the disease. Importantly, we emphasize their translational potential to identify novel biomarkers, enabling early risk stratification and informing the development of targeted therapeutic strategies, thereby laying the groundwork for precision clinical intervention.
    Keywords:  Sarcopenia; biomarkers; epigenetics; muscle atrophy; precision medicine
    DOI:  https://doi.org/10.1080/17501911.2026.2637968
  8. Am J Physiol Cell Physiol. 2026 Mar 02.
      Skeletal muscle regeneration is a dynamic process diurnally regulated by circadian rhythms, which govern key myogenic factors. Previous studies have shown that the timing of muscle injury influences early regeneration outcomes, but it remains unclear whether these effects persist beyond early acute regeneration events. This study investigated whether the time of day at which muscle injury occurs alters post-regeneration outcomes in mice. C57BL/6NCrl mice (n = 80) received bilateral cardiotoxin (CTX) injury to the tibialis anterior (TA) during either the rest phase (ZT2-ZT4) or active phase (ZT14-ZT16), with tissues collected at 7- or 42- days post-injury (DPI). All mice were matched with uninjured controls. Gross functional performance, assessed via rotarod and grip strength testing, demonstrated no differences between rest and active phase injury groups across repeated testing. A series of immunohistological analyses were performed to assess general fiber morphology and markers of regenerative state. Although injury phase had largely no effect on most parameters, myofiber size distributions consistently displayed more smaller fibers in rest phase-injured mice, regardless of sex. While there were notable differences in myosin isoform expression, such trends were observed at both 7 and 42 DPI, suggesting a specific morphological effect of injury timing. These findings indicate that the circadian phase at which skeletal muscle injury occurs causes persistent influence on the size distribution of regenerating myofibers, independent of functional recovery, and highlights the need to consider time-of-day and contribution of post-injury activity as a biological variable in muscle regeneration research.
    Keywords:  Cardiotoxin; Circadian Rhythms; Muscle Injury; Skeletal Muscle Regeneration; Tissue Remodeling
    DOI:  https://doi.org/10.1152/ajpcell.00531.2025
  9. J Biol Chem. 2026 Mar 04. pii: S0021-9258(26)00208-5. [Epub ahead of print] 111338
      The MAPK p38α is associated with skeletal muscle's development, differentiation and functionality. But, as it is overactive in muscle diseases and aging, it was proposed to be a pivotal promoter of these processes as well. It is not clear how p38α is involved in these disparate activities, in particular whether its chronic activation alone is sufficient to cause them. We established a mouse model designed to study the effects of p38α per se in skeletal muscle. p38α activation is achieved by inducible expression, in muscle, of an intrinsically active variant, p38αD176A+F327S. Two weeks following expression muscle degeneration and necrotic changes were observed, accompanied with elevation of p53, caspase 3 and γH2AX; and, intriguingly, suppression of the p38's substrates MK2 and MK3 and its activator MKK6. At later timepoints the tissue recovered, apoptotic markers disappeared, but MK2, MK3 and MKK6 remained suppressed, perhaps as a response that restrains p38α-mediated damage and allows recovery. Induction of p38αD176A+F327S in young mice (2 months old) caused milder effects, but MK2, MK3 and MKK6 were suppressed. The p38αD176A+F327S effects were associated with altered level of ∼2,000 mRNA molecules. For 1,700 genes the effect was transient and for ∼300 constant. Stress-induced activation of p38α in C2C12 myoblasts was also associated with MK2 downregulation, but with constant elevation of apoptotic markers. Thus, chronic activation of p38α per se in skeletal muscle is sufficient to cause damage reminiscent of aging effects, but cannot impose full-scale and lasting aging phenotype. The tissue recovers while suppressing the p38α pathway.
    Keywords:  C2C12 cells; MAPK; MK2; MK3; MKK6; p38α; skeletal muscle
    DOI:  https://doi.org/10.1016/j.jbc.2026.111338
  10. Biomark Insights. 2026 ;21 11772719261427170
       Background: Hypoxia alters skeletal muscle metabolism and function through complex regulatory mechanisms, including exosome-mediated microRNA (miRNA) signaling.
    Objectives: This study profiled exosomal miRNAs from hypoxic human skeletal muscle cells (HSMCs) to explore their roles in hypoxic adaptation.
    Design: Human skeletal muscle cells were cultured under normoxic or hypoxic conditions, and secreted exosomes were isolated for comprehensive molecular profiling. High-throughput miRNA sequencing combined with integrative bioinformatic analyses was used to uncover hypoxia-responsive regulatory networks and key miRNA hubs involved in skeletal muscle adaptation.
    Methods: HSMCs were cultured under normoxic or hypoxic conditions for 24 hours. Exosomes were isolated and characterized by transmission electron microscopy, nanoparticle tracking analysis, and immunoblotting. Exosomal miRNAs (n = 3 per group) were profiled using high-throughput sequencing, followed by differential expression, target prediction, enrichment, and network analyses.
    Results: Isolated exosomes displayed typical morphology (mean size: 82.4 ± 3.2 nm) and expressed markers CD9, CD63, and TSG101. Seventy-four miRNAs were significantly dysregulated under hypoxia (23 upregulated, 51 downregulated; FDR < 0.05, |log2FC| ⩾ 1), including upregulated hsa-miR-210-3p and downregulated hsa-miR-486-5p, hsa-miR-127-3p, and hsa-miR-126-3p. Predicted targets (~2000 genes) included 451 genes differentially expressed in hypoxic versus normoxic skeletal muscle cells. Functional enrichment highlighted cancer-related, MAPK, PI3K-Akt, and HIF-1 signaling pathways, along with muscle differentiation processes. Network analysis identified hsa-miR-20a-5p as a central regulatory hub (46 targets), followed by hsa-miR-24-3p and hsa-miR-152-3p. hsa-miR-24-3p showed the strongest disease associations in the miRNA-disease network.
    Conclusions: Hypoxia induces distinct exosomal miRNA signatures in skeletal muscle, regulating genes involved in differentiation, migration, and stress response. These findings suggest that exosome-mediated miRNA signaling contributes to hypoxia-driven muscle adaptation and intercellular communication.
    Keywords:  exosome; hypoxia; miRNA sequencing; normoxia; skeletal muscle
    DOI:  https://doi.org/10.1177/11772719261427170
  11. Front Endocrinol (Lausanne). 2026 ;17 1769545
      With the continuous rise in the global prevalence of type II diabetes mellitus (T2DM), the associated skeletal muscle complications, including insulin resistance, muscle atrophy, and physical frailty, have garnered increasing attention. Skeletal muscle plays a vital role as a metabolic and endocrine organ and is considered a key factor in the pathological mechanisms of T2DM. Despite significant advances in understanding, the intrinsic molecular mechanisms underlying skeletal muscle dysfunction remain incompletely elucidated. Recent studies have highlighted a significant cellular stress response known as endoplasmic reticulum stress (ERS), which is triggered by hyperglycemia, lipotoxicity, and inflammation, and may serve as a pivotal hub in T2DM pathology. This review narratively examines published articles from the past five years, focusing on experimental studies related to ERS and T2DM myopathy. Comprehensive searches were conducted in electronic databases for journal articles published between 2020 and 2025.This review synthesizes experimental studies to elucidate how ERS disrupts muscle homeostasis via the unfolded protein response (UPR) pathways (PERK, IRE1α, and ATF6) contributing to insulin resistance and activation of protein degradation systems. Consequently, intervention strategies targeting ERS may offer new insights and directions for the prevention and treatment of T2DM-related muscle disorders. This review aims to explore the mechanisms by which ERS contributes to T2DM myopathy, identifying potential therapeutic targets and providing a foundation for future clinical research.
    Keywords:  endoplasmic reticulum stress; insulin resistance; muscle atrophy; therapeutic strategies; type 2 diabetes
    DOI:  https://doi.org/10.3389/fendo.2026.1769545
  12. Physiol Rep. 2026 Mar;14(5): e70790
      Lactate is increasingly recognized as a signaling molecule that modulates muscle plasticity. We examined the effects of oral L-sodium lactate supplementation on skeletal muscle adaptation to chronic neuromuscular electrical stimulation (NMES) in rats. Male Wistar rats received oral lactate or water before either a single NMES session (acute) or repeated sessions over 2 weeks (chronic). We assessed muscle weight, strength, myonuclear-associated protein expression (PCM1), protein synthesis (puromycin incorporation), signaling responses (mechanistic target of rapamycin pathway), and mitochondrial-related protein expression (PGC-1α, OXPHOS, and citrate synthase). The oxidative soleus and glycolytic plantaris muscles were analyzed. Lactate supplementation was associated with greater increases in muscle mass and torque during chronic NMES, particularly in the soleus. PCM1 abundance and myofibrillar puromycin incorporation were higher in the lactate-supplemented group, although there were no significant changes in c-Myc or rpS6. PGC-1α expression was elevated in the plantaris muscle, indicating muscle-type-specific mitochondrial modulation. However, the expression levels of the lactate transporters (MCT1 and MCT4) and GPR81 remained largely unchanged in response to oral lactate. Collectively, these findings suggest that oral lactate is associated with distinct molecular signatures and functional outcomes during chronic NMES in a muscle type-dependent manner, warranting further studies using morphological and muscle-specific functional assessments.
    Keywords:  lactate supplementation; mitochondrial biogenesis; myonuclear; neuromuscular electrical stimulation; protein synthesis
    DOI:  https://doi.org/10.14814/phy2.70790
  13. Nat Aging. 2026 Mar 02.
      Exercise confers cognitive benefits in Alzheimer's disease (AD), yet the underlying mechanisms remain incompletely understood. Skeletal muscle functions as an endocrine organ that secretes myokines which affect the homeostasis of extra-muscular organs, including the brain. Here we found that swimming exercise promotes secretion of skeletal muscle-derived extracellular vesicles (SKM-EVs), which are subsequently taken up via pinocytosis by microglia. Gain-of-function and loss-of-function experiments showed that exercise-induced SKM-EVs induce polarization of disease-associated microglia and enhance the clearance of amyloid-beta plaques. Furthermore, miR-378a-3p was identified as a key microRNA cargo in SKM-EVs, regulating lipid metabolism in disease-associated microglia by targeting p110α. Importantly, administration of extracellular vesicles derived from miR-378a-overexpressing myotubes alleviated cognitive impairment in AD mice. Together, our findings demonstrate that exercise-induced SKM-EVs could serve as a myokine, mediating communication from skeletal muscle to the brain, providing a potential exercise-mimicking therapeutic strategy for AD.
    DOI:  https://doi.org/10.1038/s43587-026-01075-5
  14. J R Soc Interface. 2026 Mar 04. pii: 20250534. [Epub ahead of print]23(236):
      Skeletal muscle regeneration is essential for maintaining muscle health and mobility, making it a key area of research. Common in vivo injury models include cardiotoxin (CTX), freeze-induced (FI) and eccentric contraction (EC) injuries. Despite clear differences in regeneration responses, these variations are often overlooked in experimental design. To address this, we extend a validated computational model to simulate muscle fibre remodelling after CTX, FI and EC injuries and further validate it using literature-derived regeneration metrics. Our analysis reveals that each injury type triggers unique cellular and cytokine interactions that influence regeneration, particularly around 28 days post-injury. EC injury recovery is mainly driven by hepatocyte growth factor (HGF), vascular endothelial growth factor A (VEGF-A) and satellite stem cell (SSC) activity in early stages. FI injuries consistently rely on HGF throughout, with transforming growth factor-β (TGF-β), tumour necrosis factor-α (TNF-α), monocyte chemoattractant protein-1 (MCP-1) and SSCs contributing in later phases. CTX injuries show early TGF-β influence and later roles for SSCs, TNF-α, VEGF-A and fibroblast dynamics. These findings reveal distinct regeneration trajectories across injury models that differ in both mode and severity, highlighting potential molecular and cellular mechanisms that warrant further investigation. Our validated model provides a computational framework for future systematic exploration of how injury severity and other initial conditions independently influence regeneration outcomes, which could inform tailored therapeutic strategies in preclinical studies.
    Keywords:  agent-based model; cytokines; injury; muscle; regeneration
    DOI:  https://doi.org/10.1098/rsif.2025.0534
  15. Cell Death Discov. 2026 Feb 28.
      Botulinum toxin type A (BoNTA) injection into the masseter muscle is widely used for clinical and esthetic purposes. Masseter muscle atrophy is a secondary effect of transient neuromuscular blockade induced by BoNTA. While muscle atrophy has been linked to enhanced ubiquitin-proteasome system activity, leading to increased protein degradation, the role of other catabolic pathways, such as apoptosis and autophagy, remains understudied. In the present study, we evaluated these cellular processes in a mice model of unilateral injection of BoNTA in the masseter muscle, and its relationship with muscle atrophy. Changes in neither molecular markers of apoptosis (cleaved caspase-3, cleaved PARP) nor DNA fragmentation were observed in BoNTA-injected muscles. Conversely, a significant accumulation of the autophagy markers microtubule-associated proteins 1 A/1B light chain 3B (LC3), sequestosome 1 (SQSTM1/p62), and BCL2-associated athanogene 3 (BAG3), along with a reduction in muscle fiber diameter, was observed at 7 days post-BoNTA. These changes were not affected by autophagic flux blockade with chloroquine. Interestingly, LC3 accumulation positively correlates with masseter mass reduction induced by BoNTA. These findings suggest that BoNTA disrupts skeletal muscle homeostasis, promoting atrophy through impaired autophagic activity. Our results not only shed light on the mechanism of BoNTA-induced muscle atrophy but also has broader implications for understanding and potentially treating a range of muscle wasting disorders.
    DOI:  https://doi.org/10.1038/s41420-026-02982-7
  16. J Clin Invest. 2026 Mar 05. pii: e194925. [Epub ahead of print]
      Stem cells are critical for the homeostasis of adult tissues. Thyroid hormone (TH), whose intracellular concentration is increased by type 2 deiodinase (D2), is involved in many functions, but its role in quiescence is unknown. Here we show that D2 marks quiescent stem cells in muscle and skin. Genetic D2-depletion in quiescent muscle stem cells triggers their transition from G0 to a GAlert-like state. This increases the proliferative potential of the stem cells, but impairs their self-renewal capacity, leading to depletion of the stem cell pool and regenerative failure over time. Mechanistically, TH sustains Notch signaling, and active Notch overexpression partially rescues D2-depletion. Transient pharmacological inhibition of D2 accelerates muscle regeneration and skin wound healing by promoting stem cell expansion. In conclusion, we show that D2 is a critical metabolic enzyme in maintaining stem cell quiescence and in regulating self-renewal.
    Keywords:  Endocrinology; Metabolism; Muscle
    DOI:  https://doi.org/10.1172/JCI194925
  17. Physiol Rep. 2026 Mar;14(5): e70797
      While conventional tobacco-cigarette smoking continues to decline, e-cigarette (E-cig) use is rising, yet its physiological consequences remain poorly characterized. Chronic activation of the aryl hydrocarbon receptor (AHR) by tobacco smoke impairs skeletal muscle mitochondrial function. Here, we evaluated whether E-cig vapor elicits AHR activation and mitochondrial dysfunction in skeletal muscle. C2C12 mouse myoblasts were exposed to 1% dimethyl sulfoxide (vehicle), 0.02% tobacco-smoke condensate (TSC), or vape condensate (VC) at 0.006%, 0.06%, and 0.3%. Cell viability, AHR-pathway gene expression (Ahr, Ahrr, Cyp1a1), and mitochondrial respiration were assessed. Male C57BL/6J mice (12-16 weeks; n = 4-5/group) underwent acute 2-h or 4-week exposure to room air, tobacco smoke, or E-cig vapor. Serum cotinine, gastrocnemius AHR-pathway genes, muscle contractility, and mitochondrial function were evaluated. In myoblasts, 0.02% TSC and 0.3% VC upregulated Ahrr and Cyp1a1 (p < 0.0001) and reduced complex I state-3 respiration (p < 0.05) without affecting viability. In mice, acute exposure to tobacco smoke and E-cig vapor significantly increased serum cotinine (p < 0.0001), but only tobacco-smoke activated AHR-pathway. Chronic exposure to tobacco smoke and E-cig vapor reduced mitochondrial complex I and II state-3 respiration (p < 0.05), without altering muscle contractile function. These findings suggest that AHR-independent mechanisms contribute to mitochondrial dysfunction with E-cig vapor exposure.
    Keywords:  E‐cigarette; aryl hydrocarbon receptor; mitochondrial dysfunction; tobacco cigarette
    DOI:  https://doi.org/10.14814/phy2.70797
  18. Am J Physiol Cell Physiol. 2026 Mar 04.
      Children with cerebral palsy (CP) have muscle growth impairments (muscle contractures), altered walking patterns and show markers of inflammation. During muscle repair macrophages coordinate with muscle stem cells-satellite cells (MuSC), which have previously been shown to be altered in abundance and function in children with CP. We investigated: 1) if macrophage populations in contractured muscles of children with CP are similar to typically developing (TD) children with a chronic ACL-tear, and 2) if macrophages, capillaries, MuSC, myonuclei, centrally nucleated fibers were associated with each other, indicative of repair. Thirty-six subjects participated in this study (CP: 11.2 ±0.7 years, 18M/12F, TD: 13.5 ±0.8 years, 3M/3F). Muscle biopsies were obtained during surgical correction for muscle contractures-adductors/ gastrocnemius (CPCon), or vastus lateralis (TD-ACL and CP NonCon). Muscle cross-sections were immunohistochemically labeled for total, anti-inflammatory (M2) macrophages, capillaries, myofiber boundaries, while MuSC abundance, activation and proliferation information were used from a prior study. Macrophage subpopulations in CP Con were similar to TD-ACL muscles. Within CPCon there were positive associations between total, M1 macrophages, and MuSC content (r= 0.54, r=0.70, p<0.05, respectively), but not in the CP NonCon muscles. Centrally-nucleated fibers, myonuclear abundance and MuSC content were also positively associated with each other only in the CPCon muscles (r=0.65, r=0.46, r=0.66, p<0.05, respectively). In TD-ACL injured muscles similar associations were seen between macrophages and MuSC, central nucleation and myonuclear abundance. Collectively, our data suggest that contractured muscles in children with CP may be in a state of repair, similar to ACL-injured TD children.
    Keywords:  cerebral palsy; inflammation; macrophages; muscle stem cells; skeletal muscle
    DOI:  https://doi.org/10.1152/ajpcell.00937.2025
  19. Sci Rep. 2026 Mar 17.
      Sepsis remains a leading cause of mortality and long-term disability, with survivors frequently developing intensive care unit-acquired weakness (ICU-AW) as part of post-intensive care syndrome. To identify a nutritional therapy for ICU-AW, we investigated the mechanisms underlying sepsis-induced skeletal muscle dysfunction using a cecal slurry-induced sepsis mouse model. Although body weight and skeletal muscle mass recovered 14 days after sepsis induction, muscle strength remained impaired, accompanied by persistent mitochondrial abnormalities. Transcriptomic analysis revealed that the pathways termed the 'sirtuin signaling pathway' and 'mitochondrial dysfunction' significantly enriched and Sirt3, a major mitochondrial nicotinamide adenine dinucleotide (NAD⁺)-dependent deacetylase, was downregulated. Biochemical analyses confirmed increased acetylated lysine of mitochondrial proteins in septic muscle tissue. Among these proteins, mass spectrometry detected several proteins in the acetylated band, including multiple complex I subunits. Whether these are direct SIRT3 targets remains to be determined. Knockdown of Sirt3 in C2C12 myotubes impaired mitochondrial respiration, whereas treatment with β-nicotinamide mononucleotide (β-NMN) partially rescued energy production. In vivo, acute-phase administration of β-NMN preserved mitochondrial morphology and skeletal muscle strength without altering muscle mass. These findings demonstrate that sepsis induces mitochondrial dysfunction and persistent muscle weakness associated with Sirt3 downregulation, and highlights β-NMN supplementation as a promising NAD⁺-targeted therapeutic strategy for mitigating ICU-AW.
    Keywords:   β-NMN; Mitochondrial respiration; Sepsis; Sirt3; Skeletal muscle weakness
    DOI:  https://doi.org/10.1038/s41598-026-43172-w
  20. PLoS One. 2026 ;21(3): e0331355
      Fibroblast growth factor 2 (FGF2) is known to play a role in skeletal muscle development and growth. We examined two populations of myogenic precursor cells for their responses to FGF2 in vitro using both extraocular and limb skeletal muscle. Fluorescence-activated cell sorting (FACS) was used to isolate two different populations of myogenic precursor cells, the EECD34 cells (positive for CD34, and negative for Sca1, CD31, and CD45) and PAX7-positive cells, from tibialis anterior and extraocular muscles of mice. These cells were cultured and treated with either proliferation or differentiation media in the absence or the presence of FGF2, followed by assays to determine the effects on proliferation and differentiation. EECD34 cells and PAX7-positive cells from both muscles responded to FGF2 with significantly increased proliferation. Both myogenic precursor cell populations from each muscle type showed increased percentage of desmin-positive mononucleated cells, but decreased rates of fusion into multinucleated myotubes in the presence of FGF2 in this in vitro system relative to control cells. FGF2 has pleiotropic effects on skeletal muscles. Contrary to the literature, FGF2 did not inhibit differentiation, but did appear to decrease fusion into multinucleated myofibers in vitro. Examination of immunostaining for myomerger in differentiating PAX7-positive cells in the presence or absence of FGF2 demonstrated a significant reduction of expression in the presence of elevated FGF2 levels. These results provide a potential mechanism for reduction in myofiber number and size in the extraocular muscles in individuals with Apert syndrome, where FGF receptor 2 mutations maintain the receptor in an activated state resulting in significantly reduced myofiber size.
    DOI:  https://doi.org/10.1371/journal.pone.0331355
  21. NPJ Syst Biol Appl. 2026 Mar 03.
      Starvation induces complex metabolic adaptations in skeletal muscle, a key tissue for maintaining energy homeostasis; however, these adaptations are largely impaired in obesity. How obesity alters global metabolic adaptations to starvation in skeletal muscle remains unclear. Here, we analyzed the metabolic adaptations on a trans-omics scale during starvation in skeletal muscle from wild-type (WT) and leptin-deficient obese (ob/ob) mice. We measured multi-omics data during starvation and constructed global trans-omics networks in WT and ob/ob mice. We found that starvation induces "responsiveness" in WT mice, characterized by increases or decreases in key regulator metabolites, including ATP and AMP, as well as enzyme proteins, leading to global regulation of metabolic pathways, which was lost in ob/ob mice. In contrast, during starvation, ob/ob mice exhibit "difference" in comparison to WT mice, manifested by the persistently elevated expression of metabolic enzymes. These features were similarly found in liver, another key metabolic organ. Thus, global loss of responsiveness and elevated enzyme proteins are systemic features of metabolic dysregulation in ob/ob mice.
    DOI:  https://doi.org/10.1038/s41540-026-00678-3
  22. Biosci Biotechnol Biochem. 2026 Mar 06. pii: zbag033. [Epub ahead of print]
      Using a reporter assay system we screened a library of 472 compounds, and identified 1,25(OH)2D3, all-trans-retinoic acid, 9-cis-retinoic acid, 13-cis-retinoic acid, 17-allylamino-17-demethoxygeldanamycin, cantharidin and magnolol that inhibit FOXO1/3a activity. These compounds suppressed the increase in Atrogin1 gene expression induced by dexamethasone in C2C12 myoblasts. Therefore, these compounds may prevent muscle atrophy by inhibiting FOXO1/3a activity.
    Keywords:  FOXO1/3a; dexamethasone; muscle atrophy; screening; skeletal muscle
    DOI:  https://doi.org/10.1093/bbb/zbag033
  23. Future Sci OA. 2026 Dec;12(1): 2635722
       AIMS: GNE myopathy is a heredity disease of unmet medical need associated with progressive skeletal muscle wasting, atrophy and weakness caused by mutations in the GNE gene. GNE plays a pivotal role in sialic acid production. Sialic acid is a critical part of glycoprotein, ganglioside and glycolipid cell-cell interaction which is necessary for normal skeletal muscle function. Previously we demonstrated safety and efficacy of the GNEwt gene lipoplex in one patient.
    METHODS: We engineered GNEM743T and dual function GNEwt/bi-shRNA plasmids to evaluate GNEM743T specific knockdown and GNEwt expression. Knockdown efficiency, protein expression, and functional rescue were assessed. A dose range study in mice quantified plasmid delivery and human GNE expression in muscle.
    RESULTS: We demonstrate effective plasmid function via knockdown of the GNEM743T gene mutation and concurrent expression of GNEwt gene in a dose dependent manner. Similar in vitro increase in sialic acid production is shown between prior single function plasmid and GNEwt/bi-shRNA-GNEM743T dual function plasmid. Moreover, we demonstrate murine in vivo muscle delivery and expression of GNEwt mRNA from the GNEwt/bi-shRNA-GNEM743T plasmid delivered via DOTAP-Cholesterol lipoplex following intravenous injection.
    CONCLUSION: These results encourage future studies, potentially leading toward clinical testing of GNEwt/bi-shRNA-GNEM743T lipoplex for GNE myopathy.
    Keywords:  GNE; GNE M743T; Plasmid; bi-shRNA; myopathy
    DOI:  https://doi.org/10.1080/20565623.2026.2635722
  24. In Vitro Model. 2026 Feb;5(1): 63-78
       Purpose: Sarcopenia is a skeletal muscle (SKM) condition marked by reduced muscle mass and function and is often observed as a comorbidity with inflammatory conditions.
    Methods: We have developed a defined in vitro functional model to study sarcopenia by incubating human-induced pluripotent stem cell-derived SKM cells with 3 nM TNF-alpha (TNFα) for 96 h. The long-term effects of this treatment were studied for up to 32 days in culture. Muscle function was evaluated by measuring myotube width as well as microcantilever contraction amplitude, force, and fatigue index.
    Results: This model revealed the maintenance of a significant reduction in myotube width for 32 days after TNF-α treatment; moreover, a decrease in myotube contraction amplitude and an increase in fatigue indices were recorded for 32 days. In addition, disease progression and tissue degradation of the sarcopenic conditions were monitored for higher reactive oxygen species production for both acute (day 4) and chronic (day 40) timelines.
    Conclusion: This is the first microphysiological system for sarcopenia evaluation that can be used to evaluate therapeutics. This device can now be combined in a multi-organ microphysiological system to study sarcopenia induced by an inflammatory response from other organs or as a comorbidity in the platform.
    Graphical Abstract: Development of the first defined in vitro functional model of sarcopenia on a microcantilever platform. This study recapitulates physiological signatures of disease progression characterized by loss of muscle mass and function and an increase in reactive oxygen species.
    Keywords:  Microcantilever system; Microphysiological system; Myotubes; Sarcopenia; TNFα
    DOI:  https://doi.org/10.1007/s44164-025-00092-9
  25. Sci Rep. 2026 Mar 02. pii: 7817. [Epub ahead of print]16(1):
      
    Keywords:  Altitude; Diffusion; Exercise; Lung; Modelling; Muscle; O2 transport
    DOI:  https://doi.org/10.1038/s41598-025-32441-9
  26. J Transl Med. 2026 Mar 05.
       BACKGROUND: Sarcopenia is an age-related condition characterized by the progressive decline of skeletal muscle mass and function. Although adiponectin is known for its anti-inflammatory and insulin-sensitizing effects that support muscle regeneration, paradoxically, elevated levels in older adults are linked to decreased muscle mass, strength, and performance. This study aimed to investigate the relationship between adiponectin levels, age, body composition, and functional status in elderly individuals, as well as to perform in vitro analyses of adiponectin resistance.
    METHODS: A cohort of 393 elderly subjects underwent anthropometric, bioimpedance, and functional assessments. Plasma adiponectin levels were measured by ELISA, and AdipoR1/AdipoR2 expression in peripheral blood mononuclear cells (PBMCs) was evaluated. In vitro, human skeletal muscle cells (SkMCs) were exposed to high concentrations (50 µM) of AdipoRon, a dual AdipoR1/AdipoR2 agonist, for 24 and 72 h. Analyses include cell viability, oxidative stress, protein homeostasis, autophagy, proteasome activity, and lipid metabolism.
    RESULTS: In elderly subjects, plasma adiponectin levels negatively correlated with BMI (r =  -0.129; p = 0.03), lean mass (r =  -0.252; p = 0.001), muscle mass (r =  -0.296; p = 0.001), and physical performance (SPPB score; r =  -0.163; p = 0.007). After adjusting for BMI and fat mass, adiponectin levels positively correlated with age (r = 0.281; p = 0.001). AdipoR2 expression in peripheral blood mononuclear cells was inversely associated with both age and adiponectin levels, suggesting adiponectin resistance in aging. In vitro, high dose of AdipoR agonist -AdipoRon exposure leads to oxidative stress, impaired proteostasis, dysregulated lipid metabolism, AdipoR2 receptor downregulation, and reduced cell viability. Together, these findings support a model in which elevated adiponectin in aging reflects adiponectin resistance and cellular stress rather than beneficial adiponectin signaling, contributing to muscle dysfunction.
    CONCLUSIONS: These findings highlight a shift in adiponectin signaling during aging, with the downregulation of AdipoR2 promoting systemic adiponectin resistance. Excessive AMPK activity, in the context of impaired AdipoR2 function, contributes to redox imbalance and metabolic dysfunction in the skeletal muscle, favoring a "senescent-like" phenotype.
    Keywords:  AdipoRon; Adiponectin resistance; Aging; Cellular senescence; Sarcopenia; Skeletal muscle dysfunction
    DOI:  https://doi.org/10.1186/s12967-026-07959-9
  27. Front Pharmacol. 2026 ;17 1753486
       Introduction: Mechanical disuse and hypoxia synergistically worsen muscle atrophy by activating apoptosis, necroptosis, and ER stress pathways. While resveratrol, a natural polyphenol, has shown protective effects in isolated disuse or hypoxia models, its efficacy under combined conditions remains unclear.
    Methods: Male C57BL/6J mice (4 months old) were assigned to ground control or hindlimb unloading (HU) groups under normoxia (21% O2) or hypoxia (15% O2) and treated daily with placebo or resveratrol (20 or 40 mg/kg) for two weeks. Muscle mass, grip strength, cling time, and gene expression of apoptotic, necroptotic, and ER stress markers were assessed.
    Results: HU-hypoxia significantly reduced muscle mass and function, with upregulation of stress-related genes. Resveratrol showed dose-dependent protection: 20 mg/kg modestly reduced atrophy, while 40 mg/kg nearly preserved muscle mass and strength to control levels under both normoxic and hypoxic conditions. To our knowledge, this is the first study to demonstrate protective effects of resveratrol in a combined HU and hypoxia model of muscle atrophy, accompanied by modulation of apoptosis, necroptosis and ER stress related gene expression.
    Conclusion: These results suggest that resveratrol may decrease muscle degradation in fast twitch dominant muscles under combined disuse and hypoxia. However, these results are restricted to gastrocnemius muscle in mice, and further investigations in slow twitch muscles and clinical models are required before clinical relevance can be confirmed. These findings support its potential as a therapeutic agent for muscle loss in clinical and spaceflight settings, warranting further translational research.
    Keywords:  apoptosis; endoplasmic reticulum (ER) stress; hindlimb unloading; muscle atrophy; muscle strength; necroptosis; skeletal muscle
    DOI:  https://doi.org/10.3389/fphar.2026.1753486
  28. Front Pharmacol. 2026 ;17 1663850
       Background: With the global population rapidly aging, the prevalence of sarcopenia, referring to a progressive loss of skeletal muscle mass and strength, is increasing, highlighting the need for effective preventive and therapeutic strategies. In this study, we evaluated the efficacy of Myoki, a synthetic peptide, in muscle atrophy models in vitro, in vivo, and in a human clinical trial.
    Methods: This study evaluated the therapeutic potential of Myoki, a synthetic peptide, in preventing muscle atrophy by assessing its effects in multiple models. In vitro, C2C12 myoblasts were used to evaluate Myoki's impact on cytotoxicity, myotube differentiation, and muscle atrophy in DEX-induced atrophy models, with effects measured by western blot, qRT-PCR, and immunofluorescence. The binding affinity between Myoki and myostatin was further evaluated using surface plasmon resonance (SPR) and confirmed by ELISA-based assays. In vivo, the accelerated aging mouse model (SAMP8) was employed to investigate Myoki's effect on muscle fiber area, collagen deposition, and muscle atrophy markers, with muscle histology, fibrosis, and fluorescence intensities of key proteins assessed via immunofluorescence after 45 weeks of treatment. In the clinical study, a randomized, double-blind, placebo-controlled trial was conducted with 80 patients diagnosed with muscle atrophy, who received Myoki (200 mg/day) or placebo for 12 weeks. Key efficacy endpoints included changes in muscle mass (DEXA), handgrip strength, walking speed (6-m walk test), and serum marker levels, with safety monitored throughout the trial.
    Results: Myoki demonstrated no cytotoxicity up to 500 μM in C2C12 cells and significantly promoted myotube differentiation. In DEX-induced muscle atrophy models, Myoki restored protein synthesis signaling and reduced muscle degradation pathways. In the SAMP8 mouse model, Myoki improved muscle fiber area, reduced collagen deposition, and mitigated muscle fibrosis. In the clinical trial, Myoki supplementation for 12 weeks significantly improved muscle mass, walking speed, and grip strength, along with favorable changes in serum markers related to muscle growth and damage.
    Conclusion: Our results position Myoki as a promising potential candidate for mitigating muscle atrophy, including age-associated muscle loss. These findings support its therapeutic potential for conditions such as sarcopenia, making it a valuable candidate for further clinical exploration.
    Clinical Trial Registration: clinicaltrials.gov, CTRI/2024/01/061919.
    Keywords:  muscle atrophy; muscle hypertrophy; myogenic regulatory factors; myostatin; protein degradation; protein synthesis; sarcopenia
    DOI:  https://doi.org/10.3389/fphar.2026.1663850
  29. J Clin Neuromuscul Dis. 2026 Mar 01. 27(3): 63-81
       ABSTRACT: This update begins with a discussion of treatable lipid storage myopathies associated with the use of sertraline and ranolazine. We then turn to monoclonal gammopathy-associated myopathies including a more recently identified disorder that is also treatment-responsive, monoclonal gammopathy-associated glycogen storage myopathy. Several reports on statins and muscle symptoms, toxic myopathy, and immune-mediated necrotizing myopathy follow. Other autoimmune myopathy topics are highlighted. Then, muscular dystrophies are covered with a focus on dystrophinopathies, limb-girdle muscular dystrophy, and facioscapulohumeral muscular dystrophy. Pompe disease follows with a focus on enzyme replacement therapy data. A short section on congenital myopathies precedes a review of reports on myotonic dystrophies and nondystrophic myotonias.
    Keywords:  MRI; muscular dystrophy; myopathy; myositis; statins; ultrasound
    DOI:  https://doi.org/10.1097/CND.0000000000000559
  30. Ageing Res Rev. 2026 Mar 03. pii: S1568-1637(26)00077-2. [Epub ahead of print] 103085
       BACKGROUND: With an aging population globally, prevention of frailty and sarcopenia will become a public health priority. Growth Differentiation Factor-15 (GDF-15), a stress-responsive cytokine of the TGF-β superfamily, has emerged as a promising biomarker linking mitochondrial dysfunction, cellular senescence, and systemic inflammation to biological and phenotypic aging.
    OBJECTIVES: This systematic literature review systematically synthesizes the clinical evidence on GDF-15 as a biomarker of frailty, sarcopenia, and physical function, highlighting patterns, gaps, and the biological plausibility of its role as a predictive marker and therapeutic target.
    METHODS: Following PRISMA guidelines, we searched CENTRAL, Embase, MEDLINE, and PubMed up to February 2026. Studies involving adult human participants with measured serum GDF-15 levels and assessments of frailty or sarcopenia were included. Data were extracted and grouped thematically by population type, study design, and outcome domains. Narrative synthesis was used to compare findings and explore heterogeneity.
    RESULTS: From 1027 records, 35 studies were included, spanning community-dwelling adults, hospitalized patients, and individuals with cardiovascular, metabolic, gastrointestinal, and respiratory diseases. Elevated GDF-15 levels were consistently associated with poorer physical performance and greater frailty severity. Longitudinal studies suggested predictive value for future functional decline, although associations with sarcopenia were less consistent. Sex-specific variations and methodological heterogeneity, including assay techniques and diagnostic criteria, were key sources of variability. Interventional studies demonstrated limited modulation of GDF-15 levels through physical activity alone.
    CONCLUSIONS: These findings support the integration of GDF-15 into precision geriatric care, though further longitudinal and interventional studies, including those evaluating the incremental value of adding GDF-15 to existing screening tools for frailty, sarcopenia, and functional status, are required to establish its clinical utility.
    Keywords:  Growth Differentiation Factor 15; Physical, function; frailty; sarcopenia, handgrip strength
    DOI:  https://doi.org/10.1016/j.arr.2026.103085
  31. J Cell Mol Med. 2026 Mar;30(5): e71078
      Duchenne muscular dystrophy (DMD) is a severe neuromuscular disorder without an effective cure. Adeno-associated virus (AAV) based gene therapy has improved dystrophin function, with sub-optimal clinical outcomes. We reasoned that a combination of rational engineering of AAV9 capsids modified at the post-translational modification sites, optimal promoter selection, and codon-optimisation of the microdystrophin (μDys) can enhance the AAV9 vector functionality. Our initial promoter screening demonstrated improved dystrophin expression in muscle fibres with a ubiquitous CAG promoter (1.61-fold in CAG vs. MHCK7, p < 0.0001) in mdx mice. We then evaluated two engineered AAV9 capsids (N57Q, K51Q) containing CAG-μDys intramuscularly in vivo, which demonstrated a significant improvement in grip strength 18 weeks after gene therapy. Subsequent evaluation of a codon-optimised microdystrophin transgene under the control of the optimal CAG promoter and capsid (AAV9K51Q) by intramuscular administration revealed enhanced muscle grip strength and dystrophin-glycoprotein complex restoration up to 4 months after gene therapy. Based on the improved performance of AAV9K51Q vectors during intramuscular gene transfer, we performed a systemic administration of these vectors alone, and a comparison with the control group revealed a significantly increased muscle contraction force by 1.6-1.7 fold and a 30%-60% dystrophin restoration in skeletal and cardiac muscles, up to 14 months after gene therapy. Collectively, our study underscores the therapeutic potential of engineered AAV9 vectors for potential clinical application in patients with DMD.
    Keywords:  AAV9; Duchenne muscular dystrophy; codon‐optimised microdystrophin; gene therapy
    DOI:  https://doi.org/10.1111/jcmm.71078
  32. Sci Rep. 2026 Mar 05.
      
    Keywords:  25-Hydroxyvitamin D3 ; Rat; Skeletal muscle fiber type; Vitamin D3
    DOI:  https://doi.org/10.1038/s41598-026-40724-y