bims-mihora Biomed News
on Mitohormesis, repair and aging
Issue of 2026–06–07
eighteen papers selected by
Lisa Patel, Istesso



  1. Aging Cell. 2026 Jun;25(6): e70573
      Mitochondrial dysfunction, impaired proteostasis, and reduced stress resistance and resilience are aging hallmarks. At the core of these hallmarks, the mitochondrial unfolded protein response (mtUPR) is a transcriptional pathway that restores mitochondrial proteostasis in response to proteotoxicity. Although the mtUPR is well studied in invertebrates and cell culture models, how the mtUPR is engaged in aged mammalian tissue is poorly defined. Here, we defined the extent to which repeated physical stress initiates mtUPR transcription in aged mouse skeletal muscle and assessed candidate regulatory mechanisms in vivo. Aged muscle exhibited reduced mitoprotective chaperone and protease availability and greater carbonylation of intermyofibrillar mitochondria relative to young muscle, suggesting diminished proteostatic reserve and increased oxidative burden. Short-term physical stress induced a greater initiation of mtUPR genes in aged muscle than young muscle, coinciding with reduced physiological reserve. Physical stress shifted ATF5 localization from the mitochondria to the nucleus in the muscle of both ages, whereas CHOP mRNA and nuclear localization were selectively elevated in aged muscle. Mechanistically, we show mitochondrial reactive oxygen species (mtROS) contribute to mtUPR initiation in aged skeletal muscle. Using in vivo ChIP-qPCR and in vitro knockdown/inhibition experiments, we provide support for CHOP as a redox-sensitive factor contributing in part to the enhanced mtUPR initiation in aged mouse muscle, potentially linked to JNK signaling. Collectively, these data suggest reduced mitochondrial proteostatic reserve and mtROS signaling in aged muscle contribute to an amplified mtUPR transcriptional response following repetitive physical stress, providing the foundation to explore the mtUPR in mammalian aging.
    DOI:  https://doi.org/10.1111/acel.70573
  2. Curr Alzheimer Res. 2026 May 22.
       BACKGROUND: Mitochondrial dysfunction has gained recognition as a central and early event in the pathophysiology of Alzheimer's disease (AD), extending beyond classical energy failure to encompass complex and dynamic perturbations in organelle homeostasis. Despite extensive focus on amyloid-beta (Aβ) and tau, accumulating evidence implicates mitochondria as both targets and amplifiers of neurodegenerative cascades. This review provides a comprehensive synthesis of the mechanistic roles and therapeutic implications of mitochondrial dysfunction in AD, highlighting recent advances and emerging paradigms that underscore mitochondria as integrative nodes in disease onset, progression, and biomarker discovery.
    MATERIALS AND METHODS: We critically evaluate literature from molecular, cellular, and systemslevel studies-including postmortem brain tissue, transgenic models, and patient-derived cellsfocusing on key domains such as bioenergetic collapse, redox imbalance, mitochondrial dynamics and quality control, Aβ and tau interactions, calcium dysregulation, and apoptosis. Novel mitochondrial mechanisms such as mitochondria-associated membranes (MAMs), mitochondrial unfolded protein response (UPRmt), and mitonuclear communication are discussed alongside recent translational efforts.
    RESULTS: Alzheimer's disease is characterized by widespread mitochondrial abnormalities, including impaired oxidative phosphorylation, increased reactive oxygen species (ROS), disrupted mitochondrial fission/fusion equilibrium, defective mitophagy, and abnormal calcium buffering. Moreover, direct mitochondrial accumulation of Aβ and tau disrupts protein import, respiratory chain integrity, and transport dynamics.
    DISCUSSION: These dysfunctions synergistically activate caspase-mediated apoptotic pathways, exacerbating synaptic loss and neuronal death. Promising therapeutic avenues involve antioxidants, NAD+ precursors, mitophagy modulators, and MAM-targeted strategies. Concurrently, mitochondrial biomarkers such as circulating mtDNA, cytochrome c, and neuroimaging via 31P-MRS or PET are emerging as tools for early diagnosis and disease monitoring.
    CONCLUSION: Mitochondria constitute a mechanistic nexus in AD, bridging upstream pathological triggers with downstream neurodegeneration. Advancing the field will require patient-specific models (e.g., iPSC-derived neurons, brain organoids), a deeper understanding of mitochondrial heterogeneity, and integration of mitochondrial targets into multi-modal therapeutic strategies. Precision mitochondrial medicine holds promise to transform AD management through mechanismbased diagnosis, stratification, and intervention.
    Keywords:  Alzheimer’s disease; amyloid-beta; mitochondrial dysfunction; neurodegenerative cascades; oxidative phosphorylation; reactive oxygen species; transgenic mode.
    DOI:  https://doi.org/10.2174/0115672050433653251208201102
  3. bioRxiv. 2026 May 21. pii: 2026.05.19.726440. [Epub ahead of print]
      Weak inhibition of mitochondrial complex I (mtCI) has been shown to have neuroprotective effects in cellular and animal models of Alzheimer's and Huntington's diseases, at least in part by enhancing mitochondrial biogenesis and function. Mitochondrial dysfunction has also been demonstrated in schizophrenia patients and mouse models of schizophrenia. We tested whether weak inhibition of mtCI would ameliorate mitochondrial and behavioral phenotypes in a mouse model of schizophrenia. In mice with four copies of the Gldc gene, 8 weeks of treatment with the weak mtCI inhibitor, the small-molecule tricyclic pyrone compound CP2, reversed spontaneous alternation deficits in the Y maze, startle habituation deficits, and social novelty deficits in the three-chamber social interaction test. Consistent with the mechanism of action, Western blots revealed that CP2 reverses the reduced expression of PGC-1α, a master regulator of mitochondrial biogenesis, and of the VDAC1, a primary gatekeeper for the exchange of metabolites, ions, and ATP between mitochondria and the cytosol. These findings suggest that the improvement of mitochondrial function may represent a novel strategy to reverse pathophysiological and behavioral deficits in schizophrenia.
    DOI:  https://doi.org/10.64898/2026.05.19.726440
  4. Cell Transplant. 2026 Jan-Dec;35:35 9636897261453307
      Following biomaterial implantation, modulation of the acute immune response is essential for tissue regeneration. Polymorphonuclear leukocytes (PMNs) are critical effector cells in wound healing, and PMN dysfunction is mediated by mitochondrial dysfunction and can lead to prolonged inflammation and tissue damage. It was hypothesized that mitochondrial transplantation could be applied to PMNs in pro-inflammatory states as a means of upregulating regenerative proteins. Primary human PMNs were isolated from donor blood. Isolated PMNs and exogenous mitochondria were co-incubated to induce mitochondrial transplantation. Resulting interactions were assessed through microscopy to confirm initial uptake and mitochondria membrane potential retention, intracellular reactive oxygen species (ROS) analyses (n = 5), and PMN secretome quantification (n = 10) using multiplex protein analysis. Human PMNs were able to successfully uptake delivered mitochondria, and regenerative factors essential for tissue repair and immune cell recruitment including fibroblast growth factor-2 (FGF-2), interleukin (IL)-22, monocyte chemoattractant protein-1 (MCP-1), and granulocyte colony-stimulating factor (G-CSF) were significantly upregulated, indicating that exogenous mitochondria represent promising modulators of PMN function with broad clinical potential.
    Keywords:  host-biomaterial response; immunoengineering; mitochondrial transplantation; polymorphonuclear leukocyte; tissue regeneration
    DOI:  https://doi.org/10.1177/09636897261453307
  5. Protein Sci. 2026 Jul;35(7): e70665
      Mitochondrial protein import is essential for organelle biogenesis and cellular homeostasis. It operates in an environment that is intrinsically shaped by redox chemistry. Mitochondria are major sources of reactive oxygen species (ROS), which arise as by-products of oxidative phosphorylation. Cells therefore maintain sophisticated ROS-handling systems, including compartmentalized antioxidant networks, to balance redox signaling with protection from oxidative stress. Increasing evidence indicates that these redox conditions directly influence mitochondrial protein import at multiple levels. In this review, we provide an overview of ROS production, ROS signaling, and oxidative stress in relation to mitochondrial protein import. We outline the major mitochondrial protein import pathways, and discuss how their activity is modulated by redox-dependent mechanisms. A particular focus is placed on the mitochondrial disulfide relay system of the intermembrane space, which directly couples protein import to redox chemistry through oxidative folding, and how it is influenced by the local redox environment. Collectively, we propose that mitochondrial protein import is partially governed by redox-dependent mechanisms, enabling integration of metabolic state, stress responses, and signaling pathways.
    Keywords:  disulfide relay; mitochondrial protein import; oxidative stress; reactive oxygen species (ROS); redox signaling
    DOI:  https://doi.org/10.1002/pro.70665
  6. Aging Cell. 2026 Jun;25(6): e70578
      Magnesium is traditionally viewed as a permissive electrolyte required for cellular viability. Emerging evidence, however, reveals a more central role for Mg2+ as an active regulator of mitochondrial bioenergetics and metabolic resilience. In this Review, we synthesize recent advances in renal magnesium handling, mitochondrial Mg2+ transport, and MgATP chemistry to propose a unifying framework in which magnesium functions as a bioenergetic checkpoint. At the cellular level, Mg2+ availability specifies the functional pool of ATP, constrains kinase signaling, and stabilizes mitochondrial performance by limiting calcium overload and oxidative stress. At the tissue and organismal levels, disruption of magnesium homeostasis contributes to metabolic inflexibility, insulin resistance, acute kidney injury, and the progressive decline in stress tolerance that accompanies aging. We further discuss how age-associated drift in mitochondrial magnesium may act as a hidden temporal regulator that lowers the threshold for cellular senescence. Finally, we outline emerging therapeutic strategies, including transport-informed and compartment-specific approaches, that move beyond nonspecific supplementation toward precision modulation of magnesium-dependent bioenergetics. Together, this framework positions magnesium as a mechanistic link between mitochondrial function, metabolic disease, and aging, with broad implications for translational intervention.
    Keywords:  aging and senescence; kidney injury; magnesium; metabolic disease; mitochondria
    DOI:  https://doi.org/10.1111/acel.70578
  7. J Mol Cell Cardiol Plus. 2026 Jun;16 100852
      Cardiac aging reflects a convergence of intrinsic molecular damage and maladaptive stress responses that progressively erode myocardial resilience. Accumulating genomic instability, telomere dysfunction, chromatin remodeling, and metabolic dysregulation activate innate immune signaling and cellular senescence across cardiomyocytes, endothelial cells, fibroblasts, and immune cells. At the tissue level, these processes manifest as microvascular rarefaction, fibrosis, hypertrophy, neurovascular uncoupling, and impaired adaptive capacity, creating a substrate that overlaps extensively with cardiomyopathy, heart failure, and atrial fibrillation (AF). Importantly, senescence in the heart is not monolithic. Emerging multi-omics and spatial analyses reveal context-dependent senescence programs, including transient, injury-associated states that support angiogenesis and repair, alongside chronic senescent phenotypes that propagate inflammation and remodeling through the senescence-associated secretory phenotype (SASP). These observations indicate that senescence is not uniformly deleterious but rather comprises functionally heterogeneous responses within the aging myocardium. Non-cell autonomous interactions-spanning cardiomyocyte-fibroblast crosstalk, immune niche signaling, endothelial cell-neuronal axis, and systemic organ-to-heart communication-further amplify or constrain these trajectories. Advances in biomarker discovery, imaging, and circulating epigenetic signatures now enable biological aging of the heart to be quantified beyond chronological aging, although many circulating biomarkers are not cardiac-specific and may also reflect systemic inflammation, fibrosis, frailty, or generalized biological aging. In parallel, preclinical studies demonstrate that senolytic, senomorphic, metabolic, and nutrient-sensing-targeted interventions can partially restore cardiac homeostasis. Together, these insights suggest that cellular senescence may represent a key mechanism and a potentially targetable process in cardiac aging, with important implications for the prevention and treatment of age-related cardiovascular disease.
    Keywords:  Cellular senescence; Heart; SASP; Senolysis
    DOI:  https://doi.org/10.1016/j.jmccpl.2026.100852
  8. Cell Metab. 2026 Jun 02. pii: S1550-4131(26)00184-1. [Epub ahead of print]38(6): 1089-1092
      Mitochondria are classically viewed as a uniform ATP-producing network; however, a growing body of evidence suggests distinct subpopulations exist within tissues and even single cells. Here, I highlight evidence supporting the presence of functionally distinct mitochondria and propose mechanisms by which these subpopulations are formed and regulated.
    DOI:  https://doi.org/10.1016/j.cmet.2026.04.019
  9. Biochem Soc Trans. 2026 Jun 24. 54(6): 651-664
      For decades, the voltage-dependent anion-selective channel (VDAC), formerly known as the mitochondrial porin, was considered a simple pore enabling nearly free permeability across the outer mitochondrial membrane. This simplified view has been progressively dismantled through the discovery of three mammalian isoforms (VDAC1, VDAC2, and VDAC3) with the gradual attribution, often serendipitous, of diverse cellular roles beyond passive metabolite exchange. Recent advances in cryo-electron microscopy have catalyzed a breakthrough in VDAC research. Three converging lines of evidence are reshaping our understanding: (a) high-resolution structures of VDAC within its native protein complexes; (b) discovery of unexpected functions, including phospholipid scrambling and regulation of outer membrane permeabilization through higher-order oligomeric assemblies; and (c) structural determination of VDAC interactions with macromolecules, as well as small-molecule modulators. Collectively, these insights have strengthened the consideration of VDAC as a multifunctional signaling hub and therapeutic target, with emerging small molecules and peptides designed to modulate gating, oligomerization, and interfering with interacting partners. The aim of this review is to summarize current structural, functional, and pharmacological advances in VDAC biology, emphasizing how oligomerization dynamics and isoform specificity orchestrate mitochondrial behavior and offering perspectives on therapeutic strategies for diseases driven by mitochondrial dysfunction.
    Keywords:  bioenergetics; mitochondria; molecular interactions; molecular ultrastructure; voltage-gated channels
    DOI:  https://doi.org/10.1042/BST20250480
  10. Front Immunol. 2026 ;17 1856086
      The host immune response is increasingly recognized as a critical determinant of implant performance and bone regeneration in craniofacial applications. In osteoimmunology, macrophages act as central regulators of the foreign body response by integrating material-derived cues with intracellular signaling pathways that control inflammation and tissue repair. In this context, biomaterials actively regulate the immune microenvironment. However, the integration of biomaterial physicochemical properties with immune signaling and regenerative outcomes remains incomplete. Here, a mechanistic and design-oriented perspective on osteoimmunological processes governing biomaterial-tissue interactions is provided, with a particular focus on macrophage polarization, cytokine signaling networks, and apoptosis pathways involved in bone remodeling. Special attention is given to titanium wear particles as key immunological stimuli that activate macrophages through NF-κB, MAPK, and STAT signaling pathways, as well as emerging mechanisms including inflammasome activation and immunometabolic reprogramming. A unified osteoimmunological framework is introduced that integrates biomaterial physicochemical properties with immune signaling pathways and regenerative outcomes. Within this framework, material-induced modulation of macrophage phenotypes and cytokine profiles is identified as a central design axis controlling the balance between inflammation and regeneration. Emerging immunomodulatory strategies are discussed, including surface nanoengineering, ion-releasing systems, bioactive coatings, and stimuli-responsive biomaterials enabling spatiotemporal control of immune responses. Key limitations, including the oversimplified classification of macrophage phenotypes and the limited translational relevance of in vitro models, are critically addressed. By integrating immunology with materials science, this review outlines design principles for next-generation immuno-instructive biomaterials. This perspective supports the rational design of immuno-instructive biomaterials with predictable regenerative outcomes.
    Keywords:  biomaterials; bone regeneration; cytokine signaling; immunomodulation; innate immunity; macrophage polarization; osteoimmunology
    DOI:  https://doi.org/10.3389/fimmu.2026.1856086
  11. bioRxiv. 2026 May 27. pii: 2026.05.24.727531. [Epub ahead of print]
      In the context of muscle loss, bone repair is impaired, suggesting that muscle derived signals contribute to bone regeneration. However, how muscle surrounding the injury site communicates with the bone repair niche remains unclear. Here we found that CX3CL1 expression was induced in endothelial cells in muscle surrounding a femoral bone injury site. Deletion of Cx3cl1 impaired bone healing, demonstrating a functional role for CX3CL1 in bone repair. A CX3CL1 receptor, CX3CR1, was expressed by PDGFRα⁺ stromal progenitors and lineage tracing showed that CX3CR1 expressing osteoprogenitor lineage cells accumulated at the injury site during repair. PDGFRα⁺ stromal progenitors showed enhanced osteoblastogenesis in response to recombinant CX3CL1. In older mice, local CX3CL1 delivery increased PDGFRα⁺CX3CR1⁺ osteoprogenitor accumulation and improved bone repair. These findings identify a muscle bone signaling pathway in which endothelial CX3CL1 promotes bone repair through CX3CR1 expressing osteoprogenitors.
    DOI:  https://doi.org/10.64898/2026.05.24.727531
  12. bioRxiv. 2026 May 26. pii: 2026.05.25.727505. [Epub ahead of print]
       Background: Cockayne syndrome (CS), primarily caused by autosomal recessive pathogenic variants in ERCC6 (CSB) or ERCC8 (CSA), is a transcription-coupled nucleotide excision repair disorder. CS frequently presents with features similar to primary mitochondrial disease (PMD), including leukodystrophy, lactic acidemia, and skeletal muscle mitochondrial DNA (mtDNA) depletion. How this mitochondrial phenotype arises at the cellular level, and whether it can be pharmacologically targeted, is not yet clear.
    Methods: We characterized mtDNA content, respiratory chain (RC) protein abundance, mitochondrial biogenesis signaling pathways, and oxidative phosphorylation capacity in primary fibroblasts from two siblings with identical compound heterozygous ERCC6 pathogenic variants (c.1526+1G>T; c.2800C>A, p.Pro934Thr) despite marked intrafamilial phenotypic divergence. A combined metabolic stress exposure (galactose, reduced glutamine, and buthionine sulfoximine, (BSO)) which reduced CS cell survival was used to screen for therapeutic leads among twenty-three candidate mitochondrial disease therapeutic compounds. Lead compounds were mechanistically validated at the level of mitochondrial superoxide, total cellular oxidative stress, glutathione, and autophagic flux.
    Results: Patient fibroblasts exhibited several hallmarks of PMD, including reduced mtDNA content, decreased expression of complex I subunit NDUFB8, elevated expression of TOM20 with paradoxically decreased PGC1α suggestive of impaired mitophagic clearance, and decreased mitochondrial respiratory capacity. Under combined metabolic stress, ATP-levels indicative of survival in CS patient fibroblasts selectively collapsed to ∼20% of controls. Five dual-rescue compounds, defined as agents that reproducibly restored ATP-based cell survival in both patient fibroblast lines under stress, were identified, including N -acetylcysteine (NAC), coenzyme Q10 (CoQ10), rapamycin, taurine, and (-)-epicatechin. Mechanistic profiling resolved three functional classes of therapeutic effects in CS cells: (1) upstream mitochondrial reactive oxygen species reduction (NAC, CoQ10); (2) mTORC1 inhibition bypassing defective stress-induced autophagic induction (rapamycin); and (3) extra-mitochondrial improvement in cellular stress resilience ((-)- epicatechin, taurine).
    Conclusions: ERCC6 -based CSB deficiency produced a stress-sensitive and physiologically complex mitochondrial phenotype in patient fibroblasts that was pharmacologically treatable by targeting three mechanistically distinct pathways. Oxidative and broader stress buffering, autophagy modulation via mTORC1 inhibition, and enhanced cellular resilience highlight novel therapeutic opportunities to be advanced to clinical trials in CSB patients.
    DOI:  https://doi.org/10.64898/2026.05.25.727505
  13. Free Radic Biol Med. 2026 May 29. pii: S0891-5849(26)00822-1. [Epub ahead of print]
       SIGNIFICANCE: The circadian ∼24h timing system coordinates physiological and metabolic processes to anticipate daily environmental changes, yet how molecular clock-driven signals interface with redox signalling to shape health across the life course remain incompletely understood. Redox homeostasis encompasses the adaptive maintenance of a biological steady state through the regulation of reduction-oxidation (redox) reactions. Redox reactions are vital in maintaining cellular functions, from regulating cellular proliferation and differentiation to detoxification of harmful substances and metabolic regulation. This adaptive homeostasis allows cells and tissues to transiently adapt to fluctuating levels of internal and external environmental stressors and build stress resilience to potential damaging stimuli. As we age, our baseline stress-protective systems rise, and our cells and tissues lose the ability to transiently and temporally increase their adaptive capacity further, leading to chronic redox shifts in pathophysiological direction and increased susceptibility to disease and frailty.
    RECENT ADVANCES: Here we integrate circadian timing, NRF2 signalling and redox balance into a unified circadian-NRF2-redox axis as a life course framework for maintaining health from development through ageing. We propose that circadian clocks regulate NRF2 activity through rhythmic modulation of various redox-sensitive transcriptional and post-translational co-regulators, kinases and miRNAs, thereby shaping the amplitude and timing of antioxidant and metabolic responses. Conversely, NRF2-driven transcriptional programmes modulate mitochondrial function, glutathione synthesis and xenobiotic defence in a time-of-day manner, reinforcing circadian robustness in tissues with high oxidative flux.
    CRITICAL ISSUES: The bidirectional interplay between circadian clocks and NRF2-driven redox adaptations generates predictable redox oscillations that gate energy metabolism, cellular repair and immune responses, influencing susceptibility to chronic diseases, from metabolic and cardiorespiratory to neurodegenerative diseases and cancer. We review evidence from in vitro and in vivo experimental models and human studies showing that circadian/NRF/redox misalignments, whether from shiftwork, light pollution, irregular sleep or chronic feeding, amplify oxidative stress and diminish adaptive responses, accelerating health decline with age.
    FUTURE DIRECTIONS: We propose that lifestyle interventions that realign circadian timing (consistent sleep/wake or feeding/fasting schedules) and pharmacological strategies that enhance NRF2 activity can restore redox balance and improve disease risk profiles, highlighting a unifying target to predict health trajectories and promote lifelong health. Understanding redox-circadian interactions will help optimise person-centred chronomedicine approaches for advocating preventative health across the life course and for designing smarter therapeutic treatments for redox-based diseases, utilising time-of-day administration of drug treatments and clinical interventions.
    Keywords:  Age-related Diseases; Ageing; Chronodisruption; Chronotherapy; Circadian Clock; Circadian Rhythms; NRF2; Oxidative Stress; Redox Homeostasis; Redox-Circadian Interactions
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.05.318
  14. Ann Plast Surg. 2026 Jun 03.
       BACKGROUND: To our knowledge, no comprehensive review has specifically examined the role of collagen in peripheral nerve regeneration. Peripheral nerve injuries are associated with substantial impairment and incomplete recovery despite advances in microsurgical repair. Outcomes are limited by donor-site morbidity, graft mismatch, and the biological complexity of nerve degeneration and regeneration. Collagen, a major component of the extracellular matrix, plays an important regulatory role in this process and has emerged as a promising biomaterial for nerve repair. This review examines the biological role of collagen in peripheral nerve regeneration and evaluates current collagen-based repair strategies in the literature. The discussion focuses on how collagen helps coordinate regenerative response after injury by shaping the extracellular environment, supporting key cellular interactions, and guiding axonal recovery.
    METHODS: We conducted a literature review of articles on collagen, peripheral nerve regeneration, and nerve repair using the PubMed and Web of Science databases.
    RESULTS: Collagen was found to be a versatile protein that plays an important role in regenerative microenvironments. As a key extracellular matrix component, it supports Schwann cell adhesion, migration, and alignment, helping to organize the extracellular framework that is required for axonal regrowth and remyelination. Dysregulated collagen deposition can contribute to fibrosis, scar formation, neuroma development, and impaired regeneration. Findings suggest that collagen-based conduits, hydrogels, scaffolds, and decellularized nerve grafts can potentially support peripheral nerve repair by recreating key structural and biochemical features. These biomaterials offer advantages such as biocompatibility and biodegradability, though limitations remain in mechanical strength, degradation timing, and effectiveness in larger nerve gaps.
    CONCLUSION: Collagen plays a central role in both native peripheral nerve regeneration and the development of emerging repair technologies. Future advances in collagen-based biomaterials may strengthen clinical translation and improve functional outcomes after peripheral nerve injury.
    Keywords:  Schwann cells; Wallerian degeneration; biomaterial; collagen; extracellular matrix; nerve repair; peripheral nerve regeneration; scaffolds
    DOI:  https://doi.org/10.1097/SAP.0000000000004785
  15. bioRxiv. 2026 May 23. pii: 2026.05.18.725568. [Epub ahead of print]
      Skeletal muscle satellite cells, residing between the myofiber plasma membrane and the surrounding basement membrane, maintain and repair skeletal muscle throughout life. Typically quiescent, satellite cells can transition into a reversible alert state (G Alert ) that primes them for rapid activation to maintain or repair muscle. From G Alert , SCs can either re-enter quiescence or commit to the cell cycle, expand, and differentiate to fuse with existing regenerating myofibers. Exit from quiescence requires extensive post-transcriptional remodeling, including changes in RNA processing and RNA-binding protein activity. We show that TDP-43, an RNA binding protein, is essential for SC maintenance and muscle repair. Conditional deletion of TDP-43 in SCs caused a consistent and progressive loss of G Alert SCs even in uninjured muscle, leading to depletion of the SC pool. TDP-43 haploinsufficiency was sufficient to impair SC maintenance, indicating that both alleles are required. Integrative analysis suggests that TDP-43 supports expression of stress response-associated transcripts during the quiescent-to-G Alert transition, and that failure to mount this response contributes to SC apoptosis. Thus, we identified TDP-43 as a critical regulator of satellite cell survival as satellite cells activate and establish a TDP-43 requirement for maintaining and repairing skeletal muscle.
    DOI:  https://doi.org/10.64898/2026.05.18.725568
  16. Adv Mater. 2026 Jun 03. e19723
      Tissue defect repair is a dynamic process involving inflammation regulation, angiogenesis, organized extracellular matrix assembly, and immune microenvironment homeostasis. Its success critically depends on repair strategies with precise spatiotemporal control. External field-responsive biomaterials (EFRBs), which respond to optical, magnetic, electrical, ultrasonic, and thermal stimuli, have become a research focus in regenerative medicine due to their on-demand activation, unique (bio)physicochemical properties, and ability to modulate immune-related pathways. This review first outlines the dynamic biological requirements of tissue repair, including the immune microenvironment's role, and the core advantages of EFRBs. It then details the structural features and external field response mechanisms of various EFRBs-such as nanoparticles, scaffolds, hydrogels, and microneedles-and their regulatory effects on immune-related repair processes. Finally, it systematically summarizes recent advances in immunoengineering EFRBs for enhancing tissue repair and regeneration. This review thus aims to provide valuable insights for optimizing EFRB-based therapies and to inspire further breakthroughs in this evolving field.
    Keywords:  external field; immune regulation; responsive biomaterials; tissue repair and regeneration
    DOI:  https://doi.org/10.1002/adma.202519723
  17. Mol Biol Rep. 2026 Jun 02. pii: 873. [Epub ahead of print]53(1):
       BACKGROUND: Mitochondrial dysfunction contributes substantially to myocardial ischemia-reperfusion (IR) injury through impaired bioenergetics, oxidative stress, and disruption of mitochondrial homeostasis. MOTS-c, a mitochondrial-derived peptide encoded within the 12 S rRNA region of mtDNA, has been implicated in metabolic stress adaptation, although its role in myocardial IR injury remains incompletely understood.
    METHODS AND RESULTS: Isolated female Wistar rat hearts (n = 6/group) were subjected to 30 min global ischemia followed by 60 min reperfusion using the Langendorff perfusion model. MOTS-c (53 µM) was administered either before ischemia or at reperfusion onset. Cardiac mechanical function, myocardial injury, mitochondrial bioenergetics, oxidative stress, mtDNA copy number, and mitochondrial regulatory gene expression were evaluated in subsarcolemmal and interfibrillar mitochondrial populations. IR significantly impaired cardiac mechanical recovery, increased oxidative stress, reduced electron transport chain and dehydrogenase enzyme activities, disrupted mitochondrial membrane potential, and decreased mtDNA copy number and expression of mitochondrial regulatory genes. MOTS-c treatment improved post-ischemic mechanical recovery, attenuated oxidative stress, partially preserved mitochondrial enzyme activities and membrane potential, and mitigated reductions in mtDNA copy number and mitochondrial gene expression. Protective effects were observed in both mitochondrial subpopulations, although responses varied across parameters.
    CONCLUSIONS: MOTS-c treatment was associated with preservation of mitochondrial functional integrity and improved cardiac recovery following IR injury. These findings support a potential role for mitochondrial-derived peptides in modulating cardiac mitochondrial stress responses during ischemia-reperfusion injury, although the underlying signaling mechanisms require further validation.
    Keywords:  MOTS-c; Mitochondrial bioenergetics; Mitochondrial dysfunction; Mitochondrial subpopulations; Myocardial ischemia-reperfusion injury; Oxidative stress
    DOI:  https://doi.org/10.1007/s11033-026-12064-7