bims-mikwok Biomed News
on Mitochondrial quality control
Issue of 2026–01–04
47 papers selected by
Gavin McStay, Liverpool John Moores University



  1. Int J Mol Sci. 2025 Dec 10. pii: 11907. [Epub ahead of print]26(24):
      Lead (Pb) disrupts mitochondrial function, but its impact on the mitochondrial dynamics and biogenesis during early brain development remains insufficiently understood. This study aimed to investigate the effects of pre- and neonatal Pb exposure on the processes involved in mitochondrial network formation in the brains of rat offspring, simulating environmental exposure. We quantified mRNA expression (qRT-PCR) and protein levels (ELISA) of key mitochondrial fusion (Mfn1, Mfn2, Opa1), fission (Drp1, Fis1) regulators, as well as biogenesis markers (PGC-1α, TFAM, NRF1) in the hippocampus, forebrain cortex, and cerebellum of rats exposed to Pb. Mitochondrial ultrastructure was evaluated using transmission electron microscopy (TEM), and the expression of mitochondrial electron transport chain (ETC) genes was analysed (qRT-PCR). Furthermore, to examine the involvement of the cGAS-STING pathway in Pb-induced neuroinflammation, we measured the expression of ISGs (qRT-PCR), TBK1 phosphorylation (Western blot), and 2',3'-cGAMP synthesis (ELISA). Our results showed that Pb exposure markedly reduced PGC-1α and region-specific NRF1 levels, broadly supressed fusion proteins (Mfn1, Mfn2, Opa1), increased Fis1, and depleted Drp1. ETC gene expression (mtNd1, mtCyb and mtCo1) were upregulated in a brain-structure-dependent manner. These molecular changes were accompanied by pronounced mitochondrial morphological abnormalities. Despite upregulation of Mx1, Ifi44, and Sting1, along with synthesis of 2'3'-cGAMP, TBK1 activation was not detected. All these findings demonstrate that early-life Pb exposure, even low-dose, disrupts mitochondrial biogenesis and the fusion-fission machinery, thus impairs brain energy homeostasis, and implicates mitochondria as central mediators of Pb-induced neuroinflammation and neurodevelopmental toxicity.
    Keywords:  cGAS-STING pathway; developmental lead exposure; lead neurotoxicity; mitochondrial biogenesis; mitochondrial fission/fusion; rat brain
    DOI:  https://doi.org/10.3390/ijms262411907
  2. Int J Mol Sci. 2025 Dec 08. pii: 11852. [Epub ahead of print]26(24):
      Mitochondrial dysfunction is a pivotal contributor to neurodegeneration. Neurons heavily rely on mitochondrial oxidative metabolism and therefore need highly efficient quality control mechanisms, including proteostasis, mitochondrial biogenesis, fusion-fission dynamics, and mitophagy, to sustain bioenergetics and synaptic function. With aging, deterioration of mitochondrial quality control pathways leads to impaired oxidative phosphorylation, excessive reactive oxygen species generation, calcium imbalance, and defective clearance of damaged organelles, ultimately compromising neuronal viability. Pathological protein aggregates, such as α-synuclein in Parkinson's disease, β-amyloid and tau in Alzheimer's disease, and misfolded superoxide dismutase 1 and transactive response DNA-binding protein 43 in amyotrophic lateral sclerosis, further aggravate mitochondrial stress, establishing self-perpetuating cycles of neurotoxicity. Such mitochondrial defects underscore mitochondria as a convergent pathogenic hub and a promising therapeutic target for neuroprotection. Intermediate filaments (IFs), traditionally viewed as passive structural elements, have recently gained attention for their roles in cytoplasmic organization, mitochondrial positioning, and energy regulation. Emerging evidence indicates that IF-mitochondria interactions critically influence organelle morphology and function in neurons. This review highlights the multifaceted involvement of mitochondrial dysfunction and IF dynamics in neurodegeneration, emphasizing their potential as targets for novel therapeutic strategies.
    Keywords:  axonal transport; cell architecture; cell quality; cytoskeleton; mitochondrial dynamics; mitochondrial quality; mitophagy; neurofilaments; neuron; reactive oxygen species
    DOI:  https://doi.org/10.3390/ijms262411852
  3. Respir Res. 2025 Dec 28.
      
    Keywords:  Bronchopulmonary dysplasia; Lung development; Mitochondrial homeostasis; Mitochondrial quality control
    DOI:  https://doi.org/10.1186/s12931-025-03468-3
  4. World J Clin Oncol. 2025 Dec 24. 16(12): 111175
      Sirtuin 3 (SIRT3) is a primary mitochondrial deacetylase. Studies have confirmed that it directly activates mitophagy by modulating mitochondrial protein acetylation. As a key homeostatic mechanism, mitophagy activation alleviates oxidative stress-induced imbalance between cell proliferation and apoptosis, corrects stress-driven mitochondrial metabolic dysfunction, and thus inhibits excessive tumor growth, exerting significant antitumor effects. These functions establish SIRT3 as a key target for regulating mitophagy and cancer therapy. Clinically, strategies centered on its precise regulation may offer a novel direction for gastric cancer (GC) prevention and treatment, with selective activation remaining a critical challenge. SIRT3 could also serve as an auxiliary indicator in clinical guidelines for assessing tumor progression. Given this potential, this mini-review systematically examines SIRT3's mechanisms in regulating mitophagy, its role in GC pathogenesis, and translational prospects for targeting SIRT3 in GC management.
    Keywords:  Antitumor; Gastric cancer; Mitochondrial function; Mitophagy; Oxidative stress; Sirtuin 3
    DOI:  https://doi.org/10.5306/wjco.v16.i12.111175
  5. Foods. 2025 Dec 05. pii: 4173. [Epub ahead of print]14(24):
      Long-term excessive fluoride intake from food causes skeletal fluorosis, which manifests as bone sclerosis, deformation, joint dysfunction, and even disability. Mitophagy and ion homeostasis regulate bone function. This study investigated the role of melatonin (MLT) in mitigating this condition, given its known involvement in bone remodeling and the fact that fluoride impairs its synthesis in the pineal gland. Firstly, network pharmacology and molecular docking identified mitophagy as MLT's key pathway against sodium fluoride (NaF)-induced osteosclerosis. Subsequently, a 400 mg/kg/day body weight NaF exposure model in chicken model with 25 mg/kg/day body weight MLT intervention were established in the current study. Fluoride exposure caused the disturbance of ion homeostasis, and the impairment of mitochondria and activation of PTEN-induced putative kinase1 (PINK1)/E3 ubiquitin ligase Park2 (Parkin)-mediated mitophagy in the bone. Importantly, these deleterious effects were significantly restored by MLT supplementation. In conclusion, NaF causes bone injury via ion homeostasis disruption, osteoblast mitochondrial damage, leading to excessive mitophagy. MLT inhibits fluoride-induced mitophagy through the calcium ion flow-mediated PINK1/Parkin pathway, mitigating bone damage. This study can not only ensure the safety of animal-derived food but also provide a theoretical basis for the prevention and treatment of fluorosis in humans and animals.
    Keywords:  PINK1/Parkin pathway; ion homeostasis; melatonin; mitophagy; skeletal fluorosis
    DOI:  https://doi.org/10.3390/foods14244173
  6. Cell Commun Signal. 2025 Dec 27.
       BACKGROUND: Acute pancreatitis (AP) is a severe inflammatory disorder characterized by pancreatic self-digestion, often progressing to systemic inflammation. Despite advances in understanding its pathogenesis, effective therapeutic strategies remain limited. Heat shock factor 1 (HSF1), a critical transcription factor that maintains cellular homeostasis and regulates the stress response, is downregulated in the pancreas of L-arginine-induced AP mice. However, its role and regulatory mechanisms in the pathogenesis of AP remain unclear. This study aims to elucidate the molecular function and mechanisms of HSF1 in AP, focusing on its regulation by E1A binding protein p300 (EP300) and the downstream effects on mitophagy and inflammation.
    METHODS: Two distinct mouse models of AP were established using L-arginine and cerulein. Pancreatic acinar cells (AR42J) were used to study the effects of HSF1 and parkin RBR E3 ubiquitin protein ligase (PRKN) on mitophagy and inflammation. The expression and regulation between HSF1, PRKN, and EP300 were assessed using genetic and pharmacological approaches.
    RESULTS: HSF1 deficiency exacerbates AP severity in two distinct mouse models, with increased mortality, pancreatic necrosis, and systemic inflammation. Mechanistically, HSF1 directly binds to the promoter of PRKN, enhancing its transcriptional activity. Thus, HSF1 alleviates the inflammatory response in pancreatic acinar cells during AP by promoting PRKN-mediated mitophagy, reducing ROS production, and inhibiting NLRP3 inflammasome activation. HSF1 expression is downregulated in pancreatic acinar cells due to decreased acetylation by EP300, leading to proteasomal degradation and impaired mitophagy. Pharmacological activation of EP300 (e.g., CTB) restores HSF1 expression, enhances mitophagy, and attenuates inflammation in both in vivo and in vitro settings.
    CONCLUSION: These findings highlight the critical role of EP300 in regulating HSF1 acetylation and stability, which in turn modulates mitophagy and pyroptosis in AP. Targeting EP300 and its downstream pathways, such as HSF1-PRKN axis, may offer novel therapeutic strategies for AP.
    Keywords:  Acute pancreatitis; EP300; HSF1; Mitophagy; PRKN
    DOI:  https://doi.org/10.1186/s12964-025-02604-2
  7. Naunyn Schmiedebergs Arch Pharmacol. 2025 Dec 29.
      Radiotherapy is crucial in curative oncology, but normal tissue injuries, such as the kidney, restrict its usage. While rosuvastatin (ROSU) is experimentally known to mitigate renal damage, its potential role in protecting against radiation-induced nephrotoxicity has never been investigated. Accordingly, the current study explored the ROSU's protective impact against radiation-induced nephropathy, with a particular focus on mitophagy regulation. Animals were exposed to 8 Gray (Gy) of whole-body gamma irradiation, either acute or fractionated (2 Gy × 4), and received ROSU (10 mg/kg, i.p.) pre- and post-radiation. Kidney injury was assessed by estimating kidney functions, oxidative stress parameters, and histopathological alterations. To elucidate the mechanism of ROSU, the gene and protein expression of sirtuin 1 (SIRT1) and forkhead box class O (FOXO3a) were estimated, alongside mitophagy and apoptotic biomarkers. Radiation exposure induced cellular necrosis and apoptosis, impaired renal function, and oxidative imbalance. ROSU treatment markedly ameliorated these alterations, demonstrating potent antioxidant activity, as evidenced by reduced malondialdehyde (MDA) level and elevated reduced glutathione (GSH), glutathione peroxidase (GPx), and superoxide dismutase (SOD) levels. Mechanistically, ROSU activated SIRT1 and promoted FOXO3a deacetylation, thereby restoring radiation-impaired mitophagy, as indicated by increased expression of PTEN-induced putative kinase protein 1 (PINK1), Parkinson protein 2 E3 ubiquitin protein ligase (Parkin), and autophagy-related gene 5 (ATG5). This was accompanied by the suppression of intrinsic apoptosis triggered by radiation, as shown by decreased cleaved caspase-3 expression. This study repurposes ROSU in modulating radiation-induced nephropathy, revealing its novel role in redirecting cell fate from apoptosis toward mitophagy through SIRT1/FOXO3a activation.
    Keywords:  Acute irradiation; Apoptosis; Fractionated irradiation; Mitophagy; Nephropathy; Rosuvastatin
    DOI:  https://doi.org/10.1007/s00210-025-04901-6
  8. Lipids Health Dis. 2025 Dec 30.
       BACKGROUND/OBJECTIVES: This study investigated the metabolic and pathological effects of a high-fat diet (HFD) in db/db mice and evaluated the therapeutic efficacy of various Coenzyme Q10 (CoQ10) products. We aimed to determine whether HFD-induced mitochondrial damage can be improved by different CoQ10 products through either repairing mitochondrial injury or increasing mitochondrial bioenergy, thereby addressing the root cause of oxidative stress.
    METHODS AND RESULTS: Plasma biochemical analyses revealed that HFD induced hyperglycemia, elevated hepatic transaminases [aspartate aminotransferase (AST), alanine aminotransferase (ALT)], and dyslipidemia. Lecithin coenzyme Q10 (SoQ10) significantly improved these parameters, especially in reducing AST (255 ± 73.8 U/L vs. 138 ± 29.4 U/L, p < 0.05), ALT (87.8 ± 17.3 U/L vs. 79.2 ± 11.9 U/L, p < 0.05), and triglyceride levels (142.0 ± 37.0 mg/dL vs. 15.5 ± 2.5 mg/dL, p < 0.05), demonstrating greater efficacy than standard CoQ10. Histological evaluation showed that HFD caused marked hepatic steatosis and inflammatory infiltration. Oil Red O staining further confirmed excessive lipid deposition in the livers of HFD-fed mice. Both Q10 treatments decreased lipid droplet accumulation (p < 0.05), with SoQ10 showing a greater reduction (p < 0.05), indicating its potential to alleviate hepatic steatosis. Further assessments indicated that gene expression analyses showed that HFD upregulated lipid metabolism-related genes [lipoprotein lipase (LPL), peroxisome proliferator-activated receptor-γ (PPAR-γ), sterol regulatory element-binding protein-1 (SREBP-1), alkaline ceramidase 2 (ACER2)] (p < 0.05), indicating an imbalance between lipogenesis and lipolysis. SoQ10 modulated these genes and further enhanced ceramide synthase 2 (CERS2) expression, suggesting a role in reestablishing hepatic lipid homeostasis. Additionally, SoQ10 significantly upregulated genes associated with mitochondrial biogenesis peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α), mitochondrial transcription factor A (TFAM)] (p < 0.05) and mitochondrial dynamics [mitofusin-2 (MFN2), optic atrophy type 1 long isoform (OPA1-L)] as well as fission [dynamin-related protein 1 (DRP1), mitochondrial fission protein 1 (Fis1)] (p < 0.05), indicating a potential to restore mitochondrial structural balance. In contrast, conventional CoQ10 had a more limited effect, particularly on fusion-related gene expression.
    CONCLUSIONS: SoQ10 demonstrated superior therapeutic potential over conventional CoQ10 in ameliorating hepatic metabolic dysfunction, oxidative mitochondrial damage, and disturbances in lipid metabolism and mitochondrial dynamics induced by a high-fat diet.
    Keywords:  Coenzyme Q10; Diabetes mellitus; Lipid metabolism; Mitochondrial dysfunction
    DOI:  https://doi.org/10.1186/s12944-025-02835-9
  9. Biomolecules. 2025 Dec 06. pii: 1705. [Epub ahead of print]15(12):
      Traumatic brain injury has long-term detrimental effects on neurological function and general quality of life of affected individuals. Bioenergetic failure is a primary mechanism for cellular dysfunction. We used the mitochondrial activator humanin (HN) to try to normalize the disruptive action of TBI on cellular bioenergetics in the hippocampus. We found that HN supplied right after the injury counteracted the action of TBI on metabolic sensing proteins (LKB1, AMPK, and AKT). HN also counteracted cognitive function and restored the synaptic proteins (Synapsin I and PSD-95) at three weeks post-injury. Moreover, HN normalized the disruptive action of TBI on mitochondrial functioning and dynamics (fusion, fission, and mitophagy). In addition, HN treatment counteracted TBI's effects on mitochondrial biogenesis (PGC-1α), antioxidant (SOD2), and apoptotic marker (CC3). Furthermore, HN intervention in injured animals counteracted the gene expression linked with inflammation (Itgax, SALL1, GFAP, and NLRP3), synaptic plasticity (HDAC2), and bioenergetics (mtND2, TFAM, SIRT1, and SIRT3). These observations emphasize the therapeutic potential of HN by normalizing the fundamental aspects of TBI pathogenesis central to cellular bioenergetics and synaptic plasticity.
    Keywords:  cellular energy; cognition; inflammation; mitochondrial dynamics; traumatic brain injury
    DOI:  https://doi.org/10.3390/biom15121705
  10. Antioxid Redox Signal. 2025 Dec 26.
      Aims: Mitochondrial dysfunction is recognized as a central pathological mechanism in subarachnoid hemorrhage (SAH). This study aimed to investigate whether mitophagy serves as a key mechanism by which hydrogen (H2) exerts its antioxidative effects following SAH. Results: Using in vivo (mouse SAH model) and in vitro (HT22 cell SAH model) approaches, we demonstrated that H2 inhalation significantly improved neurological function and alleviated oxidative stress and apoptosis. Mechanistically, H2 maintained mitochondrial membrane potential and functional integrity by enhancing phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1)/Parkin-mediated mitophagy. RNA sequencing and functional assays identified nuclear factor erythroid 2-related factor 2 (NRF2) as the key upstream target. H2 promoted NRF2 nuclear translocation and activated the antioxidant pathway. Dual-luciferase reporter assays further confirmed that NRF2 directly binds to and activates the PINK1 promoter. Pharmacological inhibition of NRF2 (ML385) or mitophagy (Mdivi-1) abolished the protective effects of H2, confirming that the NRF2-PINK1/Parkin axis is central to the effect of H2. Innovation: The present study clearly establishes the NRF2-PINK1/Parkin axis as a key mechanism underlying the neuroprotective effect of H2 in SAH. This study connects mitochondrial quality control with endogenous antioxidant systems, suggesting H2 administration as a potential mitochondrion-targeted clinical intervention. Conclusion: The NRF2-PINK1/Parkin axis is a novel and key mechanism underlying the neuroprotective effect of H2 in SAH. This finding advances our understanding beyond general antioxidant theories by demonstrating a specific, multistep molecular cascade. H2 administration is a potential mitochondrion-targeted intervention with strong implications for clinical translation in SAH patients. Antioxid. Redox Signal. 00, 000-000.
    Keywords:  early brain injury; hydrogen; mitophagy; nuclear factor erythroid 2-related factor 2; subarachnoid hemorrhage
    DOI:  https://doi.org/10.1177/15230864251410952
  11. Antioxidants (Basel). 2025 Nov 25. pii: 1401. [Epub ahead of print]14(12):
      Ultraviolet radiation B (UVB) radiation can induce oxidative stress, DNA damage, and inflammation, leading to skin wrinkling, impaired barrier function, and an increased risk of cancer. Addressing or preventing photoaging may provide a promising therapeutic avenue for these conditions. Hyperoside (HY), a compound abundantly found in medicinal plants including Hypericum perforatum and Crataegus, has been reported to have various pharmacological activities such as antioxidant, anti-inflammatory, cytoprotective, and antitumor effects; however, there are currently no studies systematically exploring the potential and mechanisms of HY in alleviating skin damage caused by ultraviolet (UV) rays. We investigated the inhibitory effects of HY on oxidative stress responses, reducing keratinocyte aging. HY can also exert these effects by mediating the PI3K/AKT/mTOR signaling pathway through miR-361-5p, maintaining mitochondrial dynamic stability, alleviating mitochondrial dysfunction, and enhancing mitophagy. Additionally, in vivo, HY was able to significantly improve skin wrinkles in mice while reducing changes in thickness and aging of the epidermis and dermis.
    Keywords:  PI3K/Akt/mTOR; hyperoside; miRNA; mitophagy; photoaging
    DOI:  https://doi.org/10.3390/antiox14121401
  12. ACS Chem Neurosci. 2025 Dec 27.
      Parkinson's disease (PD) is a chronic, progressive neurodegenerative disorder characterized by severe motor symptoms. While the degeneration of dopaminergic neurons in the substantia nigra plays a central role, other neurotransmitter systems also contribute to PD symptoms. α-Synuclein (αSyn), normally expressed in neurons to support synaptic function and neurotransmitter release, becomes pathologically accumulated in PD, despite not being upregulated under physiological conditions. Intracellular aggregation of αSyn into Lewy bodies is a hallmark of synucleinopathies. A vital facet of both the onset and progression of PD involves mitochondrial dysfunction, which links αSyn misimport into mitochondria with neuronal death. The interaction of αSyn with mitochondrial membranes has been identified, yet the complex stepwise biological mechanisms of αSyn misimport into the mitochondrial compartments, followed by its aggregation, culminating in mitochondria-mediated apoptosis, remain unknown. The Translocase of the Outer Mitochondrial Membrane (TOM) complex, vital for unidirectional import of >1300 mitochondrial proteins from the cytosol, can additionally misimport αSyn into mitochondria. This TOM-αSyn interplay can alter calcium homeostasis, reduce ATP biogenesis, elevate reactive oxygen species generation, and compromise mitochondrial dynamics, resulting in mitochondrial dysfunction and triggering cell death in dopaminergic neurons. Detailed analyses of TOM complex function, interactome, and TOM-αSyn association could lead to treatment approaches that restore mitochondrial homeostasis by mitigating the effects of αSyn pathology in neurodegenerative conditions. This review details the most recent findings on independent regulators of αSyn and the TOM complex and discusses TOM-αSyn interaction mechanisms and their outcomes on mitochondrial dynamics toward promoting development of therapeutics for neurodegeneration.
    Keywords:  Parkinson’s diseases; TOM complex; aggregation blockers; mitochondrial misimport; neurotoxic plaque; synuclein
    DOI:  https://doi.org/10.1021/acschemneuro.5c00323
  13. Free Radic Biol Med. 2025 Dec 30. pii: S0891-5849(25)01474-1. [Epub ahead of print]
      Sepsis-induced cardiomyopathy (SIC) is a severe complication of sepsis characterized by mitochondrial dysfunction and impaired myocardial contractility, yet its molecular pathogenesis remains incompletely understood. In this study, we demonstrate that excessive mitochondrial fission plays a pivotal role in SIC, contributing to inflammation, oxidative stress, and cardiomyocyte apoptosis. Pharmacological inhibition of mitochondrial fission using Mdivi-1 alleviated these pathological changes both in vivo and in vitro. Bioinformatic analyses of public datasets identified nuclear receptor corepressor 1 (Ncor1) as a key mitochondrial dynamics-related gene upregulated in SIC. Lentiviral knockdown of Ncor1 mitigated myocardial injury and restored mitochondrial homeostasis in both lipopolysaccharide (LPS) and cecal ligation and puncture (CLP) induced SIC mouse model. Mechanistically, we found that the RNA m5C methyltransferase Nsun2 was significantly upregulated in SIC and enhanced Ncor1 mRNA stability via m5C methylation through reading protein ALYREF. Functional experiments revealed that Nsun2 knockdown ameliorated cardiomyocyte injury, while co-knockdown of Ncor1 reversed the deleterious effects of Nsun2 overexpression. Collectively, our findings reveal a novel Nsun2/Ncor1 axis that drives mitochondrial dysfunction in SIC through epi transcriptomic regulation, providing potential therapeutic targets for septic cardiac injury.
    Keywords:  Cardiomyocyte apoptosis; Mitochondrial fission; Ncor1; Nsun2; Sepsis-induced cardiomyopathy (SIC); m5C RNA methylation
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2025.12.056
  14. Pharmacol Res. 2025 Dec 31. pii: S1043-6618(25)00506-7. [Epub ahead of print] 108081
      Bevacizumab is an anti-angiogenic agent widely used in neoadjuvant chemotherapy for advanced triple-negative breast cancer (TNBC). TNBC patients frequently acquire resistance to bevacizumab due to the hypoxic tumor microenvironment, yet the underlying molecular mechanism remains unclear. Here, we demonstrate that mitochondrial reprogramming under hypoxia is crucial for resistance to bevacizumab. Mechanically, prolonged hypoxia causes the glycolytic pathway enzyme PDK1 to accumulate inside mitochondria. In mitochondria, PDK1 exerts its non-canonical function to phosphorylate mitochondrial protein Prohibitin 2 (PHB2) at Ser190. Phosphorylation at Ser190 stabilizes PHB2 and enhances its binding with LC3, thereby initiating mitophagy. Functionally, mitochondrial PDK1 (mito-PDK1) initiates mitophagy in response to hypoxia-induced mitochondrial damage and promotes the malignant phenotype of TNBC cells. In xenograft tumors, inhibiting the function of mito-PDK1 enhances the sensitivity to bevacizumab. Collectively, our findings identify the crucial function and mechanism of mito-PDK1 in TNBC. Targeting mito-PDK1 function may emerge as a novel therapeutic strategy to address acquired resistance to bevacizumab.
    Keywords:  bevacizumab; hypoxia; mitophagy; pyruvate dehydrogenase kinase 1; triple-negative breast cancer
    DOI:  https://doi.org/10.1016/j.phrs.2025.108081
  15. Front Aging Neurosci. 2025 ;17 1692777
      Parkinson's disease (PD) is the selective demise of dopaminergic neurons in the substantia nigra. Conventional neuroprotective strategies based on exogenous antioxidants have shown minimal clinical efficacy. Emerging evidence suggests that neuronal loss in PD may stem not only from direct mitochondrial damage but, more critically, from the failure of an intrinsic "early-warning system"-the mitochondrial retrograde signaling (MRS) pathway-impairing the nucleus's ability to launch timely protective responses. This review repositions pterostilbene, a bioavailable dietary polyphenol, from a simple antioxidant to a "signal fidelity enhancer" that supports mitochondria-to-nucleus communication. By stabilizing mitochondrial function and modulating stress-sensing pathways, pterostilbene may restore MRS integrity and promote activation of endogenous defense mechanisms such as the mitochondrial unfolded protein response (UPRmt). The article advocates a paradigm shift in nutritional neuroprotection: from passive supplementation toward reinforcing the neuron's intrinsic capacity for self-maintenance and resilience.
    Keywords:  Parkinson’s disease; cellular resilience; dopaminergic neurons; mitochondrial retrograde signaling; neuroprotection; polyphenols; pterostilbene
    DOI:  https://doi.org/10.3389/fnagi.2025.1692777
  16. Biol Res. 2025 Dec 27. 58(1): 76
      
    Keywords:   CACNA1A ; Lysosomal dysfunction; Mitochondrial dysfunction; Mitochondrial fission; Mitochondrial fusion; Mitophagy; Molecular mechanisms; Neurodevelopmental disorders
    DOI:  https://doi.org/10.1186/s40659-025-00655-w
  17. Genetics. 2025 Dec 29. pii: iyaf279. [Epub ahead of print]
      Mitochondrial biogenesis requires the import of ∼1,000-1,500 nuclear-encoded proteins across the Translocase of Outer Membrane (TOM) and the Translocase of Inner Membrane (TIM) 22 or 23 complexes. Protein import defects cannot only impair mitochondrial respiration but also cause mitochondrial Precursor Overaccumulation Stress (mPOS) in the cytosol. Recent studies have shown that specific mutations in the nuclear-encoded Adenine Nucleotide Translocase 1 (ANT1) cause musculoskeletal and neurological diseases by clogging TOM and TIM22 and inducing mPOS. Here, we found that overexpression of MFB1, encoding the mitochondrial F-box protein 1, suppresses cell growth defect caused by a clogger allele of AAC2, the yeast homolog of human Ant1. Disruption of MFB1 synergizes with a clogger allele of aac2 to inhibit cell growth. This is accompanied by increased retention of mitochondrial proteins in the cytosol, suggesting exacerbated defect in mitochondrial protein import. Proximity-dependent biotin identification (BioID) suggested that Mfb1 interacts with several mitochondrial surface proteins including Tom22, a component of the TOM complex. Loss of MFB1 under clogging conditions activates genes encoding cytosolic chaperones including HSP31. Interestingly, disruption of HSP31 creates a synthetic lethality with protein import clogging under respiring conditions. We propose that Mfb1 functions to maintain mitochondrial protein import competency under clogging conditions, whereas Hsp31 plays an important role in protecting the cytosol against mPOS. Mutations in DJ-1, the human homolog of Hsp31, and mitochondria-associated F-box proteins (eg., Fbxo7) are known to cause early-onset Parkinson's disease. Our work may help to better understand how these mutations affect cellular proteostasis and cause neurodegeneration.
    Keywords:  DJ-1; F-box protein; Parkinson’s disease; Yeast; chaperone; clogging; mPOS; mitochondria; protein import
    DOI:  https://doi.org/10.1093/genetics/iyaf279
  18. World J Diabetes. 2025 Dec 15. 16(12): 112423
       BACKGROUND: Recent studies have shown that liraglutide, a glucagon-like peptide-1 receptor agonist, has unexpected cardioprotective effects. However, the distinctive effects of liraglutide on diabetic cardiomyopathy (DCM), particularly its effect on mitophagy, have not been fully elucidated.
    AIM: To investigate the effects of liraglutide on cardiac damage and mitophagy in DCM rats.
    METHODS: A high-fat diet and streptozotocin were used to induce DCM in rats. After 12 weeks of liraglutide treatment, rats underwent assessments of cardiac function, serum biochemical parameters, histological changes, apoptosis index, and protein levels. Furthermore, neonatal rat cardiomyocytes (NRCMs) were exposed to 25 mmol/L glucose plus 250 μmol/L palmitate (high glucose + palmitic acid), with or without 200 nmol/L liraglutide, to investigate the effects of liraglutide on cardiomyocyte injury and the underlying mechanisms.
    RESULTS: Liraglutide improved myocardial function and ameliorated cardiac damage in DCM rats, as indicated by reduced myocardial apoptosis, hypertrophy, and interstitial fibrosis (P < 0.05). In NRCMs, Liraglutide alleviated mitochondrial morphological and functional damage as well as oxidative stress, improved mitophagic defects, and reduced cell apoptosis (P < 0.05). Mechanistically, liraglutide alleviated NRCMs damage by enhancing mitophagy mediated by the adenosine monophosphate-activated protein kinase (AMPK)-Parkin signaling pathway, which was evidenced by the reversal of its effects upon compound C treatment.
    CONCLUSION: Liraglutide exerted cardioprotective effects in DCM rats by inhibiting cardiomyocyte apoptosis and promoting mitophagy mediated by the AMPK-Parkin signaling pathway.
    Keywords:  AMPK signaling pathway; Apoptosis; Diabetic cardiomyopathy; Liraglutide; Mitochondria; Mitophagy; Parkin
    DOI:  https://doi.org/10.4239/wjd.v16.i12.112423
  19. Antioxidants (Basel). 2025 Dec 05. pii: 1462. [Epub ahead of print]14(12):
      Cardiovascular diseases (CVDs) remain the leading cause of death worldwide, with a substantial proportion of events occurring prematurely. Atherosclerosis (AS), the central driver of cardiovascular pathology, results from the convergence of metabolic disturbances, vascular inflammation, and organelle dysfunction. Among intracellular organelles, mitochondria have emerged as critical regulators of vascular homeostasis. Beyond their canonical role in adenosine triphosphate (ATP) production, mitochondrial dysfunction-including impaired mitochondrial oxidative phosphorylation (OXPHOS), excessive generation of reactive oxygen species (ROS), accumulation of mitochondrial DNA (mtDNA) damage, dysregulated dynamics, and defective mitophagy-contributes to endothelial dysfunction, vascular smooth muscle cell (VSMC) phenotypic switching, macrophage polarization, and ultimately plaque initiation and destabilization. These insights have established the rationale for mitochondrial "reprogramming"-that is, the restoration of mitochondrial homeostasis through interventions enhancing biogenesis, dynamics, and quality control-as a novel therapeutic paradigm. Interventions that enhance mitochondrial biogenesis, restore mitophagy, and rebalance fission-fusion dynamics are showing promise in preclinical models of vascular injury. A growing array of translational strategies-including small-molecule activators such as resveratrol and Mitoquinone (MitoQ), gene-based therapies, and nanoparticle-mediated drug delivery systems-are under active investigation. This review synthesizes current mechanistic knowledge on mitochondrial dysfunction in ASand critically appraises therapeutic approaches aimed at vascular protection through mitochondrial reprogramming.
    Keywords:  atherosclerosis (AS); endothelial dysfunction; mitochondrial reprogramming; mitophagy; nanoparticle-based therapies; vascular protection; vascular smooth muscle cells (VSMC)
    DOI:  https://doi.org/10.3390/antiox14121462
  20. J Mol Histol. 2025 Dec 29. 57(1): 11
      
    Keywords:  Inflammation; Mitophagy; Nrf2/PINK1/Parkin pathway; Oxidative stress; Shen-Ling-Bai-Zhu-San; Ulcerative colitis
    DOI:  https://doi.org/10.1007/s10735-025-10682-2
  21. Free Radic Biol Med. 2025 Dec 31. pii: S0891-5849(25)01472-8. [Epub ahead of print]
       BACKGROUND: Intestinal ischemia and reperfusion (I/R) injury is a critical pathological condition characterized by the complex interactions among various cell death mechanisms. This study aims to systematically elucidate the regulatory interplay between ferroptosis and mitophagy in intestinal I/R injury, particularly highlighting the pivotal role of the neuronal calcium-binding protein HPCAL1.
    METHODS: Using a mouse intestinal ischemia-reperfusion (I/R) model and a rat small intestinal epithelial cell (IEC-6) hypoxia/reoxygenation (H/R) model, we performed histopathological analysis; Western blotting; co-immunoprecipitation; qPCR; fluorescent probe-based detection; assays for reactive oxygen species and lipid peroxidation; and assessments of mitochondrial membrane potential and autophagic flux. Using these techniques, we examined the time course and features of injury and ferroptosis, mitochondrial dysfunction, and associated molecular regulatory mechanisms.
    RESULTS: The study demonstrated that intestinal ischemia-reperfusion (I/R) injury is significantly time-dependent, peaking at 60 minutes of reperfusion in vivo or 3 hours of reoxygenation in vitro. Key ferroptosis indicators, including increased ACSL4, decreased GPX4 and XCT, GSH depletion, and Fe2+ accumulation, were markedly altered at this peak. Mitophagy inhibition alleviated tissue injury and ferroptosis, indicating excessive mitophagy activation is detrimental. Mechanistically, HPCAL1 was highly expressed at the injury peak. It bound to the mitophagy receptor BNIP3 in a calcium-dependent manner, enhancing BNIP3's stability and interaction with LC3-II, thereby excessively activating mitophagy. This process promoted ferroptosis via a burst of reactive oxygen species (ROS), independent of GPX4 expression changes. Concurrently, the ROS burst activated an Nrf2-mediated compensatory antioxidant response. Disrupting HPCAL1 or BNIP3 effectively broke this cycle, improving cell survival and mitochondrial function.
    CONCLUSION: This study identifies a Ca2+ -mediated HPCAL1-BNIP3 signaling pathway that promotes ferroptosis through ROS-dependent mitophagy activation. It offers novel insights into the mechanisms underlying intestinal ischemia-reperfusion injury and supports the development of therapeutic strategies targeting the critical time window of injury progression as well as specific molecular targets.
    Keywords:  BNIP3; Ferroptosis; HPCAL1; Intestinal Ischemia-Reperfusion Injury; Mitophagy; Reactive Oxygen Species
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2025.12.054
  22. Int J Mol Sci. 2025 Dec 17. pii: 12133. [Epub ahead of print]26(24):
      Growing evidence highlights the links between diabetic neuropathy (DNP), gut dysbiosis, mitochondrial dysfunction and neuroinflammation in colon and bone microstructure deterioration. Geranylgeraniol (GG) shows neuroprotective and osteoprotective capacity. Our study examines GG's effects on pain-associated behaviors, glucose homeostasis, gut microbiota, mitochondrial homeostasis, and bone microstructure in DNP rats. We randomly assigned 27 male Sprague Dawley rats to three groups (n = 8-10/group): a control group (regular low-fat diet), a DNP group (high-fat diet + a single dose of 35 mg/kg streptozotocin), and a GG-treated DNP group (a single dose of 35 mg/kg streptozotocin + GG at 800 mg/kg in diet) for 6 weeks. Nocifensive response was assessed via the von Frey test and an open field test, and the elevated plus maze was used to assess anxio-depressive behaviors. The mRNA expression levels of tight junction protein, mitochondrial homeostasis, and neuroinflammation were measured in the colon using qRT-PCR. We collected fecal samples for microbiota composition analysis with 16S rRNA gene sequencing and analyzed by QIIME 2. All other data were analyzed via one-way ANOVA followed by post hoc Tukey's multiple comparison. p < 0.05 was defined as statistical significance. Our study showed GG's ability to mitigate mechanical hypersensitivity and anxio-depressive behavior in rats with DNP. GG supplementation did not improve glucose homeostasis (i.e., glucose intolerance, insulin sensitivity, pancreatic β-cell dysfunction) and bone microstructure. GG increased alpha-diversity without changing microbial abundance. DNP rats exhibited elevated Clostridium sensu stricto and reduced Eubacterium coprostanoligenes, Lachnospiraceae, Oscillospiraceae, and Peptococcaceae compared with controls. GG did not reverse DNP-induced gut dysbiosis but increased colonic claudin-3 (tight junction), MFN1 (mitochondria fusion), and TFAM (mitochondria biogenesis), while reducing FIS1 (mitochondria fission), GFAP (glial activation), P62 and PINK1 (mitophagy), and TNFα (inflammation). Functionally, GG reduced pain behaviors, improved intestinal integrity and mitochondrial homeostasis, increased alpha-diversity, and suppressed neuroinflammation, but did not improve glucose homeostasis or bone microstructure in obese DNP rats.
    Keywords:  behaviors; brain; diabetic neuropathy; geranylgeraniol; gut microbiome; mitochondria homeostasis; rats
    DOI:  https://doi.org/10.3390/ijms262412133
  23. Exploration (Beijing). 2025 Dec;5(6): 20240129
      Ulcerative colitis (UC) is a chronic and persistent clinical condition that is challenging to cure. Lysine crotonylation (KCr), a recently discovered post-translational modification (PTM), alters protein structure, stability, localization and activity in a variety of processes including cell differentiation and organism development. This study was designed to elucidate the pathophysiological relevance of KCr in UC and uncover potential underlying mechanisms involved. PTM proteomics was employed to track dynamic alterations in KCr sites and protein level in the colon tissue of dextran sulfate sodium (DSS)-induced UC model mice. Following the validation of differentially crotonylated proteins via Western blot assay, functional and mechanistic analyses of specific KCr sites were conducted in vitro. Gain-of-function or loss-of-function mutations were implemented at selected protein KCr sites. The differentially crotonylated proteins including citrate synthetase (CS) between the colon tissue of DSS-induced mice and control mice were predominantly associated with the tricarboxylic acid (TCA) cycle, as evidenced by significant enrichment in the KEGG pathway analysis. These proteins were primarily localized in mitochondria, suggesting a potential link among UC pathogenesis, mitochondria and the TCA cycle. Collectively, increased KCr restricts inflammasome activation by inducing mitophagy, thereby maintaining mitochondrial homeostasis, reducing oxidative stress and inhibiting apoptosis in UC. KCr represents a potential promising therapeutic target for the treatment of UC.
    Keywords:  Citrate synthetase; Lysine crotonylation; Mitophagy; Ulcerative colitis
    DOI:  https://doi.org/10.1002/EXP.20240129
  24. PLoS One. 2026 ;21(1): e0339902
       BACKGROUND: Aerobic exercise promotes mitochondrial morphological, enzymatic, and bioenergetic adaptions to improve muscle health and function. Although moderate intensity continuous training (MICT) is frequently recommended for sedentary and multiple clinical populations, there is little consensus regarding the effects of chronic MICT on these adaptations. The aim of this systematic review and meta-analysis is to evaluate the evidence for the effects of MICT on molecular transducers of mitochondrial biogenesis and cardiorespiratory fitness in adults.
    METHODS: A comprehensive search was conducted in PubMed and CINAHL. Eligible studies assessed MICT lasting ≥2 weeks in adults, published since 2010, and collected vastus lateralis skeletal muscle biopsies pre and post chronic endurance exercise exposure. Data were extracted for mitochondrial transcription factor A (TFAM), citrate synthase (CS), peroxisome proliferator-activated receptor-gamma coactivator 1-alpha (PGC-1α), mitofusin 2 (MFN2), dynamin-related protein 1 (DRP1), VO₂max, and mitochondrial density (MitoVD). Meta-analyses using inverse-variance random effects models were conducted for outcomes reported in at least three studies.
    RESULTS: A total of fourteen studies (n = 184) met inclusion criteria, with an overall low to moderate risk of bias and very low to low certainty of evidence. MICT significantly increased MitoVD (p < 0.00001) and VO₂max (p < 0.0001), while CS (p = 0.05) and MFN2 showed a modest increase (p = 0.01) following MICT. No changes were observed for TFAM, DRP1, or PGC-1α.
    CONCLUSION: MICT significantly improves MFN2 expression, CS activity, MitoVD, and VO2 max in adults. However, the overall quality of evidence is low. Heterogeneity in molecular responses suggests potential moderating effects of training duration, modality (e.g., cycling vs. treadmill), and sex - warranting further research.
    REGISTRATION: PROSPERO ID:CRD42024611640.
    DOI:  https://doi.org/10.1371/journal.pone.0339902
  25. Eur J Med Res. 2025 Dec 30.
       OBJECTIVE: Postoperative cognitive dysfunction (POCD) is a common neurological complication in elderly patients after anesthesia and surgery, and autophagy plays a critical regulatory role in its pathogenesis. This study aimed to systematically clarify the molecular mechanism by which STUB1 mediates POCD in aged mice.
    METHODS: A POCD model in aged mice was established by internal fixation of tibial fracture under anesthesia. Cognitive function was evaluated via conditioned fear test and Morris water maze, and neuronal damage and apoptosis was evaluated through H&E and TUNEL staining. To identify molecular mechanisms, RNA-seq was conducted on the hippocampus, and STUB1/PGC-1α/TFEB axis was identified. STUB1 was knocked out and overexpressed in mouse hippocampal neuron cells (HT22), respectively. The expression of STUB1/PGC-1α/TFEB axis, and the activity of downstream mitophagy, autophagy-lysosome, and apoptosis were investigated both in the hippocampus and neuron cells through qRT-PCR, immunofluorescence, western blot, transmission electron microscope, flow cytometry, and TUNEL staining. PGC-1α ubiquitination was measured through Co-IP.
    RESULTS: Following surgery and anesthesia, the aged mice showed cognitive dysfunction, and neuronal apoptosis, with elevated expression of E3 ubiquitin ligase STUB1, decreased PGC-1α and TFEB expression, and increased PGC-1α ubiquitination in the hippocampus. Moreover, aberrant PINK1/PARKIN-mediated mitophagy, and LAMP-1/LC3/Cathepsin D autophagy-lysosome signaling were found in the hippocampus. In neuron cells, STUB1 overexpression reduced the expression of PGC-1α and TFEB, enhanced PGC-1α ubiquitination, facilitated neuron cell apoptosis, and attenuated mitophagy and autophagy-lysosome pathways.
    CONCLUSION: STUB1 directly binds to PGC-1α and promotes its ubiquitination and degradation, thereby inhibiting the TFEB-dependent autophagy-lysosome pathway and inducing hippocampal neuronal apoptosis, ultimately contributing to POCD in aged mice. This study provides a novel theoretical basis for understanding the pathogenesis of POCD and identifies potential therapeutic targets.
    Keywords:  Autophagy–lysosome pathway; Mitophagy; PGC-1α; Postoperative cognitive dysfunction; STUB1; Ubiquitination
    DOI:  https://doi.org/10.1186/s40001-025-03771-1
  26. Int J Mol Sci. 2025 Dec 12. pii: 11984. [Epub ahead of print]26(24):
      As the central hub of retinal metabolism, mitochondria are vital for sustaining the integrity of the inner blood-retinal barrier (iBRB), which is fundamental to retinal homeostasis. Mitochondrial dysfunction accelerates severe iBRB disruption, a process which is increasingly implicated in a cascade of mitochondrial pathologies including mitochondrial DNA destabilization, oxidative stress, calcium homeostasis disruption, mitochondrial autophagy deficiency, and dysregulated dynamic regulation. This review establishes the iBRB as a crossroads for metabolic, redox, and inflammatory signaling. By analyzing evidence from diabetic retinopathy and retinal vein occlusion models, we clarify how mitochondrial decline translates local energy deficiency into chronic barrier dysfunction. We posit that restoring mitochondrial function is indispensable for vascular resilience and regeneration, a conclusion drawn from integrating molecular, cellular, and translational findings. To advance mitochondrial discoveries into clinical practice, subsequent studies must prioritize achieving spatiotemporally controlled, cell-type-specific interventions with robust in vivo efficacy, thereby successfully translating mitochondrial science into clinical vascular medicine.
    Keywords:  diabetic retinopathy; inner blood-retinal barrier; mitochondrial dysfunction; mitochondrial plasticity; mitochondrial therapy; mitophagy; oxidative stress; retinal vein occlusion
    DOI:  https://doi.org/10.3390/ijms262411984
  27. Clin Exp Hypertens. 2026 Dec 31. 48(1): 2610587
       OBJECTIVE: Perivascular adipose tissue (PVAT) is closely related to the pathogenesis of vascular remodeling in hypertension. The objective of this study was to explore the specific molecular mechanisms underlying the role of PVAT in the onset and progression of hypertensive vascular remodeling.
    METHODS: Thoracic aorta PVAT from male spontaneously hypertensive rats (SHRs) and male Wistar-Kyoto (WKY) rats was used for proteomic analysis, and the differential expression of the identified target proteins was verified by western blotting, immunohistochemistry and transmission electron microscopy (TEM). In vitro, FUN14 domain-containing 2 (FUNDC2) expression was knocked down in 3T3-L1 adipocytes to assess its effects on mitochondrial dynamics, ferroptosis, and adipokine secretion. Next, vascular smooth muscle cells (VSMCs) were cultured in the supernatant of the adipocytes to detect changes in their phenotypic switching and migration.
    RESULTS: The proteomic results revealed that the expression of the outer mitochondrial membrane protein FUNDC2 was significantly upregulated in the PVAT of SHRs. Additionally, the expression of key proteins that regulate mitochondrial dynamics and ferroptosis was altered significantly in the PVAT of SHRs compared with the PVAT of WKY rats. Upon FUNDC2 knockdown in 3T3-L1 adipocytes, proteins related to mitochondrial dynamics, ferroptosis, and adipokines reversed the changes in their expression. Moreover, in VSMCs cultured with the supernatant of FUNDC2-knockdown adipocytes, the VSMC phenotype and migration changed.
    CONCLUSION: Our findings indicated that increased FUNDC2 expression might lead to PVAT dysfunction and abnormal adipokine secretion, potentially through its link to mitochondrial dynamics and ferroptosis in PVAT adipocytes, therefore leading to hypertensive vascular remodeling.
    Keywords:  PVAT; ferroptosis; hypertension; mitochondrial dynamics; vascular remodeling
    DOI:  https://doi.org/10.1080/10641963.2025.2610587
  28. Cell Signal. 2025 Dec 31. pii: S0898-6568(25)00765-X. [Epub ahead of print] 112350
       BACKGROUND: Renal ischemia-reperfusion injury (RIRI) is a major cause of perioperative acute kidney injury and a driver of chronic kidney disease, in which mitochondrial dysfunction and inflammatory activation create a vicious cycle of oxidative stress, inflammation, and tubular cell death. Puerarin, a natural isoflavone with established cardio- and neuroprotective effects, has not been fully evaluated as a modulator of the mitochondrial-immune axis in RIRI.
    METHODS: Network pharmacology and RNA sequencing of mouse kidneys with bilateral RIRI were integrated to identify shared puerarin-RIRI targets and enriched pathways. Molecular docking and 100-ns molecular dynamics simulations were performed to assess puerarin-PI3K binding. In vivo, C57BL/6 mice underwent 45-min bilateral renal ischemia and 24-h reperfusion with or without puerarin pretreatment and/or the PI3K inhibitor LY294002. In vitro, HK-2 cells were subjected to hypoxia/reoxygenation. Renal injury, apoptosis, oxidative stress, inflammatory cytokines, mitochondrial ultrastructure, membrane potential, and mitochondrial dynamics proteins (Drp1, Opa1, Mfn2) were evaluated.
    RESULTS: Network pharmacology and transcriptomics consistently pointed to the PI3K/AKT/NF-κB pathway, which was enriched in oxidative stress, apoptosis, inflammatory signaling, and mitochondrial processes. In both RIRI mice and HR-treated HK-2 cells, puerarin improved renal histology and function, reduced tubular apoptosis and IL-6/IL-1β/TNF-α levels, restored SOD and GSH-Px, lowered ROS and MDA, and preserved mitochondrial membrane potential and ultrastructure. These benefits were accompanied by activation of PI3K/AKT signaling and attenuation of NF-κB, together with normalization of mitochondrial fission-fusion (decreased Drp1, increased Opa1/Mfn2), whereas LY294002 markedly blunted puerarin-induced improvements in mitochondrial dynamics, membrane potential, and injury indices.
    CONCLUSION: Puerarin ameliorates RIRI by activating PI3K/AKT signaling, restoring mitochondrial homeostasis, and attenuating NF-κB-linked inflammatory and apoptotic responses.. These findings support puerarin as a mitochondria- and immune-targeted candidate for perioperative renal protection and justify further translational evaluation.
    Keywords:  Inflammation; Mitochondrial homeostasis; PI3K/AKT/NF-κB pathway; Puerarin; Renal ischemia–reperfusion injury
    DOI:  https://doi.org/10.1016/j.cellsig.2025.112350
  29. J Ethnopharmacol. 2025 Dec 27. pii: S0378-8741(25)01804-5. [Epub ahead of print] 121111
       ETHNOPHARMACOLOGICAL RELEVANCE: Pathological mitochondrial hyperfission and ectopic lipid deposition in renal tubules are critical contributors to the progression of diabetic kidney disease (DKD), with SUMO1-mediated modification of DRP1 functioning as a key driving mechanism. The traditional Chinese medicine formula Suoquan Yishen Formula (SQYSF) has demonstrated clinical efficacy in ameliorating DKD; however, it remains unclear whether it improves the mitochondrial-lipid metabolism network by modulating this post-translational modification.
    AIM OF THE STUDY: This study aimed to elucidate the molecular mechanism by which SQYSF alleviates renal tubular ectopic lipid deposition in DKD by targeting UBC9-mediated DRP1-SUMO1 modification.
    MATERIALS AND METHODS: The therapeutic effects of SQYSF on renal function, lipid deposition, mitochondrial morphology, and SUMOylation were systematically assessed in db/db mice and in HK-2 cells stimulated with high glucose and high fat. Evaluations were performed using histopathological staining, transmission electron microscopy, MitoTracker Red fluorescence staining, Western blotting, co-immunoprecipitation (Co-IP), and cellular thermal shift assays. Functional validation was further conducted using the DRP1 inhibitor Mdivi-1 and the UBC9 inhibitor 2-D08.
    RESULTS: In vivo experiments demonstrated that SQYSF significantly improved renal dysfunction and histopathological injury in DKD mice, accompanied by notable reductions in mitochondrial damage and ectopic lipid deposition. In vitro mechanistic studies showed that SQYSF specifically suppressed both the mRNA and protein expression of the SUMO E2 ligase UBC9, thereby decreasing DRP1-SUMO1 modification. This inhibition downregulated key mitochondrial fission regulators (DRP1, MFF, and FIS1) while concomitantly upregulating essential fatty acid β-oxidation enzymes (CPT1A and CPT2), ultimately leading to reduced lipid accumulation.
    CONCLUSION: This study demonstrates that SQYSF ameliorates DKD by targeting the UBC9-mediated DRP1-SUMO1 modification axis, thereby suppressing pathological mitochondrial fission and reducing ectopic lipid deposition in renal tubules. These findings offer new mechanistic insight and highlight a promising therapeutic strategy for DKD management using traditional Chinese medicine.
    Keywords:  DRP1 SUMOylation; Diabetic kidney disease; SUMO1 modification; Suoquan Yishen Formula; ectopic lipid deposition; pathological mitochondrial hyperfission
    DOI:  https://doi.org/10.1016/j.jep.2025.121111
  30. Stem Cell Reports. 2025 Dec 26. pii: S2213-6711(25)00355-8. [Epub ahead of print] 102751
      In chronic myeloid leukemia (CML), disease persistence in patients is maintained by leukemic stem cells (LSCs), which drive tyrosine kinase inhibitor (TKI) resistance. Autophagy has been proposed as a potential therapy to eradicate CML LSCs. Here, using a small-molecule inhibitor of Hsp70 (heat shock protein 70)-Bim (Bcl-2-interacting mediator of cell death) interaction, S1-10, we demonstrate that Hsp70-Bim is a target for CML stemness maintenance. Hsp70-Bim is driven by Bcr-Abl and mediates particularly stronger mitophagy in CML LSCs than differentiated CML cells and HSCs. The more selective mitophagy regulation of Hsp70-Bim than ULK1 (unc-51-like autophagy activating kinase 1) is illustrated. Pharmacological inhibition of Hsp70-Bim blocks mitophagy, leading to the differentiation of CML LSCs, loss of quiescence, and loss of LSC self-renewal potential. In the patient-derived xenograft (PDX) CML models, S1g-10 reduces the number of LSCs by more than 80% after two weeks of injection, without obvious toxicity on normal red blood cells.
    Keywords:  Hsp70-Bim; chronic myeloid leukemia; leukemia stem cells; mitophagy; tyrosine kinase inhibitor
    DOI:  https://doi.org/10.1016/j.stemcr.2025.102751
  31. Acta Naturae. 2025 Oct-Dec;17(4):17(4): 64-71
      Mitochondrial dysfunction is one of the pathogenetic mechanisms of neuronal damage during aging. The high energy dependence of neurons makes them particularly vulnerable to age-related changes accompanied by oxidative stress and impaired energy metabolism. The maintenance of a pool of functional mitochondria is regulated by mitophagy, which ensures the utilization of damaged organelles, thereby preventing the progression of mitochondrial dysfunction. Brain aging is accompanied by a reduced level of activity of metabolic processes, aggravated mitochondrial dysfunction, and an increased risk of developing neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. This review highlights the molecular and signaling pathways of mitophagy and its dysregulation during physiological and pathological aging, which is of particular interest for identifying pharmaceutical targets and developing potential therapies for neurodegenerative conditions.
    Keywords:  Alzheimer’s disease; Parkinson’s disease; aging; mitochondria; mitophagy
    DOI:  https://doi.org/10.32607/actanaturae.27674
  32. Cell Death Discov. 2025 Dec 30.
      Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal type of cancer with poor diagnosis and prognosis, and overcoming gemcitabine-resistant (Gem-R) is a major obstacle in its treatment. Given the important role of glutamine (Glu) metabolism in tumor drug resistance, we investigated the role and exact mechanism of transglutaminase type 2 (TGM2) in influencing PDAC sensitivity to gemcitabine. In this study, we found that TGM2 exhibited elevated expression levels in Gem-R cells and tissue samples from patients with clinically resistant PDAC. Mechanistically, downregulation of TGM2 suppressed the proliferation of Gem-R PDAC cells both in vitro and in vivo by modulating Glu metabolism. RNA sequencing analysis revealed that the mechanism by which targeting TGM2 inhibits drug resistance in Gem-R PDAC cells may be associated with purinergic receptor P2X7 (P2RX7) within the GO:0014049 pathway (positive regulation of glutamate secretion). P2RX7 is highly expressed in Gem-R PDAC cells and tissue samples, and it participates in Glu metabolism and mitophagy in Gem-R PDAC cells. Furthermore, Glu has also been found to induce mitophagy. Lastly, TGM2 and P2RX7 form a positive feedback regulatory loop, jointly regulating Glu metabolism and mitophagy, thereby promoting drug resistance in Gem-R PDAC cells. These data suggest that the TGM2-P2RX7 loop promotes Gem-R in PDAC by improving Glu metabolism and mitophagy, highlighting its potential as a crucial therapeutic target for PDAC.
    DOI:  https://doi.org/10.1038/s41420-025-02922-x
  33. Transplant Cell Ther. 2025 Dec 25. pii: S2666-6367(25)02649-1. [Epub ahead of print]
      Chimeric antigen receptor (CAR) T cell persistence with memory is the current research focus of cancer immunotherapy. The incomplete effect of CAR T cells against tumors results from CAR T cell dysfunction and exhaustion. Asymmetric cell division is an evolutionarily conserved mechanism to maintain mother stem cells during embryonic development, and for immune cells to provide a continuous supply of diverse populations to fight infections and cancer. CAR T cells use ACD to determine their fate during the first mitotic division after interaction with its target, creating a pool of memory CAR T cells which can be recalled to be effector cells during tumor relapse, necessarily to offset the diminished ability of exhausted CAR T cells in controlling the tumor. Affinity of the CAR T - target cell immune synapse and mitochondrial dynamics regulate ACD. We review the literature regarding CAR T cell persistence, exhaustion, and mechanisms of reversing exhaustion. Subsequently, we present a hypothesis linking mitophagy to CAR T cell exhaustion, modulation of which may be clinically relevant in the treatment of cancers with CAR T cells.
    Keywords:  Asymmetric cell division; CAR T cells; Exhaustion; Memory; Mitophagy; Persistence; T cells
    DOI:  https://doi.org/10.1016/j.jtct.2025.12.988
  34. Circ Res. 2025 Dec 29.
       BACKGROUND: Pathological cardiac hypertrophy, an abnormal enlargement of cardiomyocytes and interstitial fibrosis in response to sustained injury or pressure overload, may lead to heart failure or even sudden death. Affected patients often also exhibit myocardial mitochondrial dysfunction and associated structural damage. Discovering more potent mitochondrial-targeting compounds may therefore hold great benefit, both for elucidating the mechanisms of cardiac hypertrophy and for treating affected patients.
    METHODS: A series of novel 1-deoxynojirimycin (DNJ) derivatives was designed based on the unique binding mode of DNJ with OPA1 (optic atrophy 1). Two-step phenotypic screening was then performed using patient-specific cytoplasmic hybrid cells and iPSC-derived cardiomyocytes to identify promising candidates. Molecular dynamics simulations, combined with proteomic, biochemical, and physiological assays, were used to assess potential therapeutic mechanisms for mitochondrial disorders. OPA1 mutant cell lines were established to test candidate compound target specificity. Pathological cardiac hypertrophy models were established in mice and rats through angiotensin II induction and abdominal aortic constriction, enabling comprehensive evaluation of the candidates' preventive and therapeutic efficacy.
    RESULTS: DNJ occupies a cavity formed by the GTPase domain of the OPA1 dimer, acting as an additional linker at the dimeric OPA1 interface. Here, we have designed and identified a novel DNJ derivative, DNJ5a. Compared with DNJ, DNJ5a exhibits enhanced in silico and in vitro binding specificity, providing additional anchor sites for direct OPA1 interaction. This interaction facilitates the stabilization of the OPA1 dimeric form to repair mitochondrial cristae damage and maintain inner membrane integrity. Comprehensive improvements in mitochondrial bioenergetics, Ca2+ homeostasis, mitophagy, and multidimensional functional responses are seen to result. In 2 rodent animal cardiac hypertrophy models, DNJ5a administration showed excellent preventive and therapeutic efficacy towards promoting mitochondrial health and cardiac function in vivo.
    CONCLUSIONS: Unlike conventional mitochondrial drugs, which act to alleviate symptoms, DNJ5a can specifically target OPA1-GTPase and comprehensively improve mitochondrial health to ameliorate cardiac hypertrophy. These findings underscore mitochondrial abnormality as a primary contributor to pathological cardiac remodeling and present OPA1 as a strong potential drug target. The underlying mechanism of this novel agonist DNJ5a may pave the way towards developing many other promising mitochondrial-targeted therapeutics.
    Keywords:  1-deoxynojirimycin; cardiomegaly; mitochondria; mitophagy; optic atrophy, autosomal dominant
    DOI:  https://doi.org/10.1161/CIRCRESAHA.125.327407
  35. Toxicol Lett. 2025 Dec 30. pii: S0378-4274(25)02760-2. [Epub ahead of print] 111814
       INTRODUCTION: While fine particulate matter (PM2.5) is an established risk factor for cardiovascular disease (CVD), the relative contribution of its specific chemical components to cardiotoxicity remains unclear. This study aimed to systematically compare the cytotoxicity driven by the oxidative potential (OP) of different PM2.5 components and elucidate the underlying mechanisms.
    METHODS: We conducted a comparative assessment of the water-soluble particle (WSP), non-water-soluble particle (NWSP), and organic matter (OM) of PM2.5 collected in winter in Taiyuan, China, in H9c2 cardiomyocytes, focusing on OP, cytotoxicity, and mitochondrial biogenesis. OP was measured by the dithiothreitol (DTT) assay, a non-cellular method. The mitochondrial biogenesis-related gene expressions (AMPKα, PGC-1α, Nrf1, Nrf2, TFAM) were quantified by RT-qPCR and western blot. The mitochondrial DNA (mtDNA) copy number was detected. The correlation between the PM2.5 composition (water-soluble ions, metals, and PAHs, etc.) and OP was analyzed.
    RESULTS: Among the three components, OM exhibited the highest OP values. Cellular experiments consistently demonstrated that the OM was the most potent inducer of ROS, LDH release, and ATP depletion, and displayed the lowest LD50. Mechanistically, it most severely suppressed mtDNA copy number and the expression of key regulators of mitochondrial biogenesis, including AMPKα, PGC-1α, and its downstream targets Nrf1, Nrf2, and TFAM. Critically, correlation analysis revealed that the OP was strongly associated with the content of PM2.5-bound PAHs.
    CONCLUSION: The OM fraction, particularly the PAHs, is the primary driver of PM2.5-induced cardiomyocyte toxicity. This effect is mediated through a mechanism involving high oxidative potential, which triggers severe oxidative stress and disrupts mitochondrial biogenesis. This study provides crucial experimental evidence for the increased CVD risk associated with PM2.5.
    Keywords:  H9c2 cell; Mitochondrial biogenesis; Organic matter; Oxidative potential; PM(2.5); cytotoxicity
    DOI:  https://doi.org/10.1016/j.toxlet.2025.111814
  36. Neurooncol Adv. 2025 Jan-Dec;7(1):7(1): vdaf228
       Abstract: BackgroundEmbryonal tumor with multilayered rosettes (ETMR) is an aggressive pediatric brain tumor that carries a poor prognosis, and there is currently no standard of care. Dysregulated mitochondrial bioenergetics and dynamics have been associated with the progression of diverse cancers. Cardiolipins are mitochondrial-specific lipids, and their fatty acid composition has been shown to regulate mitochondrial structure and function. Despite the known functional significance of cardiolipins, their structure-specific accumulation in relation to mitochondrial phenotypes in ETMR remains ill-defined.
    Methods: Spatial lipidomic profiles in patient samples and 3D models were determined using mass spectrometry imaging. Cell proliferation and mitochondrial bioenergetics and dynamics were characterized using immunohistochemistry, transmission electron microscopy, Western blotting, and metabolic assays. LCLAT1 KD was carried out using siRNA.
    Results: We detected a structure-specific accumulation of cardiolipins and increased expression of the cardiolipin acyl chain remodeling enzyme, lysocardiolipin acyltransferase 1 (LCLAT1), within proliferating tumor cells in patient samples and the 3D tumorspheres. Orthogonal imaging techniques correlated the structure-specific accumulation of cardiolipin with fragmented mitochondria displaying aberrant cristae structure, altered mitochondrial dynamics, decreased expression of respiratory chain enzymes, and a more glycolytic phenotype. LCLAT1 KD altered cardiolipin profiles, reduced growth and proliferation, decreased Sox2 and N-Myc expression, increased p53 and p21 expression, and increased LIN28A and Dcx expression. Additional therapeutic targeting of the fragmented mitochondrial phenotype identified also resulted in selective inhibition of ETMR growth and viability.
    Conclusions: Our findings provide novel insight into ETMR biology based on mitochondrial phenotypes and the fatty acid composition of the multifunctional mitochondrial-specific lipid, cardiolipin.
    Keywords:  ETMR; LCLAT1; cardiolipins; mitochondrial dynamics and bioenergetics; pediatric brain tumors
    DOI:  https://doi.org/10.1093/noajnl/vdaf228
  37. J Cell Mol Med. 2026 Jan;30(1): e70999
       RETRACTION: S.-H. Dai, Q.-C. Wu, R.-R. Zhu, X.-M. Wan and X.-L. Zhou, "Notch1 Protects Against Myocardial Ischaemia-Reperfusion Injury via Regulating Mitochondrial Fusion and Function," Journal of Cellular and Molecular Medicine 24, no. 5 (2020): 3183-3191, https://doi.org/10.1111/jcmm.14992. The above article, published online on 23 January 2020 in Wiley Online Library (wileyonlinelibrary.com), has been retracted by agreement between the authors; the journal Editor-in-Chief, Stefan N. Constantinescu; the Foundation for Cellular and Molecular Medicine; and John Wiley & Sons Ltd. The retraction has been agreed upon following concerns raised by a third party. An investigation determined that Figures 4C, 4D, and elements of Figure 6B, duplicate figures previously published in other articles by a different author group. Due to errors in image management leading to unreliable data, the authors have voluntarily requested retraction. The editors consider the results and conclusions compromised.
    DOI:  https://doi.org/10.1111/jcmm.70999
  38. Am J Pathol. 2025 Dec 30. pii: S0002-9440(25)00462-6. [Epub ahead of print]
      Ameloblastoma (AM), a locally aggressive odontogenic tumor, exhibits elusive pathogenesis. Here, we identify OPA1-mediated mitochondrial hyperfusion as a driver of tumor stemness and progression. Single-cell transcriptomics of primary AM specimens revealed mitochondrial fusionHigh epithelial subpopulations exhibiting enriched stemness pathways. We observed a striking upregulation of OPA1 in AM tissues, establishing a robust correlation between elevated OPA1 expression and upregulated stemness markers, while functional experiments demonstrated that OPA1 overexpression amplifies self-renewal capacity and invasive aggression in hTERT+-AM cells. Mechanistically, mitochondrial hyperfusion suppresses Hippo signaling, enabling YAP1 nuclear translocation and TEAD-dependent transcription. OPA1-overexpressing cells exhibited robust nuclear YAP1 enrichment, driving stem-like expansion. Critically, clinical analysis established OPA1High tumors as having elevated growth rates, consolidating mitochondrial hyperfusion as a prognostic determinant. Therapeutically, MYLS22-a first-in-class OPA1 inhibitor-suppressed mitochondrial hyperfusion and reduced stemness in patient-derived organoids. Our work unveils an OPA1-mediated mitochondrial fusion-YAP1 nuclear translocation axis as the cornerstone of AM stemness, proposing OAP1 as a druggable target for this recalcitrant tumor.
    Keywords:  Ameloblastoma; Mitochondrial fusion; Stemness; YAP1
    DOI:  https://doi.org/10.1016/j.ajpath.2025.12.002
  39. Cell Death Discov. 2025 Dec 29.
      Renal fibrosis is a major driver of chronic kidney disease (CKD) progression, yet targeted therapies remain limited due to incomplete understanding of key molecular mechanisms. While IL-1-mediated inflammation and mitochondrial dysfunction are recognized contributors, the precise links between IL-1 signaling, fibrosis, and mitochondrial homeostasis are unclear. Here, we investigated the therapeutic effects of recombinant human IL-1 receptor antagonist (rhIL-1Ra) in both acute (UUO) and chronic (5/6Nx) mouse models of kidney injury, as well as in vitro TGF-β1-stimulated kidney cells. rhIL-1Ra significantly attenuated renal fibrosis, inflammation, and functional impairment in vivo. Mechanistically, rhIL-1Ra suppressed TGF-β1-induced expression of the E3 ubiquitin ligase RNF182, which we show mediates MFN2 ubiquitination and degradation, leading to mitochondrial dysfunction. Inhibition of RNF182 by rhIL-1Ra stabilized MFN2, preserved mitochondrial respiration and ATP production, and reduced oxidative stress. Rescue experiments confirmed the centrality of the RNF182-MFN2 axis in fibrotic and mitochondrial injury. Our findings reveal a novel IL-1R/RNF182/MFN2 pathway linking inflammation to mitochondrial and fibrotic pathology, supporting RNF182 as a promising target and rhIL-1Ra as a potential therapy for CKD.
    DOI:  https://doi.org/10.1038/s41420-025-02929-4
  40. Cell Biosci. 2025 Dec 27.
      Peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) is a crucial coactivator that regulates mitochondrial biogenesis and function across diverse tissues, including the brain, heart, skeletal muscle, bone marrow, and liver. The diversity of PGC-1α isoforms in distinct tissues allows this co-transcription factor to exert wide-ranging biological effects, including regulating mitochondrial functions, oxidative stress, and endoplasmic reticulum homeostasis. Here, we focus on the key roles of PGC-1α in cell differentiation. Initially identified in brown adipose tissue in response to cold exposure, PGC-1α regulates cell differentiation by modulating gene expression networks involved in mitochondrial biogenesis. PGC-1α influences cell fate in several cell types, including adipocytes, skeletal muscle cells, and bone marrow-derived cells. A deeper understanding of PGC-1α provides valuable insights into developmental biology, tissue formation, and potential therapeutic targets for regenerative medicine and disease treatment. This review explores recent progress in understanding the roles of PGC-1α in cell differentiation, offering an integrated perspective on its significance in tissue and organism development.
    Keywords:  Cell differentiation; Metabolic reprogramming; PGC-1α; Tissue regeneration
    DOI:  https://doi.org/10.1186/s13578-025-01519-2
  41. Breast Cancer (Dove Med Press). 2025 ;17 1265-1278
       Research Purpose: To investigate how dexmedetomidine (DEX) controls the proliferation and death of breast cancer cells.
    Methods: Human breast cancer cells were cultured in vitro with DEX at different concentrations (25, 50, 100 ng/mL) or 30 μM LY294002. Cancer cell viability, proliferation, apoptosis and the expression of Microtubule-associated protein light chain 3 (LC3)-II/LC3-I protein were separately analyzed using cell counting kit 8 (CCK-8), colony formation, flow cytometry and Western blot assays after DEX treatment. The effect of DEX on mitochondrial membrane potential (MMP) level in cancer cells was determined using immunofluorescence. The expressions of B cell lymphoma-2 (Bcl-2), Bcl-2 associated X (Bax), phosphatidylinositol 3-kinase (PI3K), phosphorylated (p)-PI3K, protein kinase B (AKT) and p-AKT in DEX-treated cancer cells were measured by Western blot.
    Results: DEX promoted cell growth activity and proliferation, inhibited cell autophagy and apoptosis and down-regulated the ratio of LC3-II/LC3-I to reverse the effect of LY294002 on breast cancer cells. DEX also abrogated LY294002-induced down-regulation of MMP, p-PI3K/PI3K, p-AKT/AKT and Bcl-2 and up-regulation of Bax in breast cancer cells.
    Conclusion: DEX may promote the development of breast cancer cells while preventing cancer cell autophagy and apoptosis in vitro via PI3K/AKT signaling.
    Keywords:  PI3K/AKT signaling; apoptosis; breast cancer; dexmedetomidine; mitochondrial autophagy
    DOI:  https://doi.org/10.2147/BCTT.S543090
  42. Free Radic Biol Med. 2025 Dec 25. pii: S0891-5849(25)01458-3. [Epub ahead of print]
      Protein O-GlcNAcylation (O-GlcNAc) is a nutrient-responsive posttranslational modification (PTM). Proper regulation of brain O-GlcNAc levels is essential for the coupling between metabolic homeostasis and neuronal function. Abnormal O-GlcNAc levels in the brain are associated with neurodevelopmental and neurodegenerative diseases related to defects in energy metabolism. We investigated the levels and regulation of protein O-GlcNAc modification and related pathways through gene and protein expression analysis in the hippocampus of two well-established murine models of Rett syndrome (RTT), a monogenic neurodevelopmental disorder with metabolic components and a primary cause of severe intellectual disability in females. Increased protein O-GlcNAc levels, due to changes in the molecular machinery that controls O-GlcNAc production, transfer, and removal, were observed in the hippocampus of the two RTT mouse models (MeCP2-BIRD and MeCP2-308 models). Remarkably, systemic administration of the OGT inhibitor OSMI-1 restored O-GlcNAc brain homeostasis and rescued brain mitochondrial defects and redox alterations in the RTT mouse hippocampus. The OSMI-1 treatment also induced a normalization of the cognitive performance of RTT mice in novel object recognition tests and reduced peripheral oxidative stress. These findings provide new evidence of an imbalance in nutrient-sensing O-GlcNAc in the RTT mouse hippocampus, suggesting that restoring brain O-GlcNAc homeostasis might represent a promising therapeutic approach for RTT.
    Keywords:  O-GlcNAc; OGT/OGA; OSMI-1; Rett syndrome; mitochondrial homeostasis; mouse models
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2025.12.042
  43. J Immunother Cancer. 2025 Dec 30. pii: e011477. [Epub ahead of print]13(12):
       BACKGROUND: Mitochondrial antiviral signaling protein (MAVS), a central adaptor in cytosolic RNA sensing, is critical for antitumor innate immunity and maintains mitochondrial homeostasis via its mitochondrial localization. Mitochondrial dysfunction acts as a key driver and amplifier of the senescence-associated secretory phenotype (SASP), a double-edged sword in tumor progression. However, whether tumor-intrinsic MAVS can regulate antitumor immunity via cellular senescence independently of its well-established interferon signaling remains unclear.
    METHODS: Our study employed an integrated strategy. Clinically, we profiled MAVS expression and its association with prognosis and immune infiltration in renal tumor specimens. Mechanistic insights into tumor-intrinsic MAVS were gained through a battery of techniques spanning quantitative PCR, immunoblotting, RNA sequencing, senescence and mitochondrial function assays, confocal imaging, immunohistochemical, mass spectrometry, and co-immunoprecipitation. In vivo, we used MAVS-deficient models combined with CD8+ T-cell depletion, programmed cell death protein-1 (PD-1) blockade, or reactive oxygen species (ROS) scavenging by N-acetylcysteine (NAC), with immune infiltration characterized by flow cytometry.
    RESULTS: Clinical evidence links elevated MAVS expression in renal tumors to poor prognosis and diminished CD8+ T-cell infiltration. Strikingly, tumor-intrinsic MAVS deficiency curbed malignant progression by triggering cellular senescence and fostering a permissive niche for CD8+ T-cell activation and recruitment. Mechanistically, MAVS orchestrates mitochondrial integrity by co-localizing with and stabilizing chemokine-like factor-like MARVEL transmembrane domain-containing 6 (CMTM6), thereby shielding it from lysosomal degradation. Disruption of this axis provoked mitochondrial dysfunction and ROS accumulation, culminating in senescence and an SASP marked by chemokine C-C motif ligand 3 (CCL3). Thus, despite dampening canonical innate immune signaling, MAVS deletion unleashed potent antitumor immunity via CCL3-mediated CD8+ T-cell recruitment, an effect abolished by CD8+ T-cell depletion or ROS scavenging with NAC. Leveraging this paradigm, we demonstrated that tumor-specific MAVS deficiency acts synergistically with PD-1 blockade to achieve robust therapeutic efficacy.
    CONCLUSIONS: Our findings establish the tumor-intrinsic MAVS/CMTM6/CCL3 axis as a previously unrecognized critical regulator of senescence-driven antitumor immunity in renal carcinoma. Therapeutic targeting of this axis presents a promising strategy to curtail tumor progression and potentiate immunotherapy.
    Keywords:  Cytokine; Immune modulatory; Innate; Kidney Cancer; Tumor microenvironment - TME
    DOI:  https://doi.org/10.1136/jitc-2025-011477
  44. Cell Mol Immunol. 2026 Jan 01.
      Melanoma Differentiation-Associated gene 5 (MDA5) serves as a pattern recognition receptor (PRR) that identifies pathogen-associated molecular patterns (PAMPs), making it instrumental in antiviral defense. However, its non-canonical role in adaptive immunity, particularly in regulating B-cell immune functions, is poorly characterized. Here, we demonstrate that MDA5 is critical for the marginal zone (MZ) B-cell differentiation, B-cell receptor (BCR) signal transduction, and cytoskeletal dynamics. We determined that the MDA5-NF-κB-DNM1 axis governs actin polymerization and that this impairment in Mda5 knockout (KO) B cells can be rescued by the treatment with the dynamin1 (DNM1) activator Bis-T-23. Furthermore, MDA5 deficiency induces metabolic perturbations in B cells, characterized by a reduced extracellular acidification rate (ECAR) and oxygen consumption rate (OCR), excessive reactive oxygen species (ROS) accumulation, and increased mitochondrial fission. Notably, taurine levels are decreased in Mda5 KO B cells, and in vitro taurine supplementation rescues impaired BCR signaling. Finally, MDA5-deficient mice exhibit a blunted humoral immune response. Overall, this study reveals the key functions and molecular mechanisms of MDA5 in B-cell differentiation, BCR signaling, and the humoral immune response.
    Keywords:  B cells; BCR signal transduction; Cytoskeleton dynamics; DNM1; MDA5; Mitochondrial fission
    DOI:  https://doi.org/10.1038/s41423-025-01352-0
  45. Chemosphere. 2025 Dec 26. pii: S0045-6535(25)00755-6. [Epub ahead of print]394 144807
      Nano- and microparticles (NMPs) hold great promise for applications in medicine, industry, and agriculture, but concerns about their impact on human health persist due to their small size and unique properties. This study investigates the cytotoxic effects of three representative NMPs: titanium dioxide (TiO2), polystyrene (Psty), and a chitosan-based biopolymer (CSFe). Two of these (TiO2 and Psty) are known for potential toxicity, while CSFe is less studied. Here, we examined the impact of these particles on two critical regulators of cellular homeostasis: microtubules and mitochondria. Cell viability assays revealed that CSFe particles were the least harmful, whereas TiO2 and Psty particles, particularly the larger (0.5 μm) ones, which were significantly toxic. Interestingly, 0.2 μm Psty particles caused less toxicity than both smaller (0.1 μm) and larger Psty, likely due to lower cellular uptake. Further investigation showed that only CSFe and 0.2 μm Psty particles induced microtubule hyperacetylation, a stress response associated with cell survival. TiO2 damaged microtubule networks without inducing hyperacetylation but altered the distribution of the +TIP protein CLIP-170, indicating impaired microtubule function and more particularly in growth rate capacity. Mitochondrial analysis revealed that CSFe did not affect mitochondrial morphology, while Psty (0.1 and 0.5 μm) caused fragmentation, a sign of cellular stress. TiO2 had a milder impact. Overall, the study highlights the importance of particle size and composition in determining cellular impact and underscores the relevance of microtubules and mitochondrial alterations as markers of NMP toxicity.
    DOI:  https://doi.org/10.1016/j.chemosphere.2025.144807