bims-mikwok Biomed News
on Mitochondrial quality control
Issue of 2026–02–22
48 papers selected by
Gavin McStay, Liverpool John Moores University



  1. Adv Sci (Weinh). 2026 Feb 17. e19792
      Metastatic invasiveness emerges from coordinated intrinsic programs and microenvironmental cues that converge on mitochondrial quality control (MQC). Here, we use "context" to denote stage- and site-aware constellations of tumor-intrinsic states (e.g., mtROS tone, mtDNA integrity, epigenetic wiring, cellular stiffness, oncogenic mutations) and extrinsic landscapes (oxygen-nutrient availability, ECM mechanics, stromal/inflammatory signals). These axes jointly shape mitochondrial adaptation by tuning bioenergetics, redox balance, metabolic plasticity, fission-fusion dynamics, mechanosensitive hubs, and Ca2 + homeostasis. As pressures intensify, mitochondrial vulnerabilities-such as mtDNA compromise and mtUPR activation-signal the engagement of mitophagy to preserve organelle fitness under stress. Through these coupled changes in mitochondrial performance and stress responses, context governs EMT/MET plasticity and transitions across migratory, invasive, and proliferative states. Mechanistically, ubiquitin conjugation, via E3 ligases and deubiquitinases, serves as an integrating conduit that links mitochondrial remodeling and mitophagy to cytoskeletal reprogramming and invasive behavior. This ubiquitin-mitochondria interface therefore represents a coherent therapeutic entry point; translational strategies including PROTAC-enabled targeting and selective E3/DUB or mitophagy-pathway modulators may rebalance pathological ubiquitin signaling, restore mitochondrial homeostasis, and constrain tumor dissemination.
    Keywords:  EMT–MET plasticity; extracellular matrix mechanics; hypoxia and nutrient deprivation; mitochondrial ROS; mitochondrial dynamics; mitophagy; ubiquitination
    DOI:  https://doi.org/10.1002/advs.202519792
  2. Front Mol Biosci. 2026 ;13 1778855
       Purpose: Acute kidney injury (AKI) remains a global health concern with limited therapies. Among its causes, arsenic (AS)-induced AKI (AI-AKI), exemplified by the antitumor agent arsenic trioxide (ATO), represents an emerging clinical challenge. Despite its clinical efficacy in treating AI-AKI, the protective mechanism of Chuanhuang Fang III (CHF) remains unclear. This study aimed to investigate the mechanisms and therapeutic targets of CHF against AI-AKI.
    Methods: Classic AI-AKI rat model was established, and subsequently treated with graded doses of CHF. CHF constituents were identified. Renal pathology, renal function, and AKI biomarkers were detected. Mitochondrial quality control-related parameters were detected as follows: 1) transmission electron microscopy was employed to assess mitophagy; 2) Western blotting was performed to evaluate mitochondrial dynamics- and mitophagy-related proteins, while differential gene expression and pathway enrichment were analyzed by RNA-sequencing; 3) mitochondrial membrane potential and mitochondrial ROS levels were measured in freshly isolated renal cortical mitochondria by JC-1 staining and flow cytometry. The HK-2 cell line was used to further elucidate the underlying mechanisms of AI-AKI, and the effect of antioxidant NAC was observed simultaneously.
    Results: ATO exposure resulted in increased serum creatinine, mitochondrial dysfunction, elevated mitochondrial ROS levels, and promoted apoptosis, autophagy, and mitophagy in renal tubular epithelial cells. It also downregulated the mitochondrial fusion protein OPA1 and upregulated the fission protein Drp1. These effects correlated with the activation of the PINK1/Parkin mitophagy pathway, as well as increased expression of BNIP3, NIX, LC3B and Bax, and decreased anti-apoptotic protein Bcl-2. Transcriptomic analysis indicated that the key signaling pathways in AI-AKI were associated with mitophagy, autophagy, mitochondrial function and apoptosis. CHF attenuated AI-AKI by regulating OPA1/Drp1 balance and PINK1/Parkin-mediated mitophagy and counteracted the associated pathological processes. In vitro experiments using the HK-2 cell line provided further evidence supporting the in vivo findings.
    Conclusion: The pathogenesis of clinical-dose ATO-induced AKI involves OPA1- and Drp1-mediated mitochondrial dynamics imbalance and PINK1/Parkin-dependent mitophagy in renal tubular epithelial cells, CHF ameliorated this injury by restoring mitochondrial quality control, highlighting its therapeutic potential against AI-AKI.
    Keywords:  Chuanhuang Fang III; acute kidney injury; arsenic trioxide; mitochondrial quality control; mitochondrialdynamics; mitophagy
    DOI:  https://doi.org/10.3389/fmolb.2026.1778855
  3. Autophagy. 2026 Feb 19. 1-2
      BNIP3L/NIX is a mitophagy receptor highly expressed in the brain. Unlike most mitophagy receptors that are recruited to mitochondria only upon stress, BNIP3L constitutively localizes to the mitochondrial outer membrane, suggesting functions beyond stress-induced mitophagy. Here, we identify a non-mitophagic role of BNIP3L in neuronal physiology. Conditional deletion of Bnip3l in glutamatergic neurons of the basolateral amygdala selectively impairs contextual fear memory in mice, a phenotype rescued by both wild-type BNIP3L and a mitophagy-deficient BNIP3L mutant lacking the LC3-interacting region motif. Mechanistically, BNIP3L competitively binds AMP-activated protein kinase (AMPK), thereby relieving AMPK-dependent inhibitory phosphorylation of DNM1L/DRP1 (dynamin 1 like) at Ser637. This interaction promotes rapid mitochondrial fission, supporting synaptic energy availability during memory encoding. Together, these findings reveal a switchable function of BNIP3L in neurons, acting either to acutely regulate mitochondrial dynamics to meet energetic demand or to engage mitophagy when mitochondrial function becomes compromised.
    Keywords:  BNIP3L/NIX; Basolateral amygdala; fear memory; mitochondrial dynamics; mitophagy
    DOI:  https://doi.org/10.1080/15548627.2026.2634183
  4. Free Radic Biol Med. 2026 Feb 13. pii: S0891-5849(26)00125-5. [Epub ahead of print]
      Di(2-ethylhexyl) phthalate (DEHP) is a widely used plasticizer known to cause testicular toxicity, though its mechanism remains incompletely understood. This study investigated whether DEHP-induced testicular injury involved suppression of androgen receptor (AR) expression. In vivo, rats were exposed to DEHP (500 mg/kg) for 60 days, causing damage to the testicles. Further, the expression of AR was decreased, mitochondrial quality control (MQC) was impaired, mitochondrial damage occured, and ultimately led to ferroptosis. Specifically, DEHP reduced levels of mitochondrial biogenesis markers (PGC-1α, TFAM, NRF1/2) and fusion markers (MFN1/2, OPA1), while increasing fission markers (DRP1, FIS1) and mitophagy markers (PINK1, PARKIN). In vitro, to further explore the relationship between AR, MQC, and ferroptosis, the TM4 cell model overexpressing AR was established and exposed to MEHP (200 μM). The findings demonstrated that AR overexpression effectively alleviated DEHP-induced disruption of MQC, mitochondrial impairment, and ferroptosis. Together, these findings demonstrated that DEHP impaired the MQC system by inhibiting AR expression, thereby promoting ferroptosis.
    Keywords:  Androgen receptor; DEHP; Ferroptosis; Mitochondrial quality control; Testicular injury
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.02.028
  5. Aging Cell. 2026 Feb;25(2): e70416
      Age-related macular degeneration (AMD) stands as a leading cause of blindness in the elderly, yet the fundamental aging processes that underpin its pathogenesis remain incompletely defined. The dysfunction of retinal pigment epithelial (RPE) cells is a central event in AMD, a process that shares key hallmarks with broader cellular aging, particularly the progressive decline in mitochondrial function. In this study, we investigated how a common environmental stressor-blue light-triggers a key pathological transformation, epithelial-mesenchymal transition (EMT), in RPE cells by specifically disrupting mitochondrial dynamics, a core pillar of cellular aging. Using an in vitro model of human RPE cells, we demonstrated that blue light exposure induces a marked shift in mitochondrial dynamics towards excessive fission. This imbalance directly resulted in mitochondrial dysfunction, elevated oxidative stress, and served as the critical driver for the initiation of EMT. Importantly, pharmacological inhibition of the mitochondrial fission GTPase Dynamin-related protein 1 (Drp1) with Mdivi-1 effectively restored mitochondrial network homeostasis, rescued mitochondrial function, and fully reversed the EMT phenotype. These findings were corroborated in a mouse model of blue light-induced retinal damage, where Drp1 inhibition successfully preserved retinal light responses, mitigated structural degeneration, and slowed disease progression. Our study demonstrates that Drp1-mediated excessive mitochondrial fission drives EMT in RPE cells under blue light, linking this mechanism to AMD progression. Consequently, targeting mitochondrial dynamics to maintain cellular homeostasis emerges as a promising and broadly applicable geroscience-based strategy for mitigating age-related tissue dysfunction.
    Keywords:  Drp1; age‐related macular degeneration; epithelial‐mesenchymal transition; mitochondrial dynamics; oxidative stress; retinal pigment epithelial
    DOI:  https://doi.org/10.1111/acel.70416
  6. PeerJ. 2026 ;14 e20700
      Mitophagy is a pivotal quality control pathway that maintains cardiac energy metabolism and structural stability by selectively removing damaged or senescent mitochondria, thereby keeping mitochondrial dynamics in balance. This process secures cardiomyocyte survival, calcium handling, and contractile function during both rest and stress. When mitophagic flux is inadequate, accumulation of reactive oxygen species, disruption of calcium homeostasis, and uncontrolled inflammation act together to drive pathological hypertrophy, heart failure, cardiac aging, and obesity-associated cardiomyopathy. Conversely, appropriate activation of mitophagy can lessen structural injury and restore pump performance during ischemia reperfusion, pressure overload, and metabolic stress. This review summarizes the central regulatory network of cardiac mitophagy and its pathological roles across cardiovascular disorders, emphasizing that careful modulation of flux is essential for preserving myocardial homeostasis. Recent experimental strategies that target mitophagy are also discussed, providing a theoretical foundation for the development of precise cardioprotective therapies.
    Keywords:  Cardiac aging; Cardiac hypertrophy and heart failure; Cardiomyocyte; Mitophagy
    DOI:  https://doi.org/10.7717/peerj.20700
  7. Tissue Cell. 2026 Feb 15. pii: S0040-8166(26)00084-4. [Epub ahead of print]100 103392
      Acute lung injury (ALI) is a critically ill condition with extremely high mortality rates, where mitophagy dysfunction exacerbates inflammatory responses. Mammalian STE20-like kinase 1 (MST1), a serine/threonine kinase involved in mitochondrial regulation, has been identified as a potential regulator of inflammatory diseases. This study aims to investigate the role of MST1 in mitochondrial function and mitophagy using an LPS-induced ALI model. MST1 was overexpressed or silenced by siRNA in LPS-stimulated cells via lentiviral transfection. Mitochondrial function was assessed using JC-1 staining, mitochondrial permeability transition pore (mPTP) opening detection, and reactive oxygen species (ROS) detection. Protein expression was analyzed by Western blot. The JNK/p53/BNIP3 pathway was examined using Western blot, qRT-PCR, immunofluorescence, and interventions with siRNA-p53 and the JNK inhibitor SP600125. MST1 overexpression exacerbated mitochondrial dysfunction, manifested as reduced membrane potential, increased mPTP opening, and ROS levels. Concurrently, it suppressed mitophagy by downregulating key mitophagy-related proteins and enhanced proinflammatory cytokine expression. Silencing MST1 produced opposite effects. Mechanistically, MST1 activates the JNK/p53 pathway, thereby inhibiting the mitophagy receptor BNIP3. In summary, MST1 suppresses BNIP3 via the JNK/p53 pathway, thereby promoting inflammation and impairing mitophagy in LPS-induced injury. These findings not only identify MST1 as a potential therapeutic target for ALI but also elucidate a novel mechanism regulating mitochondrial homeostasis during inflammation.
    Keywords:  Acute lung injury; BNIP3; JNK/p53 signaling pathway; MST1; Mitophagy
    DOI:  https://doi.org/10.1016/j.tice.2026.103392
  8. Biotechnol J. 2026 Feb;21(2): e70196
       BACKGROUND: Osteoarthritis (OA) is a progressive degenerative disorder driven by complex pathogenic mechanisms. Increasing evidence indicates that NLRP3 inflammasome-mediated chondrocyte pyroptosis contributes critically to OA progression. Cellular repressor of E1A-stimulated gene 1 (CREG1), a secreted glycoprotein involved in cellular homeostasis and lysosomal function, has not been well characterized in OA. This study aimed to investigate the role of CREG1 in OA and its underlying molecular mechanisms.
    METHODS: Human knee OA cartilage samples were analyzed to evaluate the association between CREG1 expression and chondrocyte pyroptosis. An LPS/ATP-induced in vitro pyroptosis model was used to assess the effects of CREG1 on chondrocyte apoptosis, extracellular matrix (ECM) degradation, NLRP3 inflammasome activation, and PINK1/Parkin-dependent mitophagy. Cyclosporin A (CsA) was applied to inhibit mitophagy.
    RESULTS: CREG1 expression was significantly reduced in OA cartilage and negatively correlated with chondrocyte pyroptosis. CREG1 silencing aggravated apoptosis and ECM degradation, promoted NLRP3 inflammasome activation, impaired mitophagy, and disrupted mitochondrial function. Conversely, CREG1 overexpression restored PINK1/Parkin-mediated mitophagy, improved mitochondrial homeostasis, and suppressed NLRP3 inflammasome activation. These effects were abolished by CsA treatment.
    CONCLUSIONS: CREG1 protects against OA progression by suppressing NLRP3 inflammasome-driven chondrocyte pyroptosis through activation of PINK1/Parkin-dependent mitophagy, highlighting CREG1 as a potential therapeutic target.
    Keywords:  CREG1; NLRP3 inflammasome; mitophagy; osteoarthritis; pyroptosis
    DOI:  https://doi.org/10.1002/biot.70196
  9. Autophagy Rep. 2026 ;5(1): 2627062
      In PINK1 (PTEN induced kinase 1)/PRKN (Parkin)-mediated mitophagy, the rupture of the outer mitochondrial membrane (OMM) emerges as a crucial event required for efficient mitochondrial clearance. Mechanistically, OMM rupture exposes inner mitochondrial membrane (IMM) mitophagy receptors, facilitating subsequent autophagic removal. Despite the important role of OMM rupture in mitophagy, the underlying mechanism remains elusive and technically difficult to monitor. In a recent study, we developed a novel fluorescent biosensor to directly visualize OMM rupture. This technique enables temporal and spatial characterization of OMM rupture and provides a powerful platform to dissect the underlying mechanism. Using this tool, we revealed that VCP (valosin containing protein) and its recruitment factors are required for OMM rupture, suggesting that VCP-dependent remodeling of the OMM proteome primes the rupture of OMM during mitophagy. Abbreviations: ARIH1, Ariadne RBR E3 ubiquitin protein Ligase 1; AMFR, autocrine motility factor receptor; ANKRD13A, ankyrin repeat domain-containing protein 13 A; FUNDC1, FUN14 domain containing 1; OA, oligomycin and antimycin; CID, chemical-induced dimerization; IMM, nner mitochondrial membrane; LC3, microtubule-associated protein 1 light chain 3; MUL1, mitochondrial E3 ubiquitin protein ligase 1; NIX, BCL2 interacting protein 3 like; OMM, outer mitochondrial membrane; UBXN1, ubiquitin regulatory X domain-containing protein 1; UBXN6, ubiquitin regulatory X domain-containing protein 6; VCP, valosin-containing protein; WIPI2, WD repeat domain phosphoinositide interacting protein 2.
    Keywords:  Biosensor; Mitochondrial outer membrane rupture; Mitochondrial quality control; PINK1/Parkin-mediated mitophagy; VCP
    DOI:  https://doi.org/10.1080/27694127.2026.2627062
  10. J Mol Histol. 2026 Feb 16. 57(2): 79
      Cervical cancer is the fourth most common cancer in women worldwide. Mitochondrial E3 ubiquitin ligase 1 (MUL1) plays a crucial role in cancer processes, yet its role in cervical cancer remains unclear. Here, we observed that MUL1 mRNA and protein levels were reduced in cervical cancer tissues and cells using qRT-PCR and Western blot assays. Patients with low MUL1 expression exhibited poor survival. CCK-8, EdU, Transwell and flow cytometry analysis demonstrated that MUL1 overexpression inhibited cervical cancer cell proliferation and migration and promoted cell apoptosis, while MUL1 knockdown had opposite effects. Interestingly, inhibition of mitophagy induced by Midivi-1 attenuated the effects of MUL1 knockdown on cell proliferation, migration, and apoptosis. Mechanistically, co-immunoprecipitation and ubiquitination assays demonstrated that MUL1 decreased FUN14 domain containing 1 (FUNDC1) protein stability by promoting its ubiquitination. FUNDC1 overexpression promoted dynamin-related protein 1 (DRP1) expression and promoted mitophagy in cervical cancer cells, whereas DRP1 knockdown reversed these changes. Notably, FUNDC1 knockdown weakened the promoting effects of MUL1 knockdown on mitophagy. FUNDC1 overexpression rescued the inhibitory effects on proliferation, migratory capacity and the promoting effect on apoptosis. In vivo, MUL1 overexpression inhibited tumor growth in a xenograft mouse model. These findings suggested MUL1 suppressed cervical cancer progression by targeting the FUNDC1/DRP1 axis and inhibiting mitophagy, highlighting its potential as a therapeutic target.
    Keywords:  Cervical cancer; DRP1; FUNDC1; MUL 1; Mitophagy; Ubiquitination
    DOI:  https://doi.org/10.1007/s10735-026-10745-y
  11. Mol Neurobiol. 2026 Feb 18. 63(1): 454
      Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized primarily by deterioration in memory, cognition, and learning ability. Its etiology is complex and influenced by multiple factors, including genetics and environment. With advancing research into mitochondrial function and mechanisms, impaired mitophagy has been proposed as a significant mechanism contributing to AD. The ApoE ε4 allele, a high-risk genetic factor for AD, may play a key role in disease pathogenesis by inducing mitophagy dysfunction and apoptosis. From the perspective of APOE gene polymorphisms, this study investigates abnormal changes in mitochondrial function and autophagy in humanized APOE4 mice primary astrocytes under oxidative stress, as well as the regulatory effect of curcumin (Cur) on mitophagy and oxidative stress-induced apoptosis, thereby exploring its potential to ameliorate AD through targeting mitophagy. Mitochondrial function analysis revealed that APOE4 expression reduced the antioxidant capacity and respiratory function of primary astrocytes, leading to mitochondrial membrane damage, intracellular reactive oxygen species (ROS) accumulation, and decreased ATP production. Curcumin effectively protected mitochondrial integrity, reduced the number of damaged mitochondria, improved overall mitochondrial function, and helped maintain mitochondrial homeostasis involving in PINK1/Parkin pathway. Regarding autophagy and apoptosis, curcumin was shown to restore autophagic flux, mitigate autophagy disruption caused by oxidative stress, and reverse early-stage apoptosis.
    Keywords:  APOE4; Astrocytes; Curcumin; Mitochondrial function; Mitophagy; Oxidative stress
    DOI:  https://doi.org/10.1007/s12035-026-05744-9
  12. STAR Protoc. 2026 Feb 16. pii: S2666-1667(26)00023-7. [Epub ahead of print]7(1): 104370
      Mitochondrial dynamics are essential for cellular homeostasis and can be visualized in adult Drosophila oenocytes using live-cell confocal imaging. Here, we present a protocol for live-cell imaging of mitochondrial dynamics in adult Drosophila oenocytes. We describe steps for fly preparation, dissection of abdominal cuticle to expose oenocytes, and mounting. We then detail procedures for time-lapse acquisition of mitochondria labeled with mitoGFP. Optimized imaging parameters enable reproducible visualization of mitochondrial morphology stably for longer durations.
    Keywords:  Cell Biology; Genetics; Microscopy; Model Organisms
    DOI:  https://doi.org/10.1016/j.xpro.2026.104370
  13. Parkinsonism Relat Disord. 2026 Feb 12. pii: S1353-8020(26)00054-4. [Epub ahead of print]145 108228
       BACKGROUND: Spinocerebellar ataxia type 12 (SCA12) is a late-onset, autosomal dominant neurodegenerative disorder linked to a CAG repeat expansion mutation in the PPP2R2B gene and prevalent in Indian Agarwal ancestry. The pathophysiology of SCA12 and its clinical relevance need further elucidation. Dysregulation of mitochondrial quality control (mitochondrial QC), a critical determinant of neurodegeneration, could play a central role in SCA12 pathogenesis.
    OBJECTIVES: In this study, 20 candidate genes regulating mitochondrial biogenesis, dynamics, mitophagy, mitochondrial transport, and protein folding were studied for their expression in SCA12 patient-derived peripheral blood mononuclear cells (PBMCs).
    METHODS: Twenty-four genetically confirmed SCA12 patients and healthy controls were recruited in the study. The patients were assessed for motor severity using the International Cooperative Ataxia Rating Scale (ICARS). PBMCs were isolated from the peripheral blood. Total RNA was extracted from the PBMCs, which were reverse transcribed to make cDNA. The relative mRNA expression was estimated using quantitative Real-time PCR.
    RESULTS: Among the 20 candidate genes, a total of 5 genes, i.e., DNM1L, PPARGC1A, OPA1, NFE2L2, and BECN1, demonstrated a significantly reduced expression in SCA12 compared to healthy controls. There was no difference in the expression of other genes between groups.
    CONCLUSION: This study suggests dysregulation of mitochondrial biogenesis, mitophagy, dynamics, and antioxidant system converging towards a compromised mitochondrial QC system in SCA12 patients.
    Keywords:  Gene expression; Mitochondrial quality control; Pathophysiology; Peripheral blood mononuclear cells; SCA12
    DOI:  https://doi.org/10.1016/j.parkreldis.2026.108228
  14. Neurol Res Int. 2026 ;2026 9860283
      [This retracts the article DOI: 10.1155/2015/742059.].
    DOI:  https://doi.org/10.1155/nri/9860283
  15. J Biochem Mol Toxicol. 2026 Mar;40(3): e70747
      Cadmium (Cd) is a common environmental contaminant that poses significant concern due to its neurotoxic effects. Mitophagy and apoptosis are two critical processes involved in Cd-induced central nervous system disorders, but the molecular mechanisms remain inadequately understood. Bcl2/adenovirus E1B 19 kDa protein-interacting protein 3-like (BNIP3L) is a crucial receptor protein that facilitates mitophagy. The study aimed to determine the precise mechanisms by which BNIP3L protects against Cd-induced neurotoxicity in the rat cerebral cortex. Following BNIP3L knockdown in the cerebral cortices, 24 male Sprague-Dawley rats were exposed to 50 mg/L Cd for 90 days. Histological alterations in the cerebral cortex were assessed using Nissl staining and transmission electron microscopy. Mitophagy- and apoptosis-related biomarkers were assessed using western blot analysis, immunofluorescence staining, and TUNEL staining. Our results revealed that BNIP3L knockdown increased COX IV expression, abolished the co-localization of LC3 and TOMM20, inhibited mitophagosome formation, and exacerbated Cd-induced cerebral cortex damage in rats. Moreover, BNIP3L knockdown exacerbated Cd-induced apoptosis and upregulated the Bax/Bcl-2 ratio, as well as the expression of cleaved caspase-9 and cleaved caspase-3. Collectively, our findings demonstrate that BNIP3L-mediated mitophagy provides neuroprotection in the rat cerebral cortex by inhibiting mitochondrial pathway-mediated apoptosis. Targeting mitophagy may have therapeutic promise for Cd-induced neurotoxicity.
    Keywords:  BNIP3L; apoptosis; cadmium; cerebral cortex; mitophagy
    DOI:  https://doi.org/10.1002/jbt.70747
  16. Free Radic Biol Med. 2026 Feb 16. pii: S0891-5849(26)00121-8. [Epub ahead of print]248 29-42
      PINK1 and Parkin are central regulators of mitophagy, a quality-control process essential for mitochondrial homeostasis and implicated in aging. However, their specific roles in ovarian physiology remain unclear. Here, we show that Pink1 deletion in mice leads to decreased ovarian weight, diminished ovarian reserve, and reduced oocyte quality, accompanied by increased granulosa cell apoptosis, accelerated ovarian ageing, and impaired fertility. Pink1 deficiency also compromises ovulation efficiency, increases oocyte cytoplasmic fragmentation, and disrupts meiotic spindle assembly, resulting in markedly reduced developmental competence of early embryos. Mechanistically, bulk and single-cell RNA sequencing reveal that loss of PINK1 impairs mitophagy and promotes transcriptional signatures of ovarian aging. In contrast, Parkin deletion exerts minimal effects on mitophagy, mitochondrial function, or ovarian physiology. Together, these findings identify PINK1, but not Parkin, as a critical regulator of ovarian aging through modulation of mitophagy.
    Keywords:  Mitophagy; Oocytes; Ovarian aging; PINK1; Parkin
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.02.024
  17. J Ethnopharmacol. 2026 Feb 15. pii: S0378-8741(26)00239-4. [Epub ahead of print]362 121388
       ETHNOPHARMACOLOGICAL RELEVANCE: Zhi-Zi-Hou-Po decoction, a classic herbal formula in traditional Chinese medicine, has long been used clinically for the treatment of depression. However, the precise molecular mechanisms underlying its antidepressant effects remain to be fully elucidated.
    AIM OF THE STUDY: This study aimed to characterize the chemical composition of ZZHP and investigate its antidepressant-like effects and underlying mechanisms, specifically focusing on the regulation of Mitochondrial Transcription Factor A (TFAM)-mediated mitophagy and the cGAS-STING innate immune pathway.
    MATERIALS AND METHODS: Chemical constituents of ZZHP were profiled using UPLC-Q-TOF-MS/MS. The antidepressant efficacy was evaluated in vivo using a Chronic Unpredictable Mild Stress (CUMS) mouse model with behavioral batteries (SPT, TST, FST, OFT) and in vitro using corticosterone (CORT)-injured PC12 cells. Mechanistic explorations involved immunofluorescence, Western blotting, transmission electron microscopy, and co-immunoprecipitation to assess mitochondrial integrity, autophagy flux, and the TFAM-LC3B interaction. Furthermore, TFAM-targeted siRNA transfection and a neuron-microglia co-culture system were employed to verify the molecular targets and intercellular crosstalk.
    RESULTS: Chromatographic analysis identified 22 bioactive compounds within ZZHP. In CUMS mice, ZZHP administration robustly ameliorated depressive-like behaviors, restored hippocampal neuronal morphology, and attenuated oxidative stress and neuroinflammation. Mechanistically, ZZHP upregulated neuronal TFAM expression and enhanced the formation of the TFAM-LC3B complex, thereby facilitating the autophagic clearance of damaged mitochondria and cytosolic mtDNA. This restoration of selective mitophagy effectively abrogated the activation of the cGAS-STING signaling pathway. Notably, TFAM knockdown in PC12 cells abolished the neuroprotective and anti-inflammatory effects of ZZHP, confirming TFAM as a critical therapeutic target. Additionally, ZZHP-conditioned neuronal medium promoted the polarization of microglia toward the anti-inflammatory M2 phenotype.
    CONCLUSION: These findings indicate that ZZHP exerts potent antidepressant effects by orchestrating TFAM-dependent mitophagy to eliminate immunogenic mtDNA, thereby inhibiting the cGAS-STING inflammatory axis and remodeling the neuroimmune microenvironment.
    Keywords:  Depressive-like behaviors; Mitophagy; TFAM; Zhi-Zi-Hou-Po decoction
    DOI:  https://doi.org/10.1016/j.jep.2026.121388
  18. Phytomedicine. 2026 Feb 16. pii: S0944-7113(26)00222-9. [Epub ahead of print]153 157985
       BACKGROUND: Secondary inflammatory cascades after spinal cord injury (SCI) drive progressive neurological deterioration, with microglial activation as a key determinant of lesion progression. Kakkalide, a naturally occurring isoflavone, exhibits antioxidant and anti-inflammatory activities; however, its efficacy and mechanism of action in SCI remain insufficiently defined.
    PURPOSE: To evaluate the therapeutic effects of kakkalide in SCI and delineate the molecular pathway through which it modulates microglia-driven neuroinflammation and functional recovery.
    METHODS: SCI was induced in mice to assess the effects of kakkalide on locomotor function and secondary inflammation. In vitro, LPS-stimulated BV2 microglia were used to examine phenotypic polarization. Proteomic profiling and molecular docking were performed to identify candidate targets of kakkalide. Mechanistic dependence was tested using the SIRT3-selective inhibitor 3-TYP in both cell and animal models. Immunofluorescence, western blotting, qPCR, and assays of mitochondrial membrane potential and mitochondrial reactive oxygen species (mtROS) were used to interrogate microglial phenotypes, mitochondrial homeostasis, and related signaling pathways.
    RESULTS: Kakkalide treatment significantly reduced secondary inflammation and improved locomotor recovery in SCI mice. In BV2 microglia, kakkalide promoted a shift from a pro-inflammatory M1-like state toward an anti-inflammatory M2-like phenotype. Mechanistically, kakkalide restored mitochondrial homeostasis by activating BNIP3/NIX-dependent mitophagy, thereby suppressing mtROS accumulation. Proteomics and docking analyses identified sirtuin 3 (SIRT3) as a putative direct target of kakkalide. Consistently, kakkalide increased SIRT3 expression and activity in microglia, and SIRT3 activity was required for kakkalide-induced mitophagy. Notably, co-administration of 3-TYP abrogated the neuroprotective and functional benefits of kakkalide in vivo.
    CONCLUSION: Kakkalide mitigates SCI by directly engaging SIRT3 and activating BNIP3/NIX-mediated mitophagy, which stabilizes mitochondrial function, limits oxidative stress, and biases microglia toward an M2-like protective phenotype. These findings define a previously unrecognized mechanism for kakkalide in SCI and nominate the SIRT3-mitophagy axis as a tractable therapeutic target for neuroinflammatory disorders.
    Keywords:  Kakkalide; Microglia; Mitochondria; SIRT3; Spinal cord injury
    DOI:  https://doi.org/10.1016/j.phymed.2026.157985
  19. Cell Rep. 2026 Feb 18. pii: S2211-1247(26)00056-2. [Epub ahead of print]45(3): 116978
      Hematopoietic stem and progenitor cells (HSPCs) arise from hemogenic endothelium via the endothelial-to-hematopoietic transition (EHT), a process requiring precise mitochondrial quality control. Here, we identify Clec16a, an E3 ubiquitin ligase, as a conserved regulator of embryonic HSPC emergence. In zebrafish and HEK293T models, Clec16a is enriched in hemogenic endothelium, and its loss disrupts arterial identity, impairs EHT, and reduces lymphoid, erythroid, and myeloid lineages. Transcriptomic and proteomic analyses show that Clec16a deficiency compromises mitophagy by promoting aberrant K48-linked ubiquitination and proteasomal degradation of ATG5, leading to mitochondrial dysfunction and elevated reactive oxygen species. These findings establish Clec16a as an essential regulator linking ubiquitin signaling, mitophagy, and hematopoietic fate specification. Our study defines a mitophagy-dependent checkpoint that safeguards mitochondrial homeostasis during developmental hematopoiesis and provides insight into the metabolic control of hematopoietic disorders.
    Keywords:  Atg5; CP: metabolism; CP: stem cell research; Clec16a; USP8; hematopoietic stem and progenitor cell; mitophagy; non-degradative ubiquitination; zebrafish
    DOI:  https://doi.org/10.1016/j.celrep.2026.116978
  20. Apoptosis. 2026 Feb 20. pii: 73. [Epub ahead of print]31(3):
      Cerebral ischemia/reperfusion injury (CI/RI) is a common complication of cerebrovascular diseases such as stroke, characterized by mitochondrial dysfunction. This study investigates the function of proliferation-associated protein 2G4 (PA2G4) released by neural stem cells (NSCs)-derived exosomes (NSC-Exo) in treating middle cerebral artery occlusion/reperfusion (MCAO/R) by regulating mitophagy. NSC-Exo were extracted and identified. Treatment of NSC-Exo alleviated neurofunctional impairments in MCAO/R-induced mice, reduced oxidative stress and inflammatory responses in hippocampal tissues, and decreased neuronal apoptosis. We analyzed the alteration of molecular mechanisms under the effect of NSC-Exo treatment using bioinformatics analysis and RNA sequencing. PA2G4 was enriched in NSC-Exo, and the absence of PA2G4 in neurons impaired the mitigating effect of NSC-Exo on hippocampal neuronal injury and inhibited mitophagy. NSC-Exo delivered PA2G4 to recruit WW domain-containing protein 2 (WWP2), thereby mediating ubiquitination and degradation of Annexin A2 (ANXA2), and overexpression of PA2G4 or WWP2 reversed the accentuating effect of ANXA2 overexpression on MCAO injury. These findings indicate that PA2G4 delivered by NSC-Exo recruits WWP2 to mediate ubiquitination of ANXA2, thereby activating mitophagy to alleviate oxidative stress in hippocampal neurons in MCAO/R. This study offers a novel target for the treatment of CI/RI.
    Keywords:  Cerebral ischemia/reperfusion injury; Mitophagy; Neural stem cells-derived exosomes; Oxidative stress; PA2G4
    DOI:  https://doi.org/10.1007/s10495-026-02291-5
  21. Stem Cells Dev. 2026 Feb 16. 15473287261423853
      Platelet biogenesis begins with the differentiation of hematopoietic stem cells (HSCs) into megakaryocytes (MKs) in the bone marrow, where mature MKs undergo endomitosis and ultimately release platelets. This program is tightly regulated by thrombopoietin, transcription factors, and metabolic cues, including mitochondrial reactive oxygen species and mitochondrial dynamics, which are now recognized as key drivers of megakaryopoiesis and thrombopoiesis. Sialic acid-binding immunoglobulin-like lectin (Siglec-7), a glycan-recognizing receptor, has been linked to mitochondrial dysfunction in natural killer cells, suggesting a potential role in modulating effector functions through oxidative phosphorylation. Here, using a phorbol 12-myristate 13-acetate (PMA)-induced K562 MK differentiation model, we examined how Siglec-7 expression relates to mitochondrial dynamics. Western blotting showed that mitochondrial dynamics-related proteins were markedly altered during PMA-induced differentiation, and confocal imaging revealed that Siglec-7+ MK-like cells displayed more elongated, highly branched mitochondrial networks than Siglec-7- one. In parallel, stored human platelets exhibited increased surface Siglec-7 expression. These findings identify Siglec-7 as a candidate regulator linking mitochondrial dynamics to MK differentiation and platelet function.
    Keywords:  Siglec-7; fission; fusion; megakaryocyte; mitochondrial dynamics
    DOI:  https://doi.org/10.1177/15473287261423853
  22. Clin Transl Med. 2026 Feb;16(2): e70619
       BACKGROUND: Acute pancreatitis (AP) is a severe inflammatory disorder in which mitochondrial dysfunction and ferroptosis critically drive acinar cell injury. Our previous work suggested a protective role for exogenous milk fat globule-epidermal growth factor 8 (MFG-E8) in AP. This study aimed to elucidate the molecular mechanism by which endogenous MFG-E8 mitigates mitochondrial damage and ferroptosis during AP.
    METHODS: Two mouse models of AP were used for in vivo studies, while cerulein + lipopolysaccharide-induced mitophagy and ferroptosis in AR42J cells (cells of the rat exocrine pancreas) for in vitro studies. Mfge8 gene-defective mice and lentivirus were utilised to downregulate MFG-E8 expression in mice and overexpress MFG-E8 in cells, respectively. Dual gene modification was employed to overexpress MFG-E8 and simultaneously knockdown adenosine triphosphate (ATP)-binding cassette subfamily E member 1 (ABCE1) in vitro. One mitophagy agonist and two ferroptosis inhibitors were used in both in vitro and in vivo experiments.
    RESULTS: Endogenous MFG-E8 expression was downregulated in experimental AP. Genetic deletion of Mfge8 aggravated mitochondrial ultrastructural damage, impaired mitophagy flux and intensified ferroptosis, as evidenced by increased lipid peroxidation, Fe2+ accumulation and depletion of glutathione peroxidase. Lentiviral overexpression of MFG-E8 in AR42J acinar cells restored mitophagy activity, preserved mitochondrial membrane potential and reduced oxidative stress. Mechanistically, co-immunoprecipitation confirmed that MFG-E8 directly interacts with ABCE1, a key mitophagy regulator. ABCE1 knockdown abolished the protective effects of MFG-E8 on mitochondrial function and ferroptosis suppression, indicating that the MFG-E8/ABCE1 axis is essential for maintaining mitophagy homeostasis. Pharmacological restoration of mitophagy or inhibition of ferroptosis rescued acinar cell injury caused by MFG-E8/ABCE1 dysregulation. In vivo, ferroptosis inhibition significantly improved pancreatic pathology and survival in Mfge8-deficient AP mice.
    CONCLUSION: Endogenous MFG-E8 protects against AP by binding ABCE1 to sustain mitophagy flux and inhibit ferroptosis. Targeting this axis offers a promising therapeutic strategy for mitigating pancreatic injury.
    KEY POINTS: Endogenous MFG-E8 is downregulated in acute pancreatitis (AP), disrupting MFG-E8/ABCE1 complex formation. MFG-E8/ABCE1 axis sustains Parkin-PINK1-mediated mitophagy to clear damaged mitochondria in pancreatic acinar cells. This axis suppresses ferroptosis by reducing Fe2+ accumulation and lipid peroxidation, alleviating AP-related pancreatic injury.
    Keywords:  ABCE1; MFG‐E8; acute pancreatitis; ferroptosis; mitophagy
    DOI:  https://doi.org/10.1002/ctm2.70619
  23. Ecotoxicol Environ Saf. 2026 Feb 13. pii: S0147-6513(26)00109-0. [Epub ahead of print]311 119780
      As an emerging environmental contaminant, N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine-quinone (6PPD-Q) poses a potential threat to public health. However, the potential link between 6PPD-Q exposure and bone health remains largely unexplored. This study aims to systematically investigate the toxic effects of 6PPD-Q on bone metabolism and elucidate the underlying mechanisms by integrating transcriptomic sequencing, network toxicology, single-cell RNA, Molecular docking, molecular dynamics with both in vivo and in vitro experiments. Integrative analysis converged on mitophagy as a central mechanism in 6PPD-Q-induced osteoporosis, with single-cell sequencing identifying bone marrow-derived mesenchymal stem cells (BMSCs) as the key cell type and revealing CX43, MMP2, PDGFRB, and FYN as the principal targets. Molecular docking and MD simulations confirmed the targeted binding of 6PPD-Q to CX43. RNA-seq analysis of rat tibiae validated the differential expression of CX43 and the critical role of mitophagy. Both in vivo and in vitro experiments demonstrated that 6PPD-Q-induced bone loss was associated with the downregulation of CX43 and concomitant mitophagy dysregulation. In conclusion, this study elucidates that 6PPD-Q induces bone loss was associated with the downregulation of CX43 and concomitant mitophagy dysregulation. Our work establishes a comprehensive mechanistic framework for 6PPD-Q-induced bone damage and offers novel insights for future research into its bone toxicity. The 1 or 10 mg/kg dose used in this study, although higher than the typical environmental exposure level, is consistent with the effects observed in cadmium exposure and is close to the 8 mg/kg dose used in studies on mouse bone toxicity. Additionally, the 5 ng/mL concentration of 6PPD-Q used in the in vitro experiments is comparable to the concentration detected in freshwater, indicating its environmental relevance.
    Keywords:  6PPD-Q; CX43; Mitophagy; Osteoporosis
    DOI:  https://doi.org/10.1016/j.ecoenv.2026.119780
  24. Theranostics. 2026 ;16(8): 4308-4335
      Mitophagy, a selective autophagic pathway that clears damaged or dysfunctional mitochondria, has emerged as a promising therapeutic approach. Mitophagy maintains a delicate balance between cell survival and death, while mounting evidence suggests that it predominantly promotes tumor cell survival under stress, particularly in responses to cancer therapy. Moreover, aberrant regulation of mitophagy results in cancer pathology with characteristic hallmarks, including remodeling of metabolic plasticity, maintenance of cancer stem cell characteristics, and immune regulation of the tumor microenvironment. This review synthesizes multifaceted roles of mitophagy in cancer biology, from tumor initiation and progression to therapy responses. It also summarizes molecular mechanisms underlying mitophagy. How cancer cells exploit mitophagy to survive therapy has been harnessed to develop therapeutic strategies. We elaborate the evolution of mitophagic therapy from small-molecule modulators to nanotechnology-based targeted delivery systems. Finally, we highlight the promise of targeting mitophagy in overcoming treatment resistance and improving clinical outcomes for patients.
    Keywords:  cancer therapy; mitophagy; nanotherapeutics; small molecule regulators
    DOI:  https://doi.org/10.7150/thno.129867
  25. Phytomedicine. 2026 Feb 13. pii: S0944-7113(26)00196-0. [Epub ahead of print]153 157959
       BACKGROUND: Osteoarthritis (OA) stands as a widespread joint condition that involves cartilage degeneration, meniscal injury, and synovial lesions, imposing a substantial economic and societal burden. Homoplantaginin (Homo), a flavonoid glycoside, is the primary active constituent of the traditional herbal medicine Salvia plebeia R.Br., and exhibits notable anti-inflammatory and anti-oxidative properties. Nevertheless, its therapeutic potential for OA remains largely unexplored.
    PURPOSE: This study aimed to evaluate the therapeutic efficacy of Homo in the treatment of OA and to elucidate its underlying mechanisms.
    STUDY DESIGN: By integrating in vivo and in vitro OA models, with transcriptomics analysis, molecular-protein affinity analysis, we identified the protective pathway implicated in the therapeutic mechanism of Homo against OA.
    METHODS: The therapeutic effect of Homo on OA was assessed using the anterior cruciate ligament transection (ACLT) mouse model in vivo and the LPS-induced chondrocytes model in vitro. Micro-CT and histological analysis were employed to evaluate the Homo's protective impacts on articular cartilage or subchondral bone in vivo. In vitro, CCK-8 assays, apoptosis analysis, Western blot, Real-time quantitative PCR (RT-qPCR), reactive oxygen species (ROS) staining assessed the Homo's influence on chondrocytes viability, oxidative stress, and extracellular matrix (ECM) metabolism. Subsequently, transcriptomics analysis, molecular docking, molecular dynamics simulations, cellular thermal shift assay (CETSA), and surface plasmon resonance (SPR) were performed to identify the potential therapeutic targets of Homo in OA. Furthermore, Western blot, RT-qPCR, immunofluorescence (IF), JC-1 staining, and Transmission electron microscope (TEM) were utilized to explore the modulation of Homo in mitochondrial function and mitophagy-related signaling pathways in chondrocytes.
    RESULTS: Homo significantly alleviated OA-related pathological manifestations in both in vivo and in vitro. These beneficial effects were evidenced by reduced cartilage degradation, normalized ECM metabolism, enhanced chondrocytes viability, suppression of apoptosis, and oxidative stress. Transcriptomics sequencing revealed mitophagy as a potential mechanism underpinning Homo's therapeutic action, accompanied by a marked upregulation of Sirt3 expression. Sirt3 was subsequently identified as a direct target protein of Homo via combined molecular docking, molecular dynamics simulations, CETSA, and SPR analysis. Further investigation demonstrated that Homo activates the Sirt3/PINK1/Parkin signaling pathway, thereby promoting mitophagy and restoring mitochondrial function. Ultimately, the therapeutic efficacy of Homo in ameliorating OA via targeting Sirt3 was conclusively validated through rescue experiments conducted in vivo and in vitro.
    CONCLUSION: This research elucidates that Homo ameliorates chondrocytes homeostasis and attenuates OA progression for the first time. We demonstrate that Homo directly binds to Sirt3, thereby activating the downstream PINK1/Parkin signaling axis and enhancing mitophagy. This finding provides an innovative therapeutic strategy for OA clinical management.
    Keywords:  Homoplantaginin; Mitophagy; Osteoarthritis; Sirt3/PINK1/Parkin signaling pathway
    DOI:  https://doi.org/10.1016/j.phymed.2026.157959
  26. Cardiovasc Drugs Ther. 2026 Feb 16.
      
    Keywords:  Ferroptosis; I/R injury; Ischemic cardiomyopathy; Mitochondria; Mitophagy
    DOI:  https://doi.org/10.1007/s10557-026-07839-w
  27. Food Res Int. 2026 Mar 31. pii: S0963-9969(26)00123-7. [Epub ahead of print]228 118449
      Previous epidemiological evidence has indicated that mushroom intake may reduce sarcopenia risk in older adults, though this is unconfirmed by laboratory studies. Here, we examined whether lentinan (LNT), a mushroom polysaccharide, influences C2C12 myoblast differentiation and attenuates age-related muscle atrophy in aged mice. In vitro, LNT significantly enhanced C2C12 differentiation, increasing myotube diameter and myogenic differentiation 1 (MyoD1)/myogenin expression. In vivo, LNT treatment enhanced grip strength and exercise endurance in naturally aging mice while also slowing muscle mass and cross-sectional area loss. Transmission electron microscopy analysis revealed that low and medium doses of LNT significantly increased mitochondrial abundance and improved mitochondrial morphology in both differentiated C2C12 and skeletal muscle tissues. Furthermore, the expression intensities of crucial proteins participating in mitochondrial biogenesis (PGC-1α, Nrf2, and TFAM) were significantly upregulated in cell samples. These results indicate that LNT may mitigate sarcopenia through activating the PGC-1α/Nrf2/TFAM and promoting mitochondrial biogenesis.
    Keywords:  Aging; C2C12; Mitochondrial; Mitochondrial biogenesis; Sarcopenia
    DOI:  https://doi.org/10.1016/j.foodres.2026.118449
  28. Adv Sci (Weinh). 2026 Feb 17. e21997
      Thioredoxin reductase 2 (TrxR2), a radical-trapping antioxidant, plays a critical role in cardiac defense. However, the mechanisms underlying its benefits remain unclear. In this study, we aimed to investigate whether endothelial TrxR2 prevents cardiac microvascular dysfunction in diabetic cardiomyopathy (DCM). Key genes in the thioredoxin family and those involved in ferroptosis were analyzed using bulk RNA-sequencing assay. Diabetic injury was induced in multiple transgenic mouse models, including endothelial cell-specific knockout mice for TrxR2, sterol carrier protein 2 (SCP2), and Tu translation elongation factor, mitochondrial (TUFM). The TrxR2 lactylation site was identified by mass spectrometry and verified by a custom-made lactylation antibody. Mitochondrial thioredoxin reductase (mitoTrxR) activity and lipid peroxyl radicals were detected using fluorescence staining. Endothelial TrxR2 deficiency significantly suppressed mitoTrxR activity, exacerbated cardiac microvascular dysfunction, and accelerated DCM progression. In contrast, TrxR2 overexpression and Kukoamine B (TrxR2 agonist) treatment inhibited mitochondria-associated ferroptosis by facilitating SCP2 degradation and blocking the mitochondrial translocation of acyl-CoA synthetase long-chain family member 4 (ACSL4) via mitophagy. Mechanistically, TrxR2 maintained TUFM expression by scavenging oxygen radicals, thereby facilitating the mitochondrial translocation of AMPK for mitophagy activation. TrxR2 undergoes lactylation at lysine 340. This process is mediated by mitochondrial alanyl-tRNA synthetase 2 (AARS2) and lactate accumulation in both human and mouse diabetic hearts. This modification and sodium lactate administration compensatorily enhanced mitoTrxR activity, promoted mitophagy, and conferred ferroptosis resistance in cardiac microcirculation in DCM. Our findings demonstrate that TrxR2 and its lactylation modification promote mitophagy, enhance ferroptosis resistance, and improve cardiac microvascular function in DCM. Thus, this study provides a promising therapeutic approach for the management of diabetic complications.
    Keywords:  Lactylation modification; TrxR2; diabetic cardiomyopathy; ferroptosis; mitophagy
    DOI:  https://doi.org/10.1002/advs.202521997
  29. Am J Physiol Endocrinol Metab. 2026 Feb 16.
      Polycystic ovary syndrome (PCOS) is a multifactorial endocrine disorder characterized by hyperandrogenism, inflammation, and ovarian dysfunction. While exercise has been recognized as an effective non-pharmacological strategy for managing PCOS symptoms, the molecular mechanisms underlying its therapeutic benefits remain unclear. In this study, we utilized a dehydroepiandrosterone-induced PCOS mouse model to investigate how aerobic exercise ameliorates ovarian pathology. Our results demonstrated that exercise restored the estrous cycle, reduced ovarian cyst formation, and alleviated ovarian fibrosis and inflammation. Exercise upregulated ATP-dependent protease Lon peptidase 1 (LONP1) expression, accompanied by normalization of key steroidogenic protein levels, cytochrome P450 side-chain cleavage enzyme (CYP11A1) and steroidogenic acute regulatory protein (StAR). In parallel, exercise activated AMP-activated protein kinase (AMPK), which was accompanied by restoration of LONP1-associated mitochondrial proteolytic capacity and normalization of steroidogenic enzyme turnover. Exercise also enhanced mitochondrial biogenesis related markers, including peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) and peroxisome proliferator-activated receptor-alpha (PPARα), suggesting improved mitochondrial homeostasis in the PCOS ovary.
    Keywords:  Exercise; Hyperandrogenism; Inflammation; Mitochondrial Proteostasis; PCOS; Steroidogenesis
    DOI:  https://doi.org/10.1152/ajpendo.00457.2025
  30. Front Genet. 2026 ;17 1760869
       Introduction: Ulcerative colitis (UC) is a lifelong, chronic inflammatory disorder, characterized by recurrent and diffuse inflammation of the rectal and colonic mucosa. Increasing evidence suggests that impaired mitophagy contributes to immune dysregulation and epithelial injury in UC. However, the mitophagy-related molecular landscape and its therapeutic potential remain largely unexplored.
    Methods: Mitophagy-related genes (MRGs) were intersected with differentially expressed genes to identify UC-associated MRGs. Functional enrichment, immune infiltration, and consensus clustering analyses were performed to characterize molecular subtypes. Three machine learning methods were employed to identify diagnostic models. Candidate therapeutic agents were identified by the CMap database.
    Results: A total of 35 UC-associated MRGs were identified, enriched in cell activation, fatty acid metabolism, and the PPAR signaling pathway, revealing strong immunometabolic coupling in UC. Consensus clustering stratified UC patients into two subtypes: a metabolism-dominant subtype (C1) and an inflammation-activated subtype (C2). Three hub genes-CD55, CPT1A, and SLC16A1-were screened and validated as robust diagnostic markers. Drug prediction and molecular docking revealed strong binding between galunisertib and CD55, which was further validated by molecular dynamics simulations. In vitro, galunisertib significantly suppressed inflammatory cytokine release in LPS-induced UC cell models.
    Discussion: This study delineated the mitophagy-related molecular signatures of UC and identified CD55, CPT1A, and SLC16A1 as key biomarkers linking mitochondrial dysfunction, metabolic reprogramming, and immune activation. Furthermore, galunisertib was proposed as a potential therapeutic agent, providing a theoretical basis for UC therapy.
    Keywords:  drug prediction; machine learning; mitophagy; molecular dynamic simulation; ulcerative colitis
    DOI:  https://doi.org/10.3389/fgene.2026.1760869
  31. Diabetes Obes Metab. 2026 Feb 19.
       AIMS: Growth differentiation factor 15 (GDF15) has emerged as a promising metabolic regulator with hepatoprotective properties in metabolic dysfunction-associated steatotic liver disease (MASLD), yet its underlying mechanisms remain elusive. Given that mitochondria are the primary site of fatty acid oxidation (FAO) and that mitochondrial morphodynamics are critical for normal hepatic lipid metabolism, we investigated how GDF15 regulates hepatic lipid homeostasis through mitochondrial dynamics.
    MATERIALS AND METHODS: We established cellular steatosis models using primary rat hepatocytes exposed to lipotoxic palmitate (PA) or non-lipotoxic free fatty acid mixture (FFA, oleate: palmitate = 2: 1). Following GDF15 administration, we quantified lipid droplet content, expression of lipid metabolism genes, mitochondrial fatty acid translocation, and mitochondrial morphodynamics and function. The mechanistic role of ERK1/2 signalling was assessed through pharmacological inhibition. These findings were subsequently validated in adult progenitor cell-derived human liver organoids.
    RESULTS: GDF15 significantly mitigated both PA- and FFA-induced lipid accumulation by upregulating key FAO genes and down regulating lipid synthesis genes. Importantly, GDF15 corrected PA-induced mitochondrial fusion-fission imbalance by increasing mitochondrial fusion proteins MFN1 and OPA1 while modulating the activation of fission regulator DRP1. GDF15 enhanced fatty acid translocation into mitochondria and improved FAO. Mechanistically, GDF15 exerted these effects partially through inhibition of the ERK1/2 signalling pathway. Human liver organoid models further corroborated this protective mechanism of GDF15 against hepatic steatosis.
    CONCLUSIONS: Our study reveals that, specifically under lipotoxic conditions, GDF15 alleviates hepatocyte steatosis by preserving mitochondrial morphodynamics homeostasis and enhancing mitochondrial FAO capacity via ERK1/2 inhibition. These condition-specific mechanisms provide critical insights into GDF15's hepatoprotective effects and support its further investigation as a potential therapeutic target for MASLD.
    Keywords:  GDF15; MASLD; lipid metabolism; mitochondrial morphodynamics
    DOI:  https://doi.org/10.1111/dom.70561
  32. Brain. 2026 Feb 19. pii: awaf261. [Epub ahead of print]
      Downregulation and inactivation of the Repressor Element 1-Silencing Transcription factor (REST) is shown in Alzheimer's disease (AD) and likely contributes to its progression, but the exact molecular mechanism linking REST reduction to AD remains unclear. We examined changes in REST expression in the entorhinal cortex and hippocampus across different Braak stages of tauopathy. We show that alterations in REST expression and sub-cellular localization are partially responsible for AD pathology, as REST overexpression improves cognition, reduces amyloid-β and phosphorylated Tau deposition, and restores mitochondrial and synaptic homeostasis. Mechanistically, the NAD+/SIRT1 axis modulates REST expression through chromatin remodelling in the promoter region of REST, leading to changes in the expression of REST target genes involved in mitophagy and synaptic function. These findings reveal a new mechanism of action for NAD+ and highlight REST as a promising therapeutic target for AD therapy.
    Keywords:  Alzheimer’s disease; NAD+; REST; SIRT1; dementia; mitophagy
    DOI:  https://doi.org/10.1093/brain/awaf261
  33. Free Radic Biol Med. 2026 Feb 18. pii: S0891-5849(26)00074-2. [Epub ahead of print]
       BACKGROUND: Pathological features of cardiovascular complications remain persistent in diabetic patients, even under strict blood glucose control. Hyperglycemia-induced metabolic memory (HIMM) in endothelial cells (ECs) is a significant contributor to this phenomenon, particularly through its effects on mitochondrial function. Arginase2 (Arg2), a mitochondrial enzyme, plays a crucial role in regulating mitochondrial and vascular homeostasis in various vascular diseases, but the role of endothelial Arg2 in HIMM remains unclear.
    METHODS: We established both in vivo (HIMM-mouse model) and in vitro (HIMM-EC model) systems to assess the activation status of arginase 2 (Arg2), alterations in arginine metabolism, and mitochondrial function. Endothelial- specific Arg2-overexpressing and knockout mice were generated to evaluate the critical role of Arg2 in cardiovascular function and HIMM-induced protection via ultrasound imaging system, laser speckle flowmetry, myograph, and immunofluorescence staining. Arg2- knockout/overexpression cell lines were established and mitochondrial function and its regulatory mechanisms in response to damage was assessed using MitoSOX, MitoTracker, oxygen consumption rate (OCR), and Western blot.
    RESULTS: We initially observed that HIMM triggered significant Arg2 activation, arginine metabolism dysregulation, mitochondrial dysfunction, and vascular impairment in both in vivo and in vitro models. Endothelial-specific Arg2 overexpression successfully recapitulated these pathological phenotypes, leading to endothelial damage and vascular dysfunction. Further we confirmed that endothelial Arg2 knockout effectively protected against HIMM-induced endothelial damage, mitochondrial hyper-fragmentation, and cardiac dysfunction. These improvements were mediated by correcting aberrant Arg2 expression, which restored arginine levels, activated the NO-cGMP-PKG signaling pathway, and ultimately suppressed excessive mitochondrial fission, leading to improved cardiovascular function.
    CONCLUSION: Our findings highlight the critical role of endothelial Arg2 in maintaining vascular homeostasis via arginine metabolism and mitochondrial fission. This identifies Arg2 as a promising therapeutic target for HIMM-related vascular diseases.
    Keywords:  Arginase 2; Arginine Metabolism; Hyperglycemia-induced metabolic memory; endothelial impairment; mitochondrial fission
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.01.054
  34. bioRxiv. 2026 Feb 12. pii: 2025.12.22.695711. [Epub ahead of print]
      Mitochondrial stress activates the integrated stress response (ISR) through the mitochondrial protein DELE1, which relays stress signals to the cytosolic kinase HRI to induce ATF4. Dysregulation of DELE1-mediated signaling has been implicated in pathological conditions, yet molecular strategies to modulate DELE1 remain unavailable. Here, we report de novo designed proteins that bind DELE1, block its oligomerization, and inhibit DELE1-mediated ISR activation. Several designs form stable complexes with DELE1 and disrupt its oligomerization in vitro while preserving DELE1's ability to bind HRI. In cells, these designs suppress ATF4 induction during mitochondrial stress and impair the recovery of elongated mitochondrial morphology following transient insult. Crystal structure analysis, structural modeling, and targeted mutagenesis confirm that the designed proteins engage a critical interface required for DELE1 oligomerization. These findings establish DELE1 as a druggable target and demonstrate that de novo designed proteins offer precise tools to modulate this pathway, laying groundwork for therapeutic development.
    DOI:  https://doi.org/10.64898/2025.12.22.695711
  35. Am J Nephrol. 2026 Feb 20. 1-17
      Sodium-glucose cotransporter 2 inhibitors (SGLT2is) have demonstrated renoprotective effects in chronic kidney disease (CKD), but their therapeutic potential in membranous nephropathy (MN) remains unclear. In this study, analysis of the GEO database revealed that CAV1 expression is significantly upregulated in MN, suggesting a potential role in disease progression. A rat MN model was induced with cationic bovine serum albumin (C-BSA) and treated with canagliflozin (10 mg/kg). Renal function and histopathological changes were assessed. In vitro, MPC-5 podocytes were injured with complement C5a and treated with canagliflozin or CAV1 overexpression to explore mechanisms related to mitochondrial fission and apoptosis. Canagliflozin treatment markedly reduced proteinuria, increased serum albumin, and improved renal histology, including attenuation of mesangial hyperplasia, basement membrane thickening, and subepithelial electron-dense deposits. It also restored the expression of podocyte markers nephrin and podocin, inhibited the CAV1/PKA/DRP1 signaling pathway, preserved mitochondrial membrane potential, reduced pro-apoptotic markers Bax and cleaved caspase-3, and upregulated the anti-apoptotic protein Bcl-2. These findings suggest that canagliflozin alleviates podocyte injury and renal damage in MN by suppressing mitochondrial fission and apoptosis through inhibition of the CAV1/PKA/DRP1 signaling axis.
    DOI:  https://doi.org/10.1159/000550928
  36. J Nutr. 2026 Feb 18. pii: S0022-3166(26)00076-3. [Epub ahead of print] 101427
       BACKGROUND: Mitochondrial dysfunction is recognized as a key pathophysiological mechanism in neurodegenerative diseases. Alterations in mitochondrial dynamics-including imbalances in fission and fusion, impaired biogenesis, and disrupted mitophagy-contribute to the onset and progression of neurological disorders. In this context, mitochondrial modulation has emerged as a promising therapeutic strategy.
    OBJECTIVE: This systematic review examined the role of riboflavin, a water-soluble vitamin and essential mitochondrial cofactor, in neurological interventions through mitochondrial modulation, with emphasis on elucidating the underlying molecular mechanisms.
    METHODS: A search of the PubMed, Embase, Scopus, and Web of Science databases identified 23 eligible studies, comprising 6 in vitro experiments, 10 rodent models, and 7 clinical trials.
    RESULTS: These studies evaluated the effects of riboflavin in monogenic, neurodegenerative, and demyelinating mitochondrial diseases, cerebrovascular/hypoxic injury, and pain/migraine. Clinical evidence indicated that riboflavin may regulate oxidative stress in stroke and perinatal asphyxia, with associated functional improvements. Preclinical findings revealed mechanisms of action involving energy homeostasis, cell cycle regulation, and mitochondrial dynamics across monogenic mitochondrial disorders, neurodegenerative diseases, hypoxic injury, and models of pain and migraine. Possibly through mitochondrial modulation, riboflavin appeared to reduce α-synuclein aggregation in Parkinson's disease, increase the number of tyrosine-hydroxylase-positive neurons in Alzheimer's disease models, enhance neuronal survival in Brown-Vialetto-Van Laere and Huntington's disease models, and normalize neuronal excitability in ataxia and migraine. In contrast, no therapeutic effects were observed in demyelinating diseases.
    CONCLUSIONS: Overall, the findings suggest that riboflavin may promote neuroprotection through redox modulation and gene regulation, stabilization of membrane potential, and enhanced mitochondrial complex activity via flavin cofactors, ultimately supporting neuronal metabolism and functional outcomes. Despite advances in mechanistic understanding, clinical applications in humans remain insufficiently defined for most conditions, with clearer dosage regimens currently established only for stroke and migraine.
    Keywords:  brain; degenerative diseases; mitochondria; mitochondrial biogenesis; vitamin B2
    DOI:  https://doi.org/10.1016/j.tjnut.2026.101427
  37. Autophagy. 2026 Feb 15. 1-23
      Recently, mitophagy-mediated bone mineralization of mesenchymal stem cells has emerged as another bone formation pattern, but whether mitophagy-mediated bone mineralization shapes craniofacial development remains unknown. Here, we demonstrate that loss of OPTN, a keystone macroautophagy/autophagy receptor, impairs mitophagy and acidic calcium phosphate (ACP) transport in orofacial bone mesenchymal stem cells (OMSCs), leading to craniofacial bone mineralization defects. We substantiate that OPTN undergoes LLPS both in vitro and in vivo, driven by S173 phosphorylation within its intrinsically disordered N-terminal domain (NTD), facilitating the association of OPTN complexes with phagophore membranes. Additionally, the ubiquitin-binding domain (UBD) in OPTN's C-terminal domain (CTD) also promotes LLPS to recruit ubiquitin-modified mitochondria. Physiochemically, mutations at the conserved sites in human OPTN (S173A and D474N) disrupt the OPTN LLPS, as validated in mouse and zebrafish, thereby inhibiting mitophagy and impairing bone mineralization. Together, our findings reveal a new mechanism through which OPTN LLPS couples mitophagy-mediated mineralization to craniofacial bone development, highlighting its potential as a therapeutic target for treating orofacial malformations via modulation of mitophagy.Abbreviations: 1, 6HD: 1, 6-hexanediol; ACP: acidic calcium phosphate; ALP: alkaline phosphatase; ARS: Alizarin Red staining; BFR/BS: bone formation rate per bone surface; Baf-A1: bafilomycin A1; CCCP: carbonyl cyanide 3-chlorophenylhydrazone; CTD: C-terminal domain; dpf: days post-fertilization; EDS: energy dispersive spectroscopy; FL: full length; FRAP: fluorescence recovery after photobleaching; hpf: 24h post-fertilization; IDR: intrinsically disordered region; IHC: immunohistochemistry; LLPS: liquid-liquid phase separation; LC-MS/MS: liquid chromatography-tandem mass spectrometry; MAR: mineral apposition rate; MS/BS: mineralizing surface per bone surface; NTD: N-terminal domain; ODM: osteogenic differentiation medium; OMSCs: orofacial bone mesenchymal stem cells; OPTN: optineurin; P1: postnatal day 1; P21: postnatal day 21; PDB: Paget disease of bone; PTMs: post-translational modifications; qRT-PCR: quantitative real-time PCR; S173: serine 173; STK4: serine/threonine kinase 4; SEM: scanning electron microscopy; TMD: tissue mineral density; TEM: transmission electron microscopy; UBD: ubiquitin-binding domain; Ub: ubiquitin.
    Keywords:  Bone mineralization; OPTN; craniofacial development; mitophagy; phase separation
    DOI:  https://doi.org/10.1080/15548627.2026.2624745
  38. Biomaterials. 2026 Feb 11. pii: S0142-9612(26)00085-2. [Epub ahead of print]330 124061
      Oxidative stress-induced enteric neuropathy is a key driver of slow-transit constipation (STC), primarily through disrupted mitochondrial dynamics and neuronal degeneration. To address this, we developed a bioengineered oral delivery system that supports neuronal recovery and actively enhances mitochondrial membrane fusion. A self-assembling amphiphilic peptide (GFF) was synthesized to encapsulate rhein (RH), a natural anthraquinone with antioxidant, anti-inflammatory, and microbiota-regulating properties. A BDNF-derived tetrapeptide was integrated to further potentiate neurotrophic effects. These components were co-assembled into a therapeutic nanofiber (RFI), which was embedded in a chitosan/sodium alginate hydrogel for sustained oral delivery. In vitro and in vivo studies demonstrated that RFI significantly improved neuronal viability and gastrointestinal motility. Mechanistic investigations revealed that RFI is associated with activation of the AKT signaling pathway and enhancement of mitochondrial membrane fusion, collectively contributing to the restoration of mitochondrial network integrity and neuronal protection. This multifunctional nanoplatform offers a promising therapeutic approach to STC by combining targeted delivery with direct modulation of mitochondrial function.
    Keywords:  Bioinspired peptide hydrogel; Colon-targeted oral delivery; Mitochondrial fusion modulation; Peptide–drug conjugate; Self-assembling peptide nanofiber
    DOI:  https://doi.org/10.1016/j.biomaterials.2026.124061
  39. Cancer Biol Med. 2026 Feb 17. pii: j.issn.2095-3941.2025.0360. [Epub ahead of print]
       OBJECTIVE: Paclitaxel (PTX), a conventional second-line therapeutic agent for advanced gastric cancer (GC), exhibits compromised clinical efficacy due to acquired chemoresistance in patients, the molecular mechanisms of which remain poorly elucidated. This study aimed to investigate the therapeutic potential of targeting extracellular vesicle (EV) protein in reversing PTX resistance in GC cells and to delineate the underlying molecular pathways involved.
    METHODS: Proteomic profiling was used to identify differentially expressed EV proteins in PTX-resistant GC cells. EVs were isolated via size exclusion chromatography (SEC) and characterized using transmission electron microscopy (TEM), nano-flow cytometry (nano-FCM), and western blot analysis. In vivo functional validation was performed in xenograft tumor models by injecting EV proteins into nude mice via the tail vein (6 groups, n = 4). EVs derived from 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS)-treated cells were administered to tumor-bearing nude mouse model (4 groups, n = 5) to determine the impact of EV-derived voltage-dependent anion channel protein 1 (VDAC1) on PTX resistance. In addition, VDAC1 protein expression was evaluated using immunohistochemical (IHC) assays in 34 clinical specimens from PTX-resistant patients.
    RESULTS: Proteomic analyses demonstrated a marked upregulation of VDAC1 in EVs secreted by PTX-resistant GC cells. Functional studies revealed that intercellular transfer of EV-derived VDAC1 directly conferred PTX resistance to drug-sensitive cancer cells. Gene set enrichment analysis (GSEA) and adenosine triphosphate (ATP) functional assay further elucidated that VDAC1-mediated chemoresistance was mechanistically linked to the activation of adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) signaling and concomitant suppression of the mammalian target of rapamycin - p70 ribosomal protein S6 kinase (mTOR-p70S6K) pathway. In vivo validation confirmed that systemic delivery of EV-derived VDAC1 significantly reduced PTX sensitivity in GC tumors. Furthermore, DIDS inhibited the expression of the VDAC1 protein in EVs, thereby reducing PTX resistance in vivo and in vitro. IHC analysis revealed that VDAC1 expression was significantly higher in GC patients with PTX resistance compared to PTX-sensitive patients.
    CONCLUSIONS: The findings herein underscore the pivotal role of EV-derived VDAC1 in driving PTX resistance in GC through dual modulation of autophagy and mitophagy, mediated by the AMPK/mTOR signaling axis. Targeting EV-derived VDAC1 has emerged as a promising therapeutic strategy to counteract chemoresistance, providing a novel avenue for improving GC treatment outcomes.
    Keywords:  Extracellular vesicles; autophagy; gastric cancer; mitophagy; paclitaxel-resistance; voltage-dependent anion channel protein 1
    DOI:  https://doi.org/10.20892/j.issn.2095-3941.2025.0360
  40. Ocul Surf. 2026 Feb 13. pii: S1542-0124(26)00022-4. [Epub ahead of print]40 117-129
       PURPOSE: To investigate the expression and role of translocator protein (TSPO) in dry eye disease (DED).
    METHODS: In vitro experiments were performed using immortalized human corneal epithelial cells (HCECs) cultured under hyperosmolar conditions (500 mOsM). Cell viability was analyzed by the Cell Counting Kit-8 assay. Intracellular reactive oxygen species (ROS) generation was detected by 2',7'-dichlorodihydrofluorescein diacetate staining. Mitochondrial membrane potential was assessed using the JC-1 assay. Intracellular calcium (Ca2+) levels were measured by Fluo-4 AM staining. Apoptosis was analyzed by flow cytometry. Mitochondrial morphology was observed using transmission electron microscopy. mRNA expression was quantified by real-time PCR. Protein expression was assessed by western blotting, enzyme-linked immunosorbent assay, and immunofluorescence. In vivo experiments were conducted using a scopolamine-induced DED model in female Wistar rats. Clinical parameters of tear secretion, corneal epithelium defects, and conjunctival goblet cells density were measured. mRNA and protein expression in the cornea and conjunctiva were assessed by real-time PCR, western blotting, and immunofluorescence. Apoptosis in the cornea and conjunctiva was assessed by TUNEL staining.
    RESULTS: In vitro, TSPO was overexpressed in HCECs exposed to hyperosmotic stress, accompanied by elevated levels of pro-inflammatory cytokines, ROS overproduction, intracellular Ca2+ overload, and mitochondrial dysfunction, ultimately leading to apoptosis. TSPO knockdown significantly enhanced cell survival by attenuating these cellular injuries and inhibiting apoptosis via a mitochondria-dependent pathway. In vivo, increased TSPO expression was observed in both the corneal and conjunctival tissues of DED rats, along with elevated inflammation. Treatment with the TSPO-specific ligand PK11195 significantly antagonized TSPO expression, alleviated inflammation, preserved corneal epithelial integrity, and suppressed apoptosis without reversing tear deficiency.
    CONCLUSIONS: TSPO overexpression participates in the pathogenesis of DED. Inhibiting TSPO alleviates inflammation and oxidative stress and promotes cell survival through a mitochondrial-dependent pathway.
    Keywords:  Apoptosis; Dry eye; Inflammation; Mitochondrial dysfunction; PK11195; Translocator protein (TSPO)
    DOI:  https://doi.org/10.1016/j.jtos.2026.02.005
  41. J Agric Food Chem. 2026 Feb 17.
      This study investigated the therapeutic potential of eicosapentaenoic acid (EPA) against type 2 diabetes mellitus (T2DM)-related sarcopenia. In a streptozotocin/high-fat diet-induced T2DM mouse model, 24 week EPA supplementation improved insulin resistance, reduced advanced glycation end product (AGE) accumulation, and preserved skeletal muscle mass and strength. In vitro, the EPA mitigated high-glucose/AGE-induced atrophy in C2C12 myotubes. Mechanistically, EPA counteracted T2DM-related sarcopenia through improving insulin resistance and glycemic control, lowering AGE accumulation, and attenuating inflammatory response and oxidative damage in skeletal muscle. Moreover, EPA protected mitochondrial integrity in skeletal muscle cells by activating the AMPK/Sirt1/PGC-1α axis to boost mitochondrial biogenesis and alleviated excessive apoptosis via inhibiting the intrinsic apoptotic pathway. Furthermore, the EPA maintained protein metabolic homeostasis in skeletal muscle via restoring the PI3K/Akt/mTOR signaling cascade and suppressing the FoxO3a- and NF-κB-mediated ubiquitin-proteasome pathway. Overall, our findings suggest EPA as a promising nutritional intervention against T2DM-related sarcopenia.
    Keywords:  EPA; T2DM; mitochondrial quality; protein metabolic homeostasis; sarcopenia
    DOI:  https://doi.org/10.1021/acs.jafc.5c11649
  42. Biol Trace Elem Res. 2026 Feb 19.
      Lead (Pb), a persistent and highly toxic environmental contaminant, induces severe multi-organ toxicity, with the liver as a primary target. Naringenin (Nar), a natural flavonoid with established antioxidant properties, shows potential in mitigating chemical-induced liver injury; however, its protective mechanism against Pb hepatotoxicity remains unclear. This study investigated the hepatoprotective effects and underlying mechanisms of Nar in Pb-exposed rats. Thirty-six five-week-old male Sprague-Dawley rats were randomly assigned to six groups (n = 6): control, three Pb-treated groups (15, 30, and 60 mg/kg), co-treatment group (60 mg/kg Pb + 50 mg/kg Nar), and Nar-alone group (50 mg/kg). After 8 weeks, Pb exposure induced significant liver injury, evidenced by histopathological lesions (e.g., central venous congestion and inflammation), elevated serum levels of ALT, AST, and LDH, and oxidative stress (increased MDA; decreased CAT, T-SOD, and GSH). At the molecular level, Pb exposure suppressed the Nrf2/NQO1 pathway, upregulated Keap1, and impaired autophagic flux, as indicated by a decreased LC3-II/LC3-I ratio, accumulated p62, and a disrupted PINK1/Parkin pathway. Corroborating the impaired flux, transmission electron microscopy (TEM) revealed an accumulation of autophagic vacuoles, indicative of blocked autophagic degradation. Crucially, Nar co-treatment effectively mitigated these Pb-induced disturbances by activating the Nrf2/NQO1 pathway to counteract oxidative stress and restored autophagic flux, which was supported by the reversal of p62 accumulation and normalization of the LC3-II/LC3-I ratio. In conclusion, Nar protects against Pb-induced hepatotoxicity by concurrently alleviating oxidative stress and restoring autophagic function, supporting its potential as a therapeutic agent.
    Keywords:  Autophagy; Lead toxicity; Liver injury; Mitophagy; Naringenin; Oxidative stress
    DOI:  https://doi.org/10.1007/s12011-026-05023-7
  43. Free Radic Biol Med. 2026 Feb 16. pii: S0891-5849(26)00138-3. [Epub ahead of print]
       OBJECTIVE: Mitochondrial dysfunction and dysregulated cell death are key drivers of diabetic kidney disease (DKD) progression. This study aimed to construct CD44-targeted chitosan (Cs) nanoparticles encapsulating ginsenoside Rg1 (CD44-Cs@Rg1) for targeted delivery, and to evaluate their ability to regulate autophagy, pyroptosis, and mitochondrial function in DKD.
    METHODS: CD44-Cs@Rg1 nanoparticles were synthesized using a covalent modification strategy. Their targeting uptake, effects on GSDMD-mediated pyroptosis, autophagic flux, and energy metabolism were systematically evaluated in renal tubular epithelial cells under high-glucose (HG) conditions and in DKD mouse models. Mitochondrial function was assessed by Western blotting, immunostaining, MitoSOX, JC-1, and ATP assays. Transcriptomic profiling and pharmacological interventions were applied to elucidate the involvement of the AMPK/mTOR signaling axis.
    RESULTS: CD44-Cs@Rg1 nanoparticles were efficiently internalized by renal tubular epithelial cells, significantly reducing pyroptosis while restoring autophagic flux through AMPK activation and mTOR inhibition. These effects improved mitochondrial membrane potential, reduced reactive oxygen species accumulation, and enhanced ATP production. In vivo, CD44-Cs@Rg1 treatment markedly ameliorated renal dysfunction and histopathological injury in DKD mice. Transcriptomic and protein-level analyses consistently revealed enrichment of pathways related to AMPK signaling, autophagy, and energy metabolism.
    CONCLUSION: CD44-targeted Cs nanoparticles enable precise delivery of ginsenoside Rg1 to renal tubular cells in DKD, restoring mitochondrial homeostasis and regulating autophagy-pyroptosis balance via the AMPK/mTOR axis. This nanotherapeutic platform demonstrates strong translational potential for DKD treatment.
    Keywords:  AMP-Activated Protein Kinase/Mammalian Target of Rapamycin Signaling Axis; Autophagy and Pyroptosis; CD44-Targeted Chitosan Nanoparticles; Diabetic Kidney Disease; Ginsenoside Rg1; Mitochondrial Functional Homeostasis
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.02.041
  44. Free Radic Biol Med. 2026 Feb 17. pii: S0891-5849(26)00126-7. [Epub ahead of print]
      Myocardial ischemia (MI) remains a major global health challenge, with prevailing therapies inadequately addressing the critical link between metabolic dysfunction and structural remodeling. Ginsenoside CK (CK), a bioactive natural product, has shown cardioprotective effects, yet its precise molecular targets and mechanisms are not fully elucidated. This study employed an integrated multi-omics approach, combined with in vitro and in vivo validation and gene-editing techniques, to systematically investigate the pathogenesis of MI and the therapeutic basis of CK. Our findings indicate that the matricellular protein Sparc acts as a significant pathogenic driver in MI. We characterized the Sparc-p62 interaction axis, where Sparc directly interacts with the autophagy adaptor p62. This interaction triggers a series of harmful events, including severe disruption to the flux of mitochondrial autophagy, secondary mitochondrial dysfunction, the release of reactive oxygen species and the activation of inflammatory pathways. Ultimately, this leads to injury to the cardiomyocytes and abnormal extracellular matrix remodelling. CK was found to directly bind to Sparc, competitively inhibiting its role in overexciting p62. This effectively disrupts the pathogenic axis. Consequently, CK unblocks the degradation of inhibited mitochondrial autophagy streams, restores mitochondrial bioenergetics, and alleviates oxidative stress and inflammation. The results in a delay in the fibrosis process and a substantial improvement in cardiac function. The research identified the interaction between Sparc and p62 as a potential mechanism underlying MI injury and demonstrated the potential of CK to inhibit this pathway. It providing a scientific foundation for subsequent drug and mechanism research.
    Keywords:  Extracellular matrix; Ginsenoside CK; Mitochondrial autophagy; Myocardial ischemia; Oxidative damage; Sparc; p62
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.02.029
  45. Cell Metab. 2026 Feb 17. pii: S1550-4131(26)00012-4. [Epub ahead of print]
      Endothelial cells (ECs) are key metabolic gatekeepers, yet their role in metabolic health remains unclear. Given their central involvement in energy metabolism, mitochondria are ideally positioned to enable ECs to adapt to ever-changing metabolic requirements. Here, we explore the hypothesis that mitochondrial dynamics proteins in ECs influence whole-body metabolic status. Genetic deficiency of Mfn2 in ECs (Mfn2iΔEC), but not of Mfn1iΔEC, induces a mitohormetic response in the adipose vasculature, enhancing antioxidant defenses, mitochondrial fitness, and lipid oxidation, ultimately improving metabolic outcomes. Cultured ECs secrete the mitokine growth differentiation factor 15 (GDF15) via a forkhead box O1 (FOXO1)-dependent axis, a response also observed under stress conditions in vivo. Notably, Mfn2iΔEC mice exhibited elevated endothelial and circulating GDF15 levels, and neutralization of GDF15 partly attenuated their metabolic benefits. Consistent with mitohormetic activation, Mfn2iΔEC mice showed protection against diet-induced obesity and delayed age-related decline. Hence, vascular mitohormetic adaptations emerge as a novel mechanism promoting systemic metabolic health.
    Keywords:  GDF15; aging; diabetes; endothelial cells; mitochondria; mitofusin; mitohormesis; obesity
    DOI:  https://doi.org/10.1016/j.cmet.2026.01.012