bims-celmim Biomed News
on Cellular and mitochondrial metabolism
Issue of 2026–05–31
twenty papers selected by
Marc Segarra Mondejar, AINA



  1. Anal Chim Acta. 2026 Aug 08. pii: S0003-2670(26)00568-4. [Epub ahead of print]1410 345618
       BACKGROUND: Mitochondrial dysfunction and dysregulated enzymatic activity are hallmarks of liver cancer progression. Mitochondrial viscosity reports changes in the organelle microenvironment, whereas nitroreductase (NTR) activity is closely associated with tumor hypoxia and metabolic reprogramming. However, few probes enable reliable, simultaneous readout of both biomarkers in living systems. A robust fluorescent tool for dual-parameter imaging of mitochondrial viscosity and NTR activity would facilitate mechanistic studies and support potential tumor diagnosis.
    RESULTS: A novel naphthalimide-based bifunctional fluorescent probe, NCN-NTR, was designed and synthesized for the highly sensitive and simultaneous detection of mitochondrial viscosity and NTR activity in living systems via dual-emission channels. NCN-NTR displays a significant red fluorescence enhancement at 640 nm under high-viscosity conditions due to restricted intramolecular rotation, and exhibits a distinct 445 nm fluorescence at 390 nm upon NTR-mediated cleavage. The probe shows excellent selectivity, photostability, and pH tolerance, enabling reliable imaging in complex biological systems. Confocal microscopy confirmed its mitochondrial localization and enabled visualization of microenvironmental changes during hypoxia and starvation. Importantly, the probe effectively discriminated cancer cells from normal cells and produced rapid, tumor-associated fluorescence signals in vivo. These results collectively highlight the probe's capacity for sensitive, real-time dual-modal bioimaging.
    SIGNIFICANCE: NCN-NTR integrates organelle targeting with dual-emission sensing to simultaneously report mitochondrial viscosity and NTR activity in real time. Its performance in cellular and in vivo models highlights its potential for mechanistic studies of tumor-associated microenvironmental alterations and for precision fluorescence imaging with potential applications in cancer diagnosis.
    Keywords:  Fluorescent probe; In vivo imaging; Living cell imaging; Nitroreductase
    DOI:  https://doi.org/10.1016/j.aca.2026.345618
  2. Metabolites. 2026 May 12. pii: 321. [Epub ahead of print]16(5):
      Glycolysis and the pentose phosphate pathway (PPP) are two metabolic pathways that play crucial roles in brain energy metabolism. The glycolytic pathway is differentially regulated in neurons compared to astrocytes. In neurons, the flux directly through the glycolytic pathway is reduced due to compromised ability to activate the key glycolytic enzyme 6-phosphofructo-1-kinase (PFK1). Consequently, potential increases in neuronal glucose metabolic flux can occur through the PPP, leading to the generation of NADPH, which is essential for the antioxidant defense system in these cells. Additionally, the PPP can supply glycolysis with intermediates downstream of PFK1, resulting in the production of pyruvate, which is used by mitochondria for oxidative phosphorylation and ATP production. In this review, we propose that during increased activity, neurons will preferentially metabolize glucose through the PPP. This allows them to support their antioxidant defense mechanisms and maintain bioenergetic metabolism by bypassing the limiting PFK1 enzyme and still forming pyruvate for mitochondrial oxidation.
    Keywords:  astrocytes; glucose metabolism; glycolysis; neurons; pentose-phosphate pathway; pyruvate
    DOI:  https://doi.org/10.3390/metabo16050321
  3. J Photochem Photobiol B. 2026 May 20. pii: S1011-1344(26)00123-5. [Epub ahead of print]280 113476
      Fluorescence lifetime imaging microscopy (FLIM) using endogenous fluorescence of NADH (reduced nicotinamide adenine dinucleotide) and its phosphorylated form NADPH represents a powerful tool for monitoring cellular metabolic states. For a more nuanced interpretation of the FLIM data, investigating NAD(P)H in different cell compartments is crucial. In this study, we demonstrate that a weak NAD(P)H fluorescence in cell nuclei, which is often ignored, can be reliably analyzed using a phasor plot approach and provides a sensitive readout of metabolic responses. Using colorectal cancer cells HCT116 treated with the metabolic inhibitors rotenone and 3-bromopyruvate, as well as the chemotherapeutic agent 5-fluorouracil (5-FU), we show that nuclear NAD(P)H fluorescence decay changes in response to treatment. In the case of 5-FU, the phasor analysis of nuclear NAD(P)H reveals heterogeneous cellular responses with two subpopulations differing in NAD(P)H fluorescence decay parameters, fluorescence intensity, and cytoplasm-to-nucleus intensity ratio. Notably, nuclear and cytoplasmic responses are strongly correlated, indicating tight coupling of their NAD(P)H pools. Overall, our results establish nuclear NAD(P)H fluorescence as a robust, label-free indicator of cellular metabolism and highlight its potential for metabolic monitoring in conditions where analysis of NAD(P)H fluorescence is limited by spectral overlap with exogenous fluorescent labels.
    Keywords:  Cells response; Chemotherapy; FLIM; Fluorescence lifetime; NAD(p)h; Nuclei fluorescence; Phasor analysis
    DOI:  https://doi.org/10.1016/j.jphotobiol.2026.113476
  4. J Biol Chem. 2026 May 25. pii: S0021-9258(26)02065-X. [Epub ahead of print] 113193
      The hypoxia-inducible factor-1α (HIF-1α) has canonically been described as a primary regulator of glucose metabolism in hypoxic cells through transcriptional upregulation of all 10 glycolytic enzymes. Here, using 13C-glucose and 13C-glutamine tracing in intestinal epithelial cells with defined HIF1A genetic perturbations, we demonstrate that hypoxia-induced glycolysis can occur independently of HIF-1-driven transcription. While hypoxia modulates glucose-derived carbon flux into anabolic branches of glycolysis independent of HIF-1α, HIF-1α plays an important role in modulating glucose and glutamine utilisation within the TCA cycle. These alterations in substrate utilisation highlight the layered regulatory framework whereby HIF-1α regulates distinct aspects of glucose and glutamine metabolism in intestinal epithelial cells to impact the rate of intestinal epithelial cell growth and promote metabolic adaptation to hypoxia.
    Keywords:  HIF-1; Hypoxia; TCA cycle; glucose metabolism; glycolysis; metabolomics
    DOI:  https://doi.org/10.1016/j.jbc.2026.113193
  5. bioRxiv. 2026 May 18. pii: 2026.05.13.723899. [Epub ahead of print]
      Metabolic homeostasis has been studied primarily at the tissue and organism level, identifying molecular control mechanisms such as the energy charge-sensing kinase AMPK. Feedback loops involving AMPK and other regulators align cellular ATP generation and consumption, determining energetic balance. Recent work has demonstrated surprising oscillatory dynamics in AMPK activity, revealing unidentified kinetic modulation in single-cell homeostatic behaviour. However, probing the kinetic mechanisms of intracellular feedback requires simultaneous observation of multiple energetic parameters, and such experiments are precluded by the shared wavelength band occupied by most metabolic biosensors. We have overcome this obstacle by constructing a red-shifted FRET-based AMPK activity biosensor, RAMPKAR2, that is comparable to existing FRET-based AMPK activity biosensors. Multiplexed imaging of RAMPKAR2 with PercevalHR, which detects ATP/ADP ratio, confirmed that the kinetics of AMPK activity and ATP/ADP ratio are tightly coupled, with a lag of less than 6 minutes at the single-cell level. Pairing of RAMPKAR with HYlight, which detects the glycolytic intermediate fructose 1,6-bisphosphate (FBP), revealed that glycolytic activity co-oscillates with AMPK, shifted by ∼1.5 hours, and that these oscillations are suppressed by sustained AMPK activity. Together these data advance a model in which temporally offset increases in glycolytic ATP supply and AMPK deactivation contribute to single-cell oscillations.
    DOI:  https://doi.org/10.64898/2026.05.13.723899
  6. bioRxiv. 2026 May 17. pii: 2026.05.15.725497. [Epub ahead of print]
      Along with the membrane potential and respiration, mitochondrial matrix volume is a critical parameter that determines mitochondrial function. Mitochondria undergo constant changes in matrix volume and cristae dynamics, and in processes that are critical for normal metabolic rates and pathophysiological responses. Changes in matrix volume cannot be easily measured by conventional fluorescence imaging techniques due to the size of the sub-organellar structures, which are below resolution. This challenge was successfully resolved in studies of isolated mitochondria with the use of scattered light. Here we use dark-field imaging, which relies on scattered light contrast, to measure matrix volume dynamics in living cells. We demonstrate that mitochondrial volume changes can be easily detected as changes in intensity of the scattered light following matrix volume modulation with K + ionophores or by onset of the permeability transition. Specifically, we found that stimulation of K + influx leads to increase of mitochondrial matrix volume while stimulation of K + efflux leads to matrix shrinkage, and that activation of the permeability transition leads to high-amplitude mitochondrial swelling in wild-type but not in cells lacking subunit c of ATP synthase. These results directly demonstrate the dynamic nature of mitochondrial matrix volume and its link to physiological and pathological ion transport.
    DOI:  https://doi.org/10.64898/2026.05.15.725497
  7. Biomolecules. 2026 Apr 30. pii: 664. [Epub ahead of print]16(5):
      The differentiation of dental papilla cells (DPCs) into functional odontoblasts is critical for dentinogenesis, yet the role of mitochondrial dynamics remains unclear. Here, we investigated the functional role of mitochondrial fission and mitochondria-associated endoplasmic reticulum membranes (MAMs) in the odontogenic differentiation of DPCs. Using in vitro differentiation models combined with confocal microscopy, transmission electron microscopy, and gain- and loss-of-function approaches, we found that odontogenic induction triggered early mitochondrial fragmentation and increased MAM formation. Dynamin-related protein 1 (DRP1) mediated mitochondrial fission, which in turn regulated MAM architecture and promoted differentiation. Malic enzyme 2 (ME2) acted as an upstream regulator, facilitating DRP1 recruitment and organizing MAM integrity. Notably, disruption of the ME2-DRP1-MAM axis impaired dentin formation both in vitro and in vivo, either by ME2 knockdown or pharmacological inhibition of DRP1 (Mdivi-1). These findings establish the ME2-DRP1-MAM axis as a critical metabolic-organellar switch driving odontoblast differentiation, providing new mechanistic insights into dentinogenesis and identifying potential therapeutic targets for dentin-pulp complex regeneration.
    Keywords:  dental papilla cells; dynamin-related protein 1; malic enzyme 2; mitochondria-associated endoplasmic reticulum membranes; mitochondrial fission; odontogenic differentiation
    DOI:  https://doi.org/10.3390/biom16050664
  8. Commun Biol. 2026 May 29.
      The roles of glutamic-oxaloacetic transaminase 2 (GOT2) in malate-aspartate shuttle (MAS), fatty acid binding/trafficking, and peroxisome proliferator-activated receptor (PPAR) delta axis have been documented. However, its function in ferroptosis remains unexplored. Here, we report that GOT2 promotes ferroptosis by disturbing mitochondrial redox homeostasis through inhibiting the synthesis of radical scavenger coenzyme Q10 (CoQ10). Mechanism, by fueling MAS, GOT2 increases net influx of NADH into mitochondria and enhances aerobic respiration, increasing cellular ATP generation. The high ATP/ADP ratio inactivates adenosine 5'-monophosphate-activated protein kinase (AMPK) and PPARα, downregulating the transcription of core enzymes in CoQ10 synthesis pathway (FDPS, PDSS1/2, COQ3/5/6). In lung adenocarcinoma (LUAD), high expression of GOT2 restrains tumor progression by activating ferroptosis and igniting antitumor immunity. Whereas, the activation of GOT2-mediated ferroptosis exacerbates lesion in atherosclerosis disease. Our study reveals that GOT2-AMPK-PPARα-CoQ10 axis is a novel pro-ferroptosis pathway, and modulating GOT2-mediated ferroptosis suggests an intriguing method to treat LUAD and atherosclerosis.
    DOI:  https://doi.org/10.1038/s42003-026-10365-y
  9. Elife. 2026 May 26. pii: RP109206. [Epub ahead of print]14
      Metabolic dysfunction-associated steatotic liver disease (MASLD) progression is characterized by hepatic inflammation and cell death, yet the mechanisms underlying Kupffer cell (KC) loss remain poorly understood. Here, we sought to elucidate the metabolic basis of KC death during MASLD. Using metabolomics, immunostaining, and flow cytometry, we evaluated metabolic alterations and KC death throughout early MASLD progression. We found that KC death is an early hallmark of MASLD, exhibiting greater susceptibility and a spatial distribution consistent with KC zonation. Moreoever, KCs undergo progressive metabolic reprogramming toward enhanced glucose utilization during MASLD development, which is correlated with KC death. In combination with biochemical agonist, isotope tracing, and primary KC culture, we further demonstrated that augmented glycolytic metabolism directly drives KC death in vitro. Consistently, using Chi3l1-deficient mice, we further demonstrated that increased glucose utilization accelerates KC death in vivo. Together, these findings establish a causal link between glycolytic activation and KC loss during MASLD progression, highlighting glucose metabolic pathways as potential therapeutic targets to preserve KC homeostasis and mitigate MASLD.
    Keywords:  Kupffer cells; MASLD; cell death; glycolytic metabolism; medicine; metabolic reprogramming; mouse
    DOI:  https://doi.org/10.7554/eLife.109206
  10. Cell Rep. 2026 May 28. pii: S2211-1247(26)00541-3. [Epub ahead of print]45(6): 117463
      Mitophagy and xenophagy, two selective autophagy pathways sharing common E3 ligases, have been proposed to intersect in host defense against invading pathogens. Here, we show that mitochondrial damage, but not mitophagy, is essential for triggering xenophagy via the inner mitochondrial membrane protein prohibitin 2 (PHB2). Upon bacteria-induced disruption of the outer mitochondrial membrane, PHB2 bridges mitochondria to bacteria by binding bacterial surface proteins, while concurrently interacting with either auto-ubiquitinated E3 ligase ARIH1 or Parkin, two well-characterized mitophagy-associated E3 ligases. This interaction positions polyubiquitin chains near PHB2-targeted bacteria to recruit selective autophagy receptors for initiating xenophagy, leading to the co-autophagic degradation of bacteria and mitochondria, a process unaffected by mitophagy inhibition. Our findings establish an uncovered mechanism of mitochondria-dependent antibacterial autophagy, positioning mitochondrial PHB2 as both a bacterial sensor and an E3 ligase scaffold, and unveiling a previously unidentified process governing the recruitment of mitophagy-associated E3 ligases to intracellular bacteria.
    Keywords:  ARIH1; CP: cell biology; CP: molecular biology; Listeria; PHB2; Salmonella; Staphylococcus aureus; mitochondria; mitophagy; parkin; ubiquitin; xenophagy
    DOI:  https://doi.org/10.1016/j.celrep.2026.117463
  11. Cell Death Differ. 2026 May 27.
      Mitochondrial Ca2+ uptake shapes cellular signaling by modulating metabolism, cell death and cytosolic Ca2+ dynamics, yet its pathological and therapeutic relevance remains undefined. Here, we show that Ca2+ entry through the mitochondrial Ca2+ uniporter (MCU) is required for mitochondrial fragmentation and subsequent NLRP3 inflammasome-mediated IL-1β release in lipopolysaccharide-primed, stimulated macrophages. This fragmentation occurs independently of the mitochondrial permeability transition pore but depends on activation of the organelle fission machinery. In an inflammatory disease model, MCU deficiency attenuated IL-1β secretion and reduced monosodium urate (MSU) crystal-induced joint inflammation in vivo. Collectively, our findings establish mitochondrial Ca2+ uptake as a key upstream signal that promotes organelle fragmentation to license inflammasome activation, positioning MCU as a potential therapeutic target in inflammatory diseases.
    DOI:  https://doi.org/10.1038/s41418-026-01769-8
  12. Mol Cell. 2026 May 29. pii: S1097-2765(26)00310-2. [Epub ahead of print]
      Nearly all cellular processes are pH dependent. The acidic pH inside the lysosome (vacuole in yeast) is essential for cellular content degradation, signaling, and autophagy. Defects in lysosome/vacuole acidification are a conserved hallmark of aging and age-related diseases. Traditionally, the lysosome/vacuole is thought to import free protons (H⁺) from the surrounding neutral cytosol. Here, we uncovered a conserved lysosome/vacuole acidification mechanism from yeast to human involving lysosomal/vacuolar uptake of H+ pumped out by mitochondrial electron transport chain through mitochondria-lysosomes/vacuoles membrane contacts. Aging/senescence-associated disruption of mitochondria-lysosome/vacuole contacts causes lysosomal/vacuolar de-acidification, which can be reversed by either expressing an engineered linker to connect these two organelles or through an asymmetry-dependent rejuvenation process in daughter cells. Preserving lysosomal acidification in senescent human cells prevents the induction of major senescence-associated secretory phenotype factors and restores autophagic flux. These findings reshape our current understanding of the mechanisms underlying lysosomal/vacuolar (de-)acidification in both young and aged/senescent cells.
    Keywords:  Mito-Vac/Lyso contacts; SASP; aging; autophagy; cellular senescence; mitochondria; proton; vacuolar/lysosomal acidification
    DOI:  https://doi.org/10.1016/j.molcel.2026.05.004
  13. Commun Biol. 2026 May 26.
      KRAS inhibitors are reshaping the cancer-treatment landscape; however, durable responses remain limited by drug-tolerant persister cells that survive initial therapy and drive relapse. We show that KRAS-mutant pancreatic and lung cancer cells enter a reversible drug-tolerant (TR) state upon KRAS inhibition, marked by proliferative arrest and extensive metabolic adaptation. Integrated proteomic and metabolomic analyses reveal lysosome-linked remodeling and relatively broad metabolic reprogramming in TR cells. Dual blockade of glutamine metabolism and lysosome-associated processes selectively compromises TR-cell viability under KRAS inhibition, which is rescued by α-ketoglutarate (α-KG). N-acetyl-L-cysteine phenocopies the rescue, and α-KG supplementation lowers intracellular reactive oxygen species levels, supporting a model in which α-KG acts predominantly as a redox-supportive metabolite rather than a Tricarboxylic Acid Cycle intermediate, in the TR state, with lysosome-associated processes contributing to redox balance. These findings define drug-tolerant redox vulnerability and provide a rationale for co-targeting glutamine metabolism and lysosome-associated processes during KRAS inhibitor therapy.
    DOI:  https://doi.org/10.1038/s42003-026-10374-x
  14. Cell Rep. 2026 May 28. pii: S2211-1247(26)00549-8. [Epub ahead of print]45(6): 117471
      Intermuscular fat infiltration driven by fibro-adipogenic progenitors contributes to the irreversible progression of sarcopenia and reflects a fate shift associated with altered calcium signaling. Using FAP-based adipogenesis models, structural and biochemical analyses, transcriptomic profiling, and in vivo drug exposure studies, we found that Ca2+ influx dyshomeostasis promotes adipogenic commitment by triggering calmodulin remodeling, dissociation of the KCNQ1-CaM-FTO complex, nuclear translocation of FTO, and m6A-dependent alternative splicing of RUNX1T1. This cascade reduces the lipogenesis-restrictive RUNX1T1-L isoform and reinforces the C/EBPα-PPARγ positive feedback loop. RUNX1T1-L restoration corrected adipogenesis, stemness, and senescence defects more broadly than FTO inhibition, whereas amlodipine increased mesenteric fat accumulation and was associated with steatotic liver change in mice. These findings link calcium signaling to RNA processing-dependent fate control and highlight potential metabolic liabilities of broad calcium channel blockade.
    Keywords:  CP: Metabolism; CP: Molecular biology; CaM; FAPs; FTO-m6A-RUNX1T1 axis; adipogenesis; calcium channel blockers; calcium signaling
    DOI:  https://doi.org/10.1016/j.celrep.2026.117471
  15. NPJ Aging. 2026 May 26.
      Mitochondrial homeostasis is majorly maintained through mitochondrial autophagy (mitophagy). Recent research highlights the region- and cell type-specific nature of mitophagy during brain aging; however, these dynamics have largely remained unexplored in living brains. To address this gap, we conducted two-photon mt-Keima imaging in somatosensory cortical neurons and astrocytes in behaving male mice across two age groups, including 2-3-month-old (early-aged) and 18-20-month-old (old-aged) mice. We show reduced mitophagy in both cell types during aging, and we consistently found a higher level of mitophagy in astrocytes compared to neurons at the same age, in both age groups. Pharmacological augmentation of NAD+, a pivotal metabolite that induces mitophagy but normally declines in the aging brain, increased cellular mitophagy in both neurons and astrocytes in old-aged male mice at the dose and method of administration tested. Collectively, our data support an age-dependent reduction of mitophagy in neurons and astrocytes, at least in mouse somatosensory cortex, while NAD+ repletion offsets such reduction.
    DOI:  https://doi.org/10.1038/s41514-026-00414-5
  16. Front Immunol. 2026 ;17 1794817
      Succinylation, a dynamic post-translational modification characterized by the addition of a succinyl moiety to lysine residues, has emerged as a pivotal regulator at the interface of metabolic reprogramming and immune surveillance in cancer. This review systematically delineates the molecular mechanisms and therapeutic implications of succinylation in cancer immunotherapy. We detail the writers (e.g., CPT1A, KAT2A), erasers (e.g., SIRT5, SIRT7), and readers that constitute the enzymatic systems governing its dynamics, as well as its profound impact on core metabolic networks including the TCA cycle and glycolysis, thereby fueling tumor progression. Crucially, succinylation has been shown to regulate the tumor immune microenvironment by regulating immune checkpoint stability (e.g., promoting PD-L1 degradation), shaping the polarization and function of macrophages, dendritic cells, and T cells, and influencing immunogenic cell death. These modifications create a complex duality, capable of both enhancing anti-tumor immunity and facilitating immune evasion. We further summarize emerging therapeutic strategies, including small-molecule inhibitors targeting succinylation enzymes, metabolic interventions, and combination therapies designed to harness this pathway to overcome immunotherapy resistance. Finally, we discuss current challenges such as the incomplete mapping of enzyme-substrate relationships and the spatiotemporal heterogeneity of modifications within tumors, while highlighting future directions integrating CRISPR screening, AI prediction models, and single-cell multi-omics to advance precision targeting of succinylation for innovative cancer immunotherapies.
    Keywords:  cancer immunotherapy; metabolic reprogramming; succinylation; targeted therapy; tumor immune microenvironment
    DOI:  https://doi.org/10.3389/fimmu.2026.1794817
  17. bioRxiv. 2026 May 13. pii: 2026.05.11.724378. [Epub ahead of print]
      Astrocytes directly influence neuronal survival and increasingly are understood to contribute to the progression of neurodegenerative diseases including Parkinson's disease (PD). Mitochondrial damage is a hallmark of PD pathology in both neurons and astrocytes. Damaged mitochondria are cleared by PINK1/Parkin-mediated mitophagy; loss-of-function mutations in either PINK1 or Parkin are sufficient to cause PD. Neuronal mitophagy is well-studied, but far less is known about how mitochondrial dysfunction in astrocytes affects neural health. While microglial release of pro-inflammatory cytokines has been shown to induce astrocytes to mount their own inflammatory response, we hypothesize that a more direct pathway is involved, and that mitochondrial damage to astrocytes directly triggers release of proinflammatory cytokines. To address these questions, we treated primary murine cortical astrocytes with oxidative phosphorylation (OXPHOS) inhibitors antimycin A (AA) and oligomycin A (OA) and observed the PINK1-dependent accumulation of Parkin on damaged mitochondria, leading to phospho-ubiquitination of proteins in the outer mitochondrial membrane and the recruitment of the autophagy receptor SQSTM1/p62. To identify transcriptional changes caused by mitochondrial damage and the resulting activation of mitophagic machinery, we performed bulk RNA-sequencing on astrocytes isolated from WT, PINK1 -/- , or Parkin -/- mice treated with AA/OA or a vehicle control. In WT astrocytes, TNF-α signaling via NF-κB was the most significantly upregulated pathway following OXPHOS inhibition. OXPHOS inhibitor treatment also stimulated p62 expression, while NF-κB inhibition prevented this upregulation. Astrocytic secretion of cytokines, including TNF-α, was increased following mitochondrial damage; this secretion was dependent on NF-κB activation and occurred at levels sufficient to induce mitochondrial depolarization in hippocampal neurons. Compared to WT astrocytes, PINK1 -/- astrocytes showed a significant reduction in transcriptional signatures associated with TNF-α signaling following mitochondrial damage, while Parkin -/- astrocytes exhibited upregulation of both IFN-γ and IFN-α signaling. These findings indicate altered inflammatory responses to mitochondrial damage in the absence of functional PINK1 or Parkin. Finally, we analyzed scRNA-sequencing data from substantia nigra astrocytes harvested from human brain tissue from PD-positive or control samples. Distinct clusters comprised predominantly of PD-positive or control astrocytes emerged. Astrocytes in the PD-positive cluster were enriched for NF-κB, IFN-α and IFN-γ responses, consistent with the signaling observed in vitro post-OXPHOS inhibition. Together, these findings identify inflammatory signatures activated by mitochondrial damage in astrocytes, and establish this pathway as a potential contributor to neuroinflammation in PD.
    DOI:  https://doi.org/10.64898/2026.05.11.724378
  18. FEBS J. 2026 May 27.
      For years, the function of Sestrin proteins has been assigned to antioxidant protection and regulation of mTOR complexes 1 and 2. However, recent data demonstrate that Sestrins have a new role in the regulation of mitochondrial functions through incompletely understood mechanisms. These include Sestrin involvement in the control of mitochondrial biogenesis, respiration and mitophagy. Machado et al. describe a key role of Sestrin2 in the regulation of mitochondrial function in myoblast C2C12 cells. Sestrin2 supports mitochondrial biogenesis and respiration through control of mitochondrial protein expression and tuning up mitophagy. These discoveries expand our understanding of the potential role of Sestrins in supporting muscle function through mitochondrial signalling.
    Keywords:  ageing; mTOR; mitochondria; myoblasts; sestrin
    DOI:  https://doi.org/10.1111/febs.70604
  19. FASEB J. 2026 May 31. 40(10): e71953
      Chronic renal failure (CRF) is a growing global health burden, with renal fibrosis representing its key pathological feature. However, the metabolic mechanisms linking mitochondrial dysfunction to redox imbalance during fibrogenesis remain incompletely understood. In this study, we investigated the relationship between mitochondrial oxidative phosphorylation (OXPHOS) disruption and alterations in cellular redox metabolism during CRF progression. Integrated proteomic and metabolomic analyses revealed remodeling of mitochondrial respiratory chain components together with reduced expression of NADPH-generating enzymes, including ME1, ME2, and IDH1. These changes were accompanied by decreased NADPH availability, imbalance of the glutathione redox system (GSH/GSSG), and suppression of NRF2-dependent antioxidant defenses, including HO-1 and GPX4. These alterations were associated with increased oxidative stress and extracellular matrix accumulation in fibrotic kidneys. In vitro experiments further showed that N-acetylcysteine (NAC) partially restored redox homeostasis, improved mitochondrial function, and attenuated TGF-β1-induced profibrotic responses in renal fibroblasts. In addition, the mitochondria-targeted antioxidant Mito-TEMPO reduced mitochondrial ROS accumulation and alleviated fibroblast activation. Collectively, these findings suggest that coordinated disruption of mitochondrial OXPHOS, NADPH metabolism, and glutathione-dependent antioxidant defense is associated with redox imbalance during renal fibrosis. Targeting mitochondrial redox metabolism may therefore represent a potential strategy for mitigating fibrotic progression in CRF.
    Keywords:  NADPH; chronic renal failure; glutathione; mitochondrial dysfunction; oxidative phosphorylation; renal fibrosis
    DOI:  https://doi.org/10.1096/fj.202600552RRR
  20. Cell Rep. 2026 May 28. pii: S2211-1247(26)00452-3. [Epub ahead of print]45(6): 117374
      Understanding how the human brain develops and functions requires direct analysis of human cells. Single-cell atlases open unprecedented opportunities to survey cell physiological molecular states as the brain develops. However, technical challenges limit their potential. We present NeuRoDev, a computational resource with highly curated transcriptomic data and novel analytical tools to investigate neuronal and glial development in the human cortex. NeuRoDev compresses ∼1M single-cell transcriptomes into integrative summary networks of reproducible cell clusters that capture temporal and cellular variation across all stages of human brain development. It provides a reference framework to directly interrogate cellular maturation dynamics, contextualize gene function, and interpret experimental organoid models. We use NeuRoDev to investigate developmental variation in cell physiology, reconstruct genesis and maturation dynamics in neuronal and glial cells, and interpret time-series data from human organoids. NeuRoDev is provided as a freely available software package and web applications for interactive data analysis.
    Keywords:  CP: neuroscience; brain; cortex; development; glia; networks; neurogenesis; neuron; single-cell; transcriptomics
    DOI:  https://doi.org/10.1016/j.celrep.2026.117374