bims-microg Biomed News
on Microglia in health and disease
Issue of 2026–04–05
twenty papers selected by
Marcus Karlstetter, Universität zu Köln



  1. Immunity. 2026 Mar 31. pii: S1074-7613(26)00121-4. [Epub ahead of print]
      Glioblastoma (GB) cells infiltrate the brain parenchyma and colonize distant regions, driving recurrence and therapy resistance. Here, we examined dynamic microglial responses to infiltrating tumor cells during GB progression. Three-photon imaging in an autochthonous, immunocompetent GB mouse model enabled visualization of microglia-GB interactions at the far infiltration zone (FIZ) in the corpus callosum (CC). GB infiltration speed varied by anatomical location and tumor microtube (TM) number. Microglia increased surveillance in sparsely infiltrated areas but reduced it with higher GB density, revealing a biphasic response. Directional migration toward GB cells was restricted to microglial subsets within a defined spatial range, indicating heterogeneous reactivity. CX3CR1 deficiency enhanced microglial reactivity while limiting GB cell migration. Microglia depletion with the CSF1R inhibitor PLX5622 reduced GB cell migration and constrained TM plasticity. Thus, microglia respond to GB cell infiltration in a stage-dependent manner and critically modulate dissemination at the FIZ.
    Keywords:  CSF1R inhibition; CX3CR1-deficiency; Corpus callosum; autochthonous mouse model; diffuse infiltration; glioblastoma; microglia; migration; motility; three-photon microscopy; tumor microtubes
    DOI:  https://doi.org/10.1016/j.immuni.2026.03.010
  2. ACS Nano. 2026 Mar 29.
      Uveitis is a leading cause of vision loss in the working-age population, yet conventional hormone therapy often comes with numerous side effects. Here, we present a noninvasive topical treatment strategy using HSCDs─a bioactive carbon dot derived from plant-based components─as eye drops for autoimmune uveitis. We developed these carbon dots with strong scavenging capacity against reactive oxygen and nitrogen species (RONS) and the ability to penetrate from the ocular surface into the retina. In an experimental autoimmune uveitis (EAU) mouse model, this treatment demonstrated dual-pronged therapeutic effects by alleviating oxidative stress, inhibiting microglial M1 activation via the Nrf2/HO-1 pathway, and reducing the inflammatory reactivity of retinal vascular endothelial cells, while restoring retinal vascular homeostasis, thereby ameliorating uveitis. Additionally, a biosafety assessment confirmed that HSCDs possess favorable biocompatibility and immunological safety. Collectively, our work establishes these carbon dots as a safe and effective topical nanotherapeutic for autoimmune uveitis.
    Keywords:  anti-inflammatory; autoimmune uveitis; carbon dots; microglia; reactive oxygen species; retinal vascular endothelia cells
    DOI:  https://doi.org/10.1021/acsnano.5c20902
  3. Neuron. 2026 Apr 01. pii: S0896-6273(26)00175-3. [Epub ahead of print]
      Recent human genetic studies have highlighted the potential role of microglial genes and their regulatory functions in the pathogenesis of Alzheimer's disease (AD). The transcription factor PU.1 (encoded by SPI1) is expressed mainly in microglia in the central nervous system and has been reported to be a genetic risk factor for AD. However, the role of microglial SPI1 in AD etiology is still poorly understood. Here, we demonstrate that the selective deletion of Spi1 in microglia exacerbates AD-related pathologies in an amyloid mouse model. Specifically, microglial Spi1 deletion increases amyloid deposition, gliosis, and dystrophic neurites while decreasing the microglial response to plaques. By combining proteomics and functional analyses, we reveal that the loss of microglial Spi1 impairs phagocytosis through Syk, Lyn, and Fcgr1. Furthermore, directly activating these genes rescues the impaired amyloid-beta (Aβ) uptake caused by Spi1 knockdown, unveiling the potential mechanism of SPI1 in amyloid pathology.
    Keywords:  Alzheimer’s disease; Fcgr1; Lyn; PU.1; SPI1; Syk; amyloid; amyloidosis; microglia; phagocytosis
    DOI:  https://doi.org/10.1016/j.neuron.2026.03.011
  4. J Clin Invest. 2026 Apr 02. pii: e196112. [Epub ahead of print]
      Traumatic brain injury (TBI) disproportionately affects the elderly, yet the underlying mechanisms remain unclear. Here, we demonstrate that aged TBI brains predominantly harbor pro-inflammatory NLRP3+ microglia, in stark contrast to the neuroprotective Lysozyme+ microglia prevalent in young TBI brains. This age-dependent microglial dichotomy correlates with elevated mortality and impaired recovery in aged TBI mice. By leveraging an integrative multi-omics approach combined with metabolomics and epigenome analysis, we identify a previously unrecognized link between enhanced glycolysis and pro-inflammatory chromatin landscape in NLRP3+ microglia. Further investigation identifies ELF1 as a key transcription factor driving NLRP3+ microglia formation. Importantly, ablation of ELF1 reverses age-associated microglial dysfunction and improves TBI outcomes. Finally, we discover that Imeglimin, a clinically approved antihyperglycemic agent capable of crossing the blood brain barrier, inhibits ELF1 and reverses microglial phenotype, reducing acute mortality rate and leading to improved functional recovery of aged TBI mice. Our work elucidates the mechanistic basis of age-dependent TBI outcomes, reveals the crosstalk between metabolic rewiring and epigenetic regulation in microglial aging, and identifies ELF1 as a promising therapeutic target for improving TBI outcome.
    Keywords:  Drug therapy; Immunology; Inflammation; Innate immunity; Neurodegeneration; Neuroscience
    DOI:  https://doi.org/10.1172/JCI196112
  5. Adv Sci (Weinh). 2026 Mar 31. e04511
      Microglia play a crucial role in the progression of neuroinflammation following traumatic brain injury (TBI). Interleukin-3 (IL-3), a significant regulatory factor, has been involved in the pathogenesis of various diseases, yet its effects on neuroinflammation post-TBI through microglia remain unclear. Here, we evaluate the potential of IL-3 to alleviate neuroinflammation in microglia following TBI. Using the ABplex Multi-Metric Streaming Joint Analysis to detect inflammatory factors, we observed significantly elevated levels of IL-3 in cerebrospinal fluid, but not in blood samples, of patients with headaches and TBI. In addition, we found that administration of exogenous IL-3 within the brain reduced neuroinflammation and promoted functional recovery in rat TBI models. Mechanistically, we identified Peroxiredoxin-1 (PRDX1) as the target of IL-3 in microglia. Notably, the protective effects of IL-3 in TBI rats were abolished when PRDX1 was specifically knocked down in microglia. In conclusion, our experimental research demonstrates that IL-3 acts as a key modulator via regulating microglia polarization to inhibit neuroinflammation. IL-3 improves neurological function and prognosis in TBI rats by recruiting PRDX1 through IL-3R to modulate microglia polarization. Therefore, IL-3 may represent a novel therapeutic strategy for TBI.
    Keywords:  IL‐3; PRDX1; astrocytes; microglia; traumatic brain injury
    DOI:  https://doi.org/10.1002/advs.202504511
  6. Alzheimers Dement. 2026 Apr;22(4): e71336
       INTRODUCTION: Cerebral small vessel disease (CSVD) is the most prevalent pathology underlying vascular dementia. Increased neuroinflammation and blood-brain barrier (BBB) permeability have been implicated in CSVD pathogenesis. We determined whether microglial reactivity and BBB permeability at baseline predicted whole-brain and hippocampal atrophy over one year, and cognitive impairment over four years.
    METHODS: Seventy-seven patients with CSVD were recruited to this prospective study. Baseline microglial reactivity and BBB permeability were determined using 11C-PK11195 positron emission tomography and dynamic contrast enhanced (DCE) MRI respectively.
    RESULTS: Greater 11C-PK11195 binding at baseline was associated with hippocampal atrophy over one year (p = 0.001), but not with global brain atrophy. Cox regression analyses showed no significant associations between 11C-PK11195 and cognitive impairment. There were no associations between BBB permeability with whole-brain and hippocampal atrophy, or with cognitive impairment.
    DISCUSSION: Our data suggests that microglial reactivity may play a role in hippocampal atrophy; potentially contributing to the increasingly recognized interaction between vascular and neurodegenerative pathology.
    Keywords:  MRI; blood‐brain barrier; dementia; neuroinflammation; positron emission tomography; stroke; vascular cognitive impairment
    DOI:  https://doi.org/10.1002/alz.71336
  7. Proc Natl Acad Sci U S A. 2026 Apr 07. 123(14): e2527009123
      Traumatic brain injury (TBI) is a leading cause of morbidity and mortality, with closed-head mild TBI (mTBI) accounting for nearly 90% of all cases. Early pathological events include microglial activation and neuronal mitochondrial dysfunction; however, their interconnection in mTBI remains poorly understood. Using a clinically relevant closed-head weight-drop mouse model, we identified mitochondrial DNA (mtDNA)-specific damage and increased expression of innate inflammatory markers (IL-1α/β, IL-6, TNFα, and CXCL1) in the cerebral cortex during the acute mTBI phase. Mechanistically, neurons subjected to in vitro injury model of mTBI exhibited early mtDNA-specific damage followed by mtDNA release via extracellular vesicles (EVs) together with the neuronal and exosomal markers. The released neuronal mtDNA induced a robust microglial activation mediated by binding to the cytoplasmic DNA/RNA sensor Z-DNA-binding protein 1 (ZBP1), triggering activation of the ZBP1-TBK1-IRF3 pathway resulted IL-6 and TNFα expression. An early, enhanced amounts of mtDNA, neuronal and exosomal markers were measured in EVs circulating in the blood of mice subjected to mTBI. ZBP1 knockout (KO) mice displayed suppressed microglial-but not astrocytic-activation in the cortex during the acute mTBI phase. We also measured accumulation of mtDNA-specific damage in the hippocampus during the postacute mTBI phase. The absence of microglial activation in ZBP1 KO mice exacerbated hippocampal-related memory deficits in the postacute mTBI phase. Collectively, our findings identify mtDNA-ZBP1 signaling as a key mechanism regulating microglial activation in mTBI.
    Keywords:  Z DNA binding protein 1; microglia; mild traumatic brain injury; mitochondrial DNA; neuroinflammation
    DOI:  https://doi.org/10.1073/pnas.2527009123
  8. Mol Psychiatry. 2026 Apr 01.
      Microglia-neuron contacts have been shown to regulate neural network activity through the formation and elimination of synapses. The pathogenesis of major depressive disorder is accompanied by a decline in brain-derived neurotrophic factor (BDNF) signaling, associated with increased microglia activity that disrupts cognitive function. The actions of both typical and rapid-acting antidepressant drugs, which have been shown to increase BDNF signaling through the tropomyosin receptor kinase B (TrkB) receptor, decrease microglia activation and the levels of pro-inflammatory cytokines. Examining the link between BDNF signaling and the microglial pro-inflammatory response, we demonstrate that TrkB signaling elicits the neuronal secretion of CD22 (Siglec-2), a sialic acid-binding immunoglobulin-type lectin, to inhibit microglial activation and alleviate depression-like symptoms. In a male chronic mild stress (CMS) mouse model of depression decreased expression of the postsynaptic scaffolding protein PSD-95 and Gαi1/3 were found to compromise TrkB signaling leading to reduced CD22 levels in hippocampal tissue. Restoration of TrkB-Gαi1/3-Akt signaling with dSyn3, a peptidomimetic compound targeting the PDZ3 domain of PSD-95, enhanced CD22 expression to inhibit microglial activation, promote dendritic spine formation and rapidly mitigate depression-like symptoms. Furthermore, hippocampal overexpression of CD22 in neurons was sufficient to reduce microglial activation and depressive-like behaviors in male CMS mice. S-ketamine, a rapid-acting antidepressant, increased CD22 expression to mitigate depression-like symptoms. While neuronal knockdown of CD22 in the hippocampus did not significantly impair the rapid (within 4 h) antidepressant effects typically observed with S-ketamine or dSyn3 administration, strikingly, knockdown of CD22 attenuated the long-acting (within 3 days) antidepressant effects of S-ketamine or dSyn3, as evidenced by sustained immobility in the TST (tail suspension test) and FST (forced swim test), and a lack of improvement in sucrose preference. In contrast, a single dose of fluoxetine failed to increase CD22 expression or inhibit microglia activity. These results suggest that rapidly-acting anti-depressant drugs enhance TrkB-induced neuronal expression and secretion of CD22 to promote the homeostatic state of microglia required for antidepressant actions. In male depression mice, dSyn3 facilitates BDNF-induced TrkB-PSD-95-Gαi1/3 complex formation to increase Akt-mTOR activation as well as synaptic and spine density in the hippocampus. TrkB signaling increases CD22 expression and secretion from neurons blocking microglial activation in the hippocampal region of male CMS mice.
    DOI:  https://doi.org/10.1038/s41380-026-03575-7
  9. Cell Death Discov. 2026 Mar 31.
      Patients with neurodegenerative diseases such as retinitis pigmentosa (RP) may engage in maladaptive coping behaviors, including alcohol misuse, which can aggravate disease progression. Neuroinflammation, a hallmark of RP, is largely driven by microglial activation and amplified when cells are primed by oxidative stress. Store-operated calcium entry (SOCE), primarily mediated by Orai1 channels, regulates microglial metabolism and inflammatory signaling. Here, we tested whether ethanol (EtOH) exacerbates RP-related neuroinflammation through SOCE-dependent mechanisms and whether 2-aminoethoxydiphenyl borate (2-APB) mitigates these effects. In mixed retinal cultures, a "double-hit" (oxidative stress + EtOH) triggered pronounced microglial activation, neuronal loss, and altered cytokine expression and correlation patterns, assessed by multiplex bead assays and hierarchical clustering analysis. Indeed, 2-APB restored ramified morphology and improved neuronal survival. Conditioned medium experiments revealed that both microglia and Müller cells responded to the double-hit, but only microglia were sensitive to SOCE inhibition. In vivo, subretinal delivery of EtOH and 2-APB in rd1 mice, a genetic model of RP, altered microglial morphology and reduced pro-inflammatory cytokine levels without affecting photoreceptor density. Notably, in situ assessment of CD86/CD206 showed no change in expression, indicating that microglial activation in vivo is better captured by morphological and cytokine-network alterations than by classical surface markers. These findings show that alcohol misuse amplifies retinal neuroinflammation in RP via calcium-dependent mechanisms and identify SOCE as a therapeutic target for limiting damage from systemic comorbidities in retinal degeneration.
    DOI:  https://doi.org/10.1038/s41420-026-03074-2
  10. JCI Insight. 2026 Apr 02. pii: e201466. [Epub ahead of print]
      Huntington's disease (HD) is a fatal neurodegenerative disease caused by an expanded polyglutamine (CAG) repeat in the N-terminal of the Huntingtin protein (HTT). Microglial activation and elevated pro-inflammatory cytokines are observed in HD brains, but the mechanisms regulating neuroinflammation and microglial activation are poorly understood. Metformin-mediated neuroprotection has been demonstrated in experimental models of neurodegeneration, including HD. We found that metformin inhibits mitochondrial DNA (mtDNA) release and subsequent neuroinflammation in the cortex and striatum of a mouse model of HD. Moreover, elevated pro-inflammatory cytokines and microglial activation are inhibited by metformin in HD transgenic mice brain. Metformin reduced pathological microglial clusters and shifted towards a quiescent, homeostatic phenotype. Metformin improved aberrant immunometabolism in HD mouse brain and primary microglia. Mechanistically found that metformin regulates mitochondrial fission, reprograms deregulated metabolism in HD microglia, and controls microglial activation and inflammation in HD transgenic mice.
    Keywords:  Glucose metabolism; Metabolism; Neurodegeneration; Neuroscience
    DOI:  https://doi.org/10.1172/jci.insight.201466
  11. Cell Rep. 2026 Mar 27. pii: S2211-1247(26)00228-7. [Epub ahead of print]45(4): 117150
      Directed migration and rapid process extension-retraction allow microglia to continuously survey the brain and efficiently identify and phagocytose apoptotic neurons. Defining how cytoskeletal regulators coordinate these behaviors could guide strategies for targeted modulation of microglial activity. To this aim, using in vivo imaging in zebrafish, we identified a mechanistic framework in which myosin II-dependent contractility governs transitions between surveillance, migratory, and phagocytic states. Building on this, we engineered an optogenetic RhoA actuator (opto-ArhGEF25) that enables reversible, spatiotemporally precise manipulation of microglial behavior in vivo. We show that patterned RhoA activation can modulate process dynamics and induce front-rear polarity that drives rapid repulsive migration away from the applied light source, overriding injury-evoked cues and preventing migration toward lesions. Together, these results establish optogenetic control of the cytoskeleton as a powerful approach to probe and ultimately modulate microglial function in the living brain.
    Keywords:  CP: cell biology; CP: neuroscience; Myosin; RhoA; branching dynamics; cell migration; cell polarity; efferocytosis; microglia; microscopy; optogenetics; phagocytosis; zebrafish
    DOI:  https://doi.org/10.1016/j.celrep.2026.117150
  12. Cell Rep. 2026 Mar 27. pii: S2211-1247(26)00239-1. [Epub ahead of print]45(4): 117161
      High-expression variants of the complement C4 gene increase schizophrenia (SZ) risk. C4 overexpression (C4-OE) in the mouse frontal cortex recapitulates SZ-associated phenotypes, including lower synapse density, but the underlying mechanisms remain unclear. In the complement cascade, C4 is upstream of C3, whose cleavage fragments can bind complement receptors, including CR3, selectively expressed by microglia in the brain parenchyma. Therefore, we hypothesize that microglial CR3 mediates C4-OE effects. We show that C4-OE alters synapse density and function and that these effects are rescued in CR3-deficient mice. Contrary to the models of excessive microglia-mediated synaptic elimination, our previous results indicate that C4-OE reduces spine formation and elimination. Here, using in vivo two-photon imaging, we find that C4-OE decreases microglial surveilled volume, motility, and the frequency of microglial contacts with pre- and postsynaptic structures. These changes are abolished by CR3 deficiency. Our findings suggest that CR3-mediated modulation of microglia-synapse interactions underlies C4-OE effects relevant to SZ.
    Keywords:  CP: neuroscience; complement; in vivo two-photon; microglia; microscopy; mouse cortex; schizophrenia; synapse; synaptic pruning; synaptic refinement; synaptic remodeling
    DOI:  https://doi.org/10.1016/j.celrep.2026.117161
  13. NPJ Parkinsons Dis. 2026 Mar 28.
      O-GlcNAcylation, a nutrient-sensitive post-translational modification, has emerged as a key regulator of immune and inflammatory processes. However, its role in neuroinflammation and neurodegenerative disease progression remains poorly defined. In this study, we explored how reduced O-GlcNAcylation contributes to neuroinflammatory signaling in Parkinson's disease (PD), a disorder increasingly recognized to involve dysregulated immune-metabolic interactions. Analysis of postmortem PD substantia nigra (SN) revealed a marked reduction in global O-GlcNAcylation levels, concomitant with enhanced neuroinflammatory signatures and a predominance of pro-inflammatory microglial activation states. In a lipopolysaccharide (LPS)-induced PD mouse model, pharmacological elevation of O-GlcNAcylation through glucosamine (GlcN) or the Thiamet-G significantly ameliorated motor deficits, preserved tyrosine hydroxylase (TH)-positive dopaminergic neurons, and attenuated neuroinflammatory responses, including glial activation and inflammasome assembly. In primary microglial cultures, enhanced O-GlcNAcylation suppressed LPS-induced pro-inflammatory gene expression while promoting anti-inflammatory and homeostatic phenotypes. Mechanistically, increased O-GlcNAcylation dampened NF-κB signaling activity and reduced the production of pro-inflammatory cytokines, thereby reprogramming microglial functional states. Collectively, these findings identify O-GlcNAcylation as a critical modulator of microglial-mediated neuroinflammation and highlight its therapeutic potential for inflammation-associated neurodegenerative disorders such as PD.
    DOI:  https://doi.org/10.1038/s41531-026-01319-6
  14. Aging Cell. 2026 Apr;25(4): e70458
      Postoperative delirium (POD) accelerates the transition from mild cognitive impairment (MCI) to Alzheimer's disease (AD) in elderly patients. Microglial metabolic reprogramming, a pivotal aspect of the immune-inflammatory response, modulates microglia-neuron interactions and postoperative cognitive function through microenvironmental alterations. Aberrant overexpression of RUVBL2 disrupts metabolic homeostasis, leading to stress granule (SG) aggregation and fibrosis. This study investigated the role of RUVBL2 in regulating metabolic reprogramming to mediate SG formation, with the aim of identifying novel prognostic targets for inhibiting glycolysis and mitigating POD-induced MCI progression. A POD model was established in aged MCI rats using 3% sevoflurane anesthesia for 3 h, combined with open reduction and internal fixation (ORIF). Multimodal magnetic resonance imaging (MRI) was employed to assess postoperative cognitive function. Glycolytic and oxidative phosphorylation (OXPHOS) activities in primary hippocampal microglia were quantified by extracellular acidification rate (ECAR) and oxygen consumption rate (OCR). Lentiviral-mediated RUVBL2 expression modulation was performed to verify its role in microglial metabolic reprogramming. Postoperative hippocampal microglia underwent metabolic reprogramming from OXPHOS to glycolysis, with RUVBL2 expression correlating positively with POD progression. Elevated RUVBL2 expression drove metabolic reprogramming, while RUVBL2 knockdown inhibited this process, alleviated pro-inflammatory microglia-induced neuroinflammation and SG aggregation, and improved spontaneous neural activity and hippocampus-dependent cognitive deficits. In primary hippocampal microglia, RUVBL2 knockdown enhanced OXPHOS-related OCR and reduced glycolysis-associated ECAR, producing a synergistic neuroprotective effect. These findings reveal the critical role of RUVBL2 in regulating POD, highlight metabolic reprogramming as a novel therapeutic target, and suggest RUVBL2 as a promising intervention strategy for POD.
    Keywords:  RUVBL2; metabolic reprogramming; microglia; neuroinflammation; postoperative delirium (POD); stress granules (SGs)
    DOI:  https://doi.org/10.1111/acel.70458
  15. Front Immunol. 2026 ;17 1731962
      Itaconate is produced by inflammatory macrophages and promotes negative feedback on inflammation. It is synthesized by aconitate decarboxylase 1 (ACOD1) from cis-aconitate, a metabolite of the tricarboxylic acid cycle. Here, we focused on the role of ACOD1 in the immunometabolic reprograming of inflammatory microglia. Similar to macrophages, ACOD1 deficient microglia displayed a stronger inflammatory response to lipopolysaccharide (LPS) compared to their wild type counterparts. The proinflammatory effects of ACOD1 deficiency were associated with enhanced ATP citrate lyase (ACLY) activity and elevated acetyl-CoA amounts, and reprogramed arginine metabolism entailing enhanced argininosuccinate synthesis at the expense of polyamine biosynthesis. These effects of ACOD1 deficiency on arginine metabolism were reversed by ACLY inhibition. These findings provide new insights in the immunometabolic role of ACOD1.
    Keywords:  ACLY; ACOD1; argininosuccinate; microglia; polyamines
    DOI:  https://doi.org/10.3389/fimmu.2026.1731962
  16. Neurotherapeutics. 2026 Mar;pii: S1878-7479(26)00061-9. [Epub ahead of print]23(2): e00891
      
    Keywords:  Epigenetic regulation; Glial scar; Innovative therapy; Lipid metabolism; Microglia; Spinal cord injury
    DOI:  https://doi.org/10.1016/j.neurot.2026.e00891
  17. Behav Brain Res. 2026 Mar 28. pii: S0166-4328(26)00170-1. [Epub ahead of print]507 116194
      Social animals are faced with a critical decision when sick: to affiliate or withdraw. The behavioural response during an immune challenge varies by individual and species. However, the social and biological factors leading to variation in this decision during an immune challenge are unknown. Here, we explore the affiliative behavioural phenotype, "huddlers" and "non-huddlers," as a social predictor, and microglial activation and peripheral cytokine expression as biological predictors of social decision-making during an immune challenge. To measure social decision-making, we recorded social approach and time spent in proximity to a familiar same-sex conspecific versus a novel object in the social California mouse following lipopolysaccharide (LPS) treatment. Behavioural phenotype predicted both the social response to LPS and the relationship between cytokine activity and social behaviour, suggesting that social experience regulates social decision-making during sick versus healthy conditions. Additionally, we found that elevated microglia activity in the dentate gyrus (DG) and medial prefrontal cortex (mPFC) negatively correlated with social behaviour, positioning these regions for future exploration for the role of microglia on social decision-making. Our results identify the predictive power of behavioural phenotypes on social response to sickness and a link between microglia and decision-making during sickness.
    Keywords:  Affiliation; Inflammation; Lipopolysaccharide; Microglia; Prefrontal cortex; Social decision-making; Ultrasonic vocalizations
    DOI:  https://doi.org/10.1016/j.bbr.2026.116194
  18. Behav Brain Res. 2026 Mar 28. pii: S0166-4328(26)00163-4. [Epub ahead of print]507 116187
      Central post-stroke pain (CPSP) is a neuropathic pain condition that severely impairs patients' quality of life and recovery, yet its pathogenesis remains poorly understood. This study employed a multi-omics approach to investigate CPSP mechanisms in a mouse model generated by stereotaxic injection of collagenase IV into the thalamic ventral posterolateral nucleus (VPL). Pain-related behavioral tests confirmed successful model establishment and characterized associated behavioral deficits. Subsequent analyses using ELISA, qPCR, and immunofluorescence revealed elevated inflammatory cytokine levels and microglial activation in the VPL. Non-targeted metabolomics and transcriptomics further uncovered significant metabolic and gene expression changes in CPSP mice. Integrated multi-omics analysis identified the kinase Lyn as a key differentially expressed gene linked to these metabolic alterations, with its expression dynamically upregulated in CPSP mice. Lyn colocalized with activated microglia and promoted their shift toward a pro-inflammatory phenotype. Importantly, pharmacological inhibition of Lyn using Bafetinib attenuated pain hypersensitivity, suppressed microglial proliferation, and reduced inflammatory cytokine secretion in CPSP mice. These findings indicate that CPSP involves systemic metabolic and transcriptional dysregulation, and that Lyn-mediated microglial activation drives pain progression through enhanced neuroinflammation, highlighting Lyn as a potential therapeutic target for CPSP intervention.
    Keywords:  Central post-stroke pain; Lyn; Metabolism; Microglia; Neuroinflammation
    DOI:  https://doi.org/10.1016/j.bbr.2026.116187