bims-micgli Biomed News
on Microglia
Issue of 2026–04–26
35 papers selected by
Matheus Garcia Fragas, Universidade de São Paulo



  1. Nat Commun. 2026 Apr 23. pii: 3737. [Epub ahead of print]17(1):
      Amyloid beta (Aβ) plaque deposition in the central nervous system (CNS) is a hallmark of Alzheimer's disease (AD) and cerebral amyloid angiopathy (CAA), triggering robust innate immune responses. However, the role of the adaptive immune system remains less well understood. Here we show the immune microenvironment dynamics in APP23 transgenic (APP23-tg) mice modelling CNS amyloid pathology, using single-cell transcriptomics. We observed a marked increase in T-cell populations during late disease stages, particularly CD8⁺ T-cells that clustered around Aβ plaques, suggesting a targeted immune response. Among these, we identified an Aβ plaque-associated subset of CD8⁺ T cells expressing interferon-stimulated genes (ISGs), which promoted Type-I interferon signaling. This subset also produced CXCL10, facilitating the recruitment of non-ISG T cells through the CXCL10-CXCR3 axis. Importantly, similar Type-I interferon responses were detected near plaques in human CNS amyloid pathology. Together, these findings highlight a shift from microglia-driven to T-cell-mediated neuroinflammation as amyloid pathology progresses, with implications for time-resolved therapy development.
    DOI:  https://doi.org/10.1038/s41467-026-72262-6
  2. J Neuroinflammation. 2026 Apr 22.
      
    Keywords:   INPP5D/SHIP1; Alzheimer's disease; Inflammasome; Lipid metabolism; Microglia; Neuroinflammation
    DOI:  https://doi.org/10.1186/s12974-026-03819-x
  3. Nat Commun. 2026 Apr 21.
    Jigyasha Timsina, Chenyang Jiang, Daniel L McCartney, Feifei Tao, Maria Carolina Dalmasso, Jenna Najar, Federica Anastasi, Olena Ohlei, Raquel Puerta Fuentes, Chenyu Yang, Joseph Bradley, Daniel Western, Muhammad Ali, Ciyang Wang, Chengran Yang, Ying Wu, Menghan Liu, John Budde, Julie Williams, Rebecca Mahoney, Atahualpa Castillo Morales, Timothy J Hohman, Logan Dumitrescu, Ting-Chen Wang, Niccolo' Tesi, Silke Kern, Margda Waern, Ingmar Skoog, Argonde van Harten, Yolande A L Pijnenburg, Wiesje M van der Flier, Pascual Sánchez-Juan, Eloy Rodriguez-Rodriguez, Luca Kleineidam, Oliver Peters, Anja Schneider, Fahri Küçükali, Céline Bellenguez, Benjamin Grenier-Boley, Sami Heikkinen, Itziar de Rojas, Dan Rujescu, Norbert Scherbaum, Lucrezia Hausner, Emrah Düzel, Timo Grimmer, Jens Wiltfang, Rik Vandenberghe, Sebastiaan Engelborghs, Stefanie Heilmann-Heimbach, Matthias Schmid, Thomas Tegos, Nikolaos Scarmeas, Oriol Dols-Icardo, Fermin Moreno, Jordi Pérez-Tur, María J Bullido, Raquel Sánchez-Valle, Victoria Álvarez, Pablo García-González, Pablo Mir, Luis M Real, Gerard Piñol-Ripoll, Jose María García-Alberca, Harro Seelaar, Inez Ramakers, Janne Papma, Marc Hulsman, Christoph Laske, Stefan Teipel, Josef Priller, Robert Perneczky, Katharina Buerger, Markus M Nöthen, Piotr Lewczuk, Johannes Kornhuber, Harald Hampel, Ina Giegling, Oliver Goldhardt, Janine Diehl-Schmid, Victor Andrade, Michael Mt Heneka, Lutz Frölich, Jonathan Vogelgsang, Caroline Graff, Hakan Thonberg, Abbe Ullgren, Goran Papenberg, Jean-François Deleuze, Carole Dufouil, Michael Wagner, Frank Jessen, Henne Holstege, Cornelia van Duijn, Thibaud Lebouvier, Olivier Hannon, Ville Leinonen, Hilkka Soininen, Sanna-Kaisa Herukka, Vilmantas Giedraitis, Malin Löwenmark, Lena Kilander, Patricia Genius, Blanca Rodríguez, Emma S Luckett, Arcadi Navarro, Amanda Cano, Marta Marquié, Kaj Blennow, Henrik Zetterberg, Alberto Lleo, Mercè Boada, Agustin Ruiz, Virginia Man-Yee Lee, Vivianna M Van Deerlin, Yuetiva Deming, Sterling C Johnson, Corinne D Engelman, Pau Pastor, Ignacio Alvarez, Elaine R Peskind, Amanda J Heslegrave, Andrew J Saykin, Kwangsik Nho, Suzanne E Schindler, John C Morris, David M Holtzman, Eric McDade, Alan E Renton, Alison Goate, Laura Ibanez, Matthias Riemenschneider, Marilyn S Albert, Simon M Laws, Tenielle Porter, Eleanor K O'Brien, Leslie M Shaw, Betty M Tijms, Martin Ingelsson, Pieter Jelle Visser, Mikko Hiltunen, Kristel Sleegers, Craig W Ritchie, Rebecca Sims, Michael Belloy, Jean-Charles Lambert, Natalia Vilor-Tejedor, Maria Victoria Fernández, Qingqin S Li, Michael W Nagle, Riccardo E Marioni, Alfredo Ramirez, Lars Bertram, Sven J van der Lee, Carlos Cruchaga.
      Cerebrospinal fluid amyloid beta 42, total tau, and phosphorylated tau 181 are well accepted markers of Alzheimer's disease. These biomarkers better reflect disease pathogenesis compared to clinical diagnosis. Here, we perform a genome wide association study meta-analysis including 18,948 individuals of European ancestry and identify 12 genome-wide significant loci across all three biomarkers, eight of them novel. We replicate the association of biomarkers with APOE, CR1, GMNC/CCDC50 and C16orf95/MAP1LC3B. Novel loci include BIN1 for amyloid beta and GNA12, MS4A6A, SLCO1A2 with both total tau and phosphorylated tau 181, as well as additional loci on chr. 8, near ANGPT1 and chr. 9 near SMARCA2. We also demonstrate that these variants have significant association with Alzheimer's disease risk, disease progression and/or brain amyloidosis. The associated genes are implicated in lipid metabolism independent of APOE, coupled with autophagy and brain volume regulation driven by total tau and phosphorylated tau 181 dysregulation.
    DOI:  https://doi.org/10.1038/s41467-026-71682-8
  4. Neuroscience. 2026 May 25. pii: S0306-4522(26)00178-8. [Epub ahead of print]603 290-293
      MeSH terms: Microglia/growth & development; Induced Pluripotent Stem Cells /differentiation; Organoids/physiology; Epigenomics; Cell Lineage.
    Keywords:  Brain organoids; Epigenetic landscape; Microglial maturation; Single-cell RNA sequencing; iPSC-derived microglia
    DOI:  https://doi.org/10.1016/j.neuroscience.2026.03.015
  5. Mol Neurobiol. 2026 Apr 24. pii: 584. [Epub ahead of print]63(1):
      Cognitive impairment (CI), spanning mild memory issues to severe dementia, impacts over 55 million people worldwide and have a significant effect that strains health, economy, and caregiving. Surprisingly, it occurs at any age. The glial cell ecosystem, particularly astrocyte-microglia crosstalk, is pivotal for brain homeostasis and cognitive function across the lifespan. Intriguingly, in recent discoveries, dysregulation of ecosystem contributes to neurodevelopmental disorders (NDDs), adult cognitive decline, and neurodegenerative diseases like Alzheimer's disease (AD), and astrocyte-derived interleukin-3 (IL-3), acting via the IL-3/CD123-related signals, may act as a key regulatory mediator of microglial function. Over the past few decades, extensive researches have been devoted to investigating aging-related regulatory factors with the aim of deciphering the "code" underlying cognitive developmental abnormalities, premature cognitive decline, and neurodegeneration. Astrocyte-microglia crosstalk governs age-dependent glial turnover via senescence-sensitive IL-3. Under pathological conditions, perturbed turnover's association with age-stratified CI and its regulators is poorly understood. This review integrates current evidence on glial crosstalk, cellular senescence, and repopulation to elucidate age-specific CI driven by dysregulated glial turnover, while identifying key biomarkers that can predict aging processes. Looking ahead, therapeutic strategies targeting the IL-3/CD123-related signals regulating glial crosstalk hold promise for advancing interventions in immune-mediated CI across the lifespan.
    Keywords:  Astrocyte-microglia crosstalk; Cell transplantation; Cognitive impairment; Glial cell ecosystem; Interleukin-3; Neurodegenerative diseases
    DOI:  https://doi.org/10.1007/s12035-026-05815-x
  6. Cell Rep. 2026 Apr 22. pii: S2211-1247(26)00381-5. [Epub ahead of print]45(5): 117303
      Aging strongly impacts CD8+ T cells, including the loss of naive cells and the emergence of age-associated GZMK+CD8+ T cells (TAA cells). Although TAA cells constitute a major population in aged mice, the pathway underlying their differentiation remains unknown. Here, we demonstrate that TAA cell development is cell extrinsic and requires antigen exposure within aged non-lymphoid tissues. Using a TNFΔ69AU/+ mouse model, we show that low-grade inflammation accelerates CD8+ T cell aging and promotes early accumulation of TAA cells. Analysis of TAA cell heterogeneity further identifies a progenitor subpopulation enriched in the aged adipose tissue. Finally, heterochronic transplantation experiments suggest that the aged adipose tissue can serve as a systemic source of TAA cells and contribute to the conversion of young CD8+ T cells into the aged phenotype. Together, these findings indicate that aged non-lymphoid tissues actively drive CD8+ T cell remodeling and identify adipose tissue as an important niche shaping immune aging.
    Keywords:  CD8(+) T cells; CP: immunology; adipose tissue; aging; granzyme K; inflammaging
    DOI:  https://doi.org/10.1016/j.celrep.2026.117303
  7. Brain Behav Immun. 2026 Apr 19. pii: S0889-1591(26)00519-2. [Epub ahead of print]136 106771
      Microglia critically influence multiple sclerosis (MS) pathophysiology through debris clearance, myelin repair, and modulation of neuroinflammation. These processes are partly regulated by ATP-gated ion channel P2X4, predominantly expressed in microglia. We previously reported that ivermectin (IVM), a positive allosteric modulator of P2X4, modulates microglia activation and function in myelin phagocytosis and promotes following lysolecithin-induced demyelination, and ameliorates neurological symptoms in experimental autoimmune encephalomyelitis (EAE). Here, we dissected the molecular and cellular basis of this protective effect using P2X4mCherryIN knock-in (P2X4KI) mice, in which P2X4 is replaced by a non-internalized variant (P2X4KI), leading to increased surface localization at the plasma membrane. Indeed, ATP-evoked currents were increased in P2X4KI microglia. Transcriptomic analyses revealed that P2X4KI microglia exhibit suppressed inflammatory and immune signaling pathways, suggesting that P2X4 orchestrates microglial responses to injury. Both constitutive and myeloid-specific P2X4KI mice showed a significant amelioration of EAE motor deficits, although exclusively in females. Notably, ovariectomy abolished P2X4-mediated protection in females whereas administration of progesterone gave protection to P2X4KI males, confirming the requirement of female hormones for P2X4-mediated protection. Indeed, progesterone potentiated P2X4 currents and prolonged channel deactivation, revealing direct hormonal modulation of P2X4 gating. These findings identify P2X4 as a key regulator of neuroinflammatory outcomes and reveal a previously unrecognized interaction between female hormones and P2X4 that underlies sex-specific disease modulation. Targeting this pathway may enable the development of precision therapies for MS.
    Keywords:  EAE; Microglia; Multiple sclerosis; P2X4 receptor; Sex dimorphism
    DOI:  https://doi.org/10.1016/j.bbi.2026.106771
  8. J Neuroinflammation. 2026 Apr 23.
      
    Keywords:  Cholesterol reprogramming; HSP90; High-altitude cognitive impairment; Lipid droplets; Microglia; NRF1; Neuroinflammation; SREBP2; Synaptic pruning
    DOI:  https://doi.org/10.1186/s12974-026-03830-2
  9. J Neuroinflammation. 2026 Apr 23.
      
    Keywords:  Alzheimer’s disease; Interferon-stimulated genes; Microglia; Neuroinflammation; Type-1 interferons
    DOI:  https://doi.org/10.1186/s12974-026-03828-w
  10. Alzheimers Res Ther. 2026 Apr 24. pii: 93. [Epub ahead of print]18(1):
    DELCODE study group
      
    Keywords:  APOE ε4 genotype; Alzheimer’s disease (AD); Biomarkers; Healthy aging; Prevention; Sex differences; Structural equation modeling
    DOI:  https://doi.org/10.1186/s13195-026-02054-z
  11. Proc Natl Acad Sci U S A. 2026 Apr 28. 123(17): e2535044123
      In the zebrafish retina, Müller glia (MG) respond to retinal injury by dividing and producing a multipotent progenitor for retinal repair. This cell division is regulated by microglia; however, the underlying mechanism remains unknown. Here, we report that MG-derived Il34 attracts microglia to sites of retinal injury where they stimulate MG proliferation via the release of cytokines, like M17, Spp1, Tnfa, and Tnfb. Remarkably, RNA sequencing analysis of MG's regeneration-associated transcriptome with and without microglia depletion suggests microglia stimulate MG proliferation by preferentially enhancing the expression of regeneration-associated genes involved in cell division-related processes. In contrast, genetic ablation of essentially all microglia from early development appears to reprogram MG, so they exhibit enhanced injury-dependent proliferation, but their survival is compromised. Our studies illustrate the profound effects MG-microglia cross talk can have on MG transcriptional programs related to cell division processes.
    Keywords:  Müller glia; microglia; regeneration; retina; stem cell
    DOI:  https://doi.org/10.1073/pnas.2535044123
  12. Ageing Res Rev. 2026 Apr 22. pii: S1568-1637(26)00130-3. [Epub ahead of print] 103138
      Microglia, the brain's innate immune cells, undergo a complex activation process characterized by metabolic reprogramming and inflammatory signalling that transcends the classical M1/M2 polarization framework. Recent advances in single-cell technologies have unveiled remarkable microglial heterogeneity, including the emergence of disease-associated microglia (DAM), which play critical roles in neurodegeneration. This study synthesizes recent findings from single-cell transcriptomics, spatial proteomics, and metabolomics to provide an integrated perspective on microglial activation. We focus on the interplay between key metabolic pathways, including glycolysis, the pentose phosphate pathway, and oxidative phosphorylation, as well as inflammatory signalling networks such as NF-κB, HIF-1α, and JAK/STAT, across diverse neurodegenerative conditions. Our synthesis reveals that microglial activation is driven by coordinated metabolic and inflammatory reprogramming, forming self-reinforcing cycles that sustain neuroinflammation. Disease-associated microglia display unique transcriptional profiles distinct from traditional polarization states, with notable regional and sex-specific variations in activation patterns. Crucially, crosstalk between the HIF-1α and NF-κB pathways modulated by metabolic sensors like CARKL underpins persistent inflammatory responses. Additionally, researchers have identified novel neuroprotective mechanisms, including mitochondrial transfer from microglia to neurons via tunnelling nanotubes. Importantly, chronic neuroinflammation in neurodegenerative diseases appears to arise not from persistent microglial activation per se, but from failures in inflammatory resolution. Viewing microglial activation as an integrated metabolic-inflammatory network highlights new therapeutic avenues. While metabolic inhibitors hold conceptual promise, their clinical infeasibility necessitates a paradigm shift toward TREM2 immunomodulators and resolution agonists with established human safety profiles. Strategies targeting metabolic reprogramming, enhancing resolution pathways, and promoting beneficial microglial-neuronal interactions hold promise for treating neurodegenerative disorders. Furthermore, identifying biomarkers of microglial activation states may enable the development of personalized therapeutic approaches.
    Keywords:  Disease-Associated Microglia (DAM); Metabolic Reprogramming; Microglia; Neurodegeneration; Neuroinflammation
    DOI:  https://doi.org/10.1016/j.arr.2026.103138
  13. J Neuroinflammation. 2026 Apr 21. pii: 137. [Epub ahead of print]23(1):
      
    Keywords:  Adaptive immunity; Antiviral immunity; Herpes Simplex Virus (HSV); Infection; Inflammation; Influenza A Virus (IAV); Innate immunity; Lymphocytic Choriomeningitis Virus (LCMV); Neuro-immunology; Nociceptor neurons
    DOI:  https://doi.org/10.1186/s12974-026-03817-z
  14. Brain Behav Immun. 2026 Apr 19. pii: S0889-1591(26)00518-0. [Epub ahead of print] 106770
      Gestational maternal immune activation (MIA) has been recognized as a risk factor for neurodevelopmental disorders (NDDs) later in life. Furthermore, sex is a significant modifying factor for NDDs. Microglia, the resident immune cells of the brain, appear to be critical mediators of MIA-associated NDD pathology and are known to play a pivotal role in the pathological process of MIA-induced behavioral abnormalities. However, the exact mechanisms linking microglial perturbations to neurodevelopmental abnormalities in adult MIA offspring remain unclear. Here, we demonstrated that MIA induced sex-specific behavioral deficits in male offspring. Bulk RNA sequencing revealed pronounced transcriptional dysregulation related to synaptic transmission and immune responses specifically in males. Single-cell RNA sequencing further indicated that MIA blunted microglial reactivity in the developing prefrontal cortex (PFC) of male offspring. Consistently, further validation confirmed that MIA led to sex-specific synaptic pruning deficits, accompanied by a reduction in the number of proliferating microglia specifically in males during PFC development. As a consequence, male MIA offspring exhibited increased synaptic protein levels in the PFC. Our findings show that impaired microglial activity may contribute to sex-biased neurodevelopmental abnormalities induced by MIA, providing new insights into the neuroimmune mechanisms underlying NDDs.
    Keywords:  Maternal immune activation; Microglia; Neurodevelopmental disorder; Sex differences; Synaptic pruning
    DOI:  https://doi.org/10.1016/j.bbi.2026.106770
  15. Glia. 2026 Jun;74(6): e70163
      Microglial cells are key players in maintaining brain homeostasis and responding to pathological conditions. Their multifaceted roles in health and disease have garnered significant attention in the context of neurodegeneration. In recent years, single-cell transcriptomic techniques have provided unprecedented insights into microglial heterogeneity, revealing distinct subpopulations and gene expression patterns associated with neuroprotection or neurotoxicity. Here, we dissect the transcriptomic landscape of microglia by leveraging human single-nuclei RNA sequencing datasets from multiple neurodegenerative conditions, including Amyotrophic Lateral Sclerosis, frontotemporal dementia, Alzheimer's disease, aging, and Parkinson's disease. This integrative analysis identifies distinct microglial subpopulations, reflecting functional heterogeneity across diseases and reveals a shared cross-disease microglial transcriptional program associated with inflammatory and neurodegenerative processes. Using a machine learning framework, we further demonstrate that this transcriptional program enables robust discrimination between neurodegenerative and control samples. Experimental validation in primary microglia isolated from a mouse model of Niemann-Pick disease type C, also known as juvenile Alzheimer's disease, supports the conservation of key components of this program and highlights Spp1 as a biomarker of disease-associated microglia states. Overall, this study provides an improved portrait of microglia transcriptional remodeling across neurodegenerative disorders and offers a framework for identifying conserved molecular features that may inform therapeutic strategies aimed at modulating microglial activity to mitigate disease progression and foster neuroprotection.
    Keywords:  Niemann‐Pick; SPP1; genomics; macrophages; microglia; neurodegeneration
    DOI:  https://doi.org/10.1002/glia.70163
  16. Acta Neuropathol. 2026 Apr 22. pii: 43. [Epub ahead of print]151(1):
      The aggregation of the microtubule-associated protein tau into oligomeric complexes is strongly correlated with the onset and progression of neurodegeneration in Alzheimer's disease (AD). Increasing evidence implicates nuclear membrane disruption in AD and related tauopathies; however, whether this is a cause or consequence of neurodegeneration remains unresolved. Here, we show that nuclear lamina disruption emerges at the early Braak stages, coinciding with the initial formation of pathological tau aggregates in post-mortem AD brain tissue. Using the tauopathy mouse model (P301S PS19), we demonstrate that oligomeric tau (oTau) directly binds to the Lamin B Receptor (LBR), inducing nuclear envelope invaginations as revealed by electron microscopy. These structural alterations are accompanied by chromatin remodeling and gene expression dysregulation. To dissect the underlying mechanism, we employed a light-inducible OptoTau system (4R1N Tau::mCherry::Cry2Olig) in human iPSC-derived neurons, enabling real-time visualization of tau aggregation dynamics. This system revealed selective recruitment of oTau to the nuclear envelope and direct interactions with LBR and Lamin B2, leading to nuclear deformation and activation of the protein translational stress response. Together, these findings identify nuclear membrane disruption as an early and potentially causative event in tau-mediated neurodegeneration, establishing a mechanistic link between tau oligomerization, nuclear stress, and chromatin remodeling. Targeting nuclear destabilization may offer new therapeutic avenues for mitigating AD pathogenesis.
    Keywords:  Alzheimer’s disease; Nuclear lamina; Nuclear membrane; Oligomerization; Optogenetics; Tauopathy
    DOI:  https://doi.org/10.1007/s00401-026-03018-1
  17. NPJ Parkinsons Dis. 2026 Apr 24.
      RAB12 is a small GTPase and a validated substrate of LRRK2, a kinase genetically linked to Parkinson's disease (PD). While RAB12-LRRK2 signaling has been implicated in ciliogenesis and immune regulation, the neuronal function of RAB12 remains largely unexplored. Here, we investigated the role of RAB12 in synaptic physiology using Rab12 knockout (KO) mice. Rab12 KO mice developed normally but exhibited increased locomotor activity in adulthood. Electrophysiological recordings from striatal slices revealed enhanced presynaptic release probability and increased excitatory drive onto medium spiny neurons. Consistently, live-cell imaging of cultured cortical neurons revealed that Rab12 deletion facilitated, while Rab12 overexpression inhibited, synaptic vesicle exocytosis. Biochemical fractionation showed enrichment of RAB12 in synaptic vesicle-associated fractions containing presynaptic components. Proteomic analysis of Rab12 KO striatal synaptosomes further identified alterations in proteins involved in synaptic membrane trafficking pathways. Together, these findings establish RAB12 as a negative regulator of synaptic vesicle exocytosis and excitatory neurotransmission in vivo. Our study defines a physiological role for RAB12 in synaptic function and provides a basis for future investigation into how LRRK2-dependent RAB12 signaling may contribute to neuronal dysfunction in PD.
    DOI:  https://doi.org/10.1038/s41531-026-01353-4
  18. Neuron. 2026 Apr 23. pii: S0896-6273(26)00270-9. [Epub ahead of print]
      Resident myeloid cells are the main constituents of the healthy central nervous system's (CNS) immune compartment. They usually seed the developing CNS prior to birth, remain there lifelong, and essentially contribute to neuronal network formation and establishment of physiology. While CNS anatomy is optimized for efficient connectivity, function, and maintenance of neuronal cells, distinct structures facilitate selective postnatal immune cell trafficking, including entry of myeloid cells. These myeloid gateways become active upon physiological need, during aging, or in pathologies. As a consequence, individual CNS compartments show variable accessibility to short-living circulating myeloid cells derived from postnatal bone marrow sources. Here, we summarize our current view of myeloid cell trafficking into the healthy CNS, spanning embryogenesis to physiological aging and highlight recent discoveries of novel routes. A precise understanding of the anatomical and molecular properties of myeloid gateways is essential to develop targeted cell therapies to treat myeloid-cell-driven CNS perturbations.
    Keywords:  CAM; blood; brain; interfaces; microglia; monocyte
    DOI:  https://doi.org/10.1016/j.neuron.2026.04.001
  19. Trends Neurosci. 2026 Apr 17. pii: S0166-2236(26)00069-X. [Epub ahead of print]
      In a recent study, Sauvé et al. identified hypothalamic tanycytes as a route for tau transport from cerebrospinal fluid to blood and suggested that disruption of this pathway contributes to Alzheimer's disease pathology. The work broadens current models of tau clearance and raises new questions about how tanycytic dysfunction contributes to neurodegeneration.
    Keywords:  blood–brain barrier; brain clearance; dementia; neurodegeneration; tanycyte; tauopathies
    DOI:  https://doi.org/10.1016/j.tins.2026.03.012
  20. Nature. 2026 Apr 22.
      Focal white matter lesions occur in most neurodegenerative disorders1-3. Despite occurring early in disease, white matter lesions are considered to be independent of, or secondary to, grey matter neuroinflammation, synapse loss and altered neuronal activity4-7. Notably, their functional effect on neuronal circuits remains understudied. To address this, we generated a focal white matter lesion in the rat brain within a clinically relevant, anatomically well-defined circuit, in which these lesions occur in many neurodegenerative disorders8-10. Here we show that focal white matter lesions evoke transient neuronal activity changes and microgliosis, with subsequent synapse loss and increased microglial engulfment in the grey matter, which is reversed if myelin regeneration completes. Grey matter microgliosis is often considered to be detrimental; however, we show that it is an integral part of regeneration and is conserved across three distinct mouse circuits and lesioning methods. Preventing these transient changes in the grey matter blocks myelin regeneration in the white matter. Conversely, inducing myelin regeneration failure leads to chronic grey matter neuroinflammation. This recapitulates the low-grade inflammation considered to be a dominant mechanism underlying neurodegeneration7,11,12. Our findings reveal a form of regenerative plasticity coupling white matter integrity to grey matter function, which may underlie multiple neurodegenerative conditions, and highlight the potential of targeting myelin regeneration to prevent chronic neuroinflammation.
    DOI:  https://doi.org/10.1038/s41586-026-10414-w
  21. Sci Transl Med. 2026 Apr 22. 18(846): eadu3761
      Diabetes mellitus (DM) accelerates vascular diseases including peripheral arterial disease (PAD). Endothelial cells (ECs) and macrophages (MΦs) are important contributors to DM-associated vascular dysfunction, both individually and through reciprocal cross-talk. Although single-cell profiling has revealed the heterogeneity of ECs and MΦs, how this diversity translates into cell-cell interactions, and consequentially vascular function, remains unclear. We leveraged single-cell RNA sequencing and spatial transcriptomics to profile human mesenteric arteries from non-diabetic donors and from donors with type 2 diabetes (T2D), generating a transcriptome and interactome atlas of diabetic vasculature. This analysis identified triggering receptor expressed on myeloid cells 2 (TREM2) as one of the top T2D-induced genes in mononuclear phagocytes (MPs), with concomitant increases in TREM2 ligands in ECs. TREM2+ MPs exhibited foam cell-like features but acquired a proinflammatory gene profile in DM. Functionally, TREM2 inhibition in vitro attenuated proinflammatory responses in MPs and ECs and enhanced EC migration. In streptozotocin- and high-fat high-sucrose diet-induced mouse models of diabetes with hindlimb ischemia (a model of PAD), TREM2 blockade using a neutralizing antibody improved perfusion recovery, whereas TREM2 activation with an agonist exacerbated ischemic injury. Analysis of clinical samples confirmed elevated EC-TREM2 signaling in human PAD, particularly in the setting of DM, highlighting its translational relevance. Collectively, our study presents an atlas of human diabetic vessels with single-cell and spatial resolution, identifying TREM2-EC interaction as a driver of diabetic vasculopathy and a potential therapeutic target in DM-associated PAD.
    DOI:  https://doi.org/10.1126/scitranslmed.adu3761
  22. PLoS Pathog. 2026 Apr;22(4): e1014056
      Heterogeneous Nuclear Ribonucleoprotein K (hnRNP K) is a limiting factor for prion propagation. However, little is known about the function of hnRNP K except that it is essential to cell survival. Here, we performed a synthetic-viability CRISPR ablation screen to identify epistatic interactors of HNRNPK. We found that deletion of Transcription Factor AP-2γ (TFAP2C) suppressed the death of hnRNP K-depleted LN-229 and U-251 MG cells, whereas its overexpression hypersensitized cells to hnRNP K loss. HNRNPK ablation decreased cellular ATP, downregulated genes related to lipid and glucose metabolism, and enhanced autophagy. Co-occurrent deletion of TFAP2C reversed these effects, restoring transcriptional balance and alleviating energy deficiency. We linked HNRNPK and TFAP2C functional and genetic interaction to mTOR signaling, observing that hnRNP K depletion inhibited mTORC1 activity through downregulation of mTOR and Rptor, while TFAP2C overexpression enhanced mTORC1 downstream functions. In prion-infected cells, TFAP2C activation reduced prion levels and countered the increased prion propagation caused by HNRNPK suppression. Short-term inhibition of mTORC1 also elevated prion levels and partially mimicked the effects of HNRNPK silencing. Our study identifies TFAP2C as a genetic interactor of HNRNPK, implicates their roles in mTOR metabolic regulation, and establishes a causative link between these activities and prion propagation.
    DOI:  https://doi.org/10.1371/journal.ppat.1014056
  23. Sci Adv. 2026 Apr 24. 12(17): eadw4136
      Directional cues are essential for orienting cells during tissue morphogenesis and repair. In peripheral nerve regeneration, Schwann cells (SCs) align longitudinally in the nerve bridge to guide axonal pathfinding, but the mechanisms are not fully understood. We show here that after nerve injury, activated SCs up-regulate the guidance receptor Plexin-B1, enabling membrane plasticity required for SC polarization and longitudinal alignment along the axons. Aligned axon-SC provides positional cues to orient macrophages and extracellular matrix. Loss of Plexin-B1 disrupts SC morphological transformation, contact inhibition of locomotion between SCs, and axon-SC alignment, leading to SC misorientation, excessive inflammation, and delayed axon regeneration and functional recovery. These findings identify Plexin-B1 as a key orchestrator to orient SCs by regulating both SC-SC and axon-SC interactions during nerve repair. Elucidating the mechanisms of spatial guidance in nerve repair after injury has potential implications for therapeutic strategies to enhance neural regeneration.
    DOI:  https://doi.org/10.1126/sciadv.adw4136
  24. Nature. 2026 Apr 22.
      Neuronal axons have traditionally been considered to be the primary mediators of functional connectivity among brain regions. However, the role of astrocyte-mediated communication has been largely underappreciated. Astrocytes communicate with one another through gap junctions, but the extent and specificity of this communication remain poorly understood. Astrocyte gap junctions are necessary for memory formation1,2, synaptic plasticity3-5, coordination of neuronal signalling6, and closing the visual and motor critical periods7,8. These findings indicate that this form of communication is essential for proper central nervous system development and function. Despite the importance of astrocyte gap junctional networks, studying them has been challenging. Current methods such as slice electrophysiology disrupt network connectivity and introduce artefacts due to tissue damage. Here, we developed a vector-based approach that labels molecules as they are fluxed by astrocyte gap junctions in awake, behaving animals to overcome these limitations. We then used whole-brain tissue clearing9,10 to image these intact, three-dimensional astrocyte networks. We show that multiple astrocyte networks traverse the mouse brain. These networks selectively connect specific regions, rather than diffusing indiscriminately, and vary in size and organization. We observe local networks that are confined to single brain regions and long-range networks that robustly interconnect multiple regions across hemispheres, often exhibiting patterns distinct from known neuronal networks. We also demonstrate that astrocyte networks undergo structural reorganization in the adult brain after sensory deprivation. These findings reveal a mode of communication between distant brain regions that is mediated by plastic networks of gap junction-coupled astrocytes.
    DOI:  https://doi.org/10.1038/s41586-026-10426-6
  25. Proc Natl Acad Sci U S A. 2026 Apr 28. 123(17): e2531597123
      The presence of neuromelanin is a characteristic feature of the human substantia nigra (SN); however, the mechanism of its synthesis and its role in the development of Parkinson's disease remain unclear. Here, we report that the host defense enzyme lactoperoxidase (LPO), which possesses broad antimicrobial activity on mucosal surfaces, is selectively expressed in human dopaminergic neurons, a feature not shared by the rodent SN. We also demonstrate that LPO can catalyze multiple steps of melanin formation in vitro, and transgenic expression of human LPO in the rat SN induces the appearance of neuromelanin. Based on our results, LPO likely contributes to neuromelanin formation in the SN. Since LPO degrades H2O2 during neuromelanin synthesis, the enzyme's activity represents a previously unrecognized link between neuromelanin formation and antioxidant defense mechanisms.
    Keywords:  Parkinson’s disease; hydrogen peroxide; lactoperoxidase; neuromelanin
    DOI:  https://doi.org/10.1073/pnas.2531597123
  26. Biochem Pharmacol. 2026 Apr 19. pii: S0006-2952(26)00327-8. [Epub ahead of print]250(Pt 1): 117994
      Once viewed as a homogenous population, microglia are now understood to exist as a dynamic continuum of functionally distinct states whose existence is supported by accumulating evidence from multiple experimental approaches. This heterogeneity, spanning molecular, morphological, and metabolic dimensions, is actively sculpted by brain region, life stage, and a complex microenvironment of neuronal, astrocytic, and systemic signals. In neurological disorders such as Alzheimer's disease, this plasticity leads to context-dependent diversification into discrete subsets-ranging from protective, phagocytic phenotypes to detrimental, inflammatory ones-that critically influence disease progression. Decoding this heterogeneity through single-cell and spatial omics provides a new pharmacological blueprint: it reveals key druggable nodes (e.g., TREM2, CD14) that govern pathogenic state transitions and informs the rational design of subset-selective delivery systems (e.g., ligand-directed nanocarriers). However, translating these insights requires overcoming persistent challenges, including species differences between mouse and human microglia, a lack of tools for causal subset manipulation, and the integration of spatial with temporal dynamics. By framing microglial heterogeneity as a central targetable axis, this review outlines a pathway for developing precise, state-modulating therapeutics to intervene in neurodegeneration and neuroinflammation.
    Keywords:  Functional states; Microglial heterogeneity; Neurodegeneration; Neuroinflammation; Spatiotemporal dynamics
    DOI:  https://doi.org/10.1016/j.bcp.2026.117994
  27. Free Radic Biol Med. 2026 Apr 16. pii: S0891-5849(26)00313-8. [Epub ahead of print]251 212-228
      Tauopathies encompass a diverse group of neurodegenerative disorders characterized by abnormal TAU accumulation, synaptic dysfunction, neuroinflammation, and progressive neuronal loss. Beyond its role as a pathological hallmark, increasing evidence indicates that TAU actively drives neurodegeneration by disrupting mitochondrial function, promoting oxidative stress, and triggering maladaptive innate immune responses. In this context, pyroptosis, a highly inflammatory form of programmed cell death mediated by inflammasome activation and GASDERMIN pore formation, has emerged as a critical mechanism linking TAU pathology to chronic neuroinflammation and neuronal damage. This review summarizes current advances on the molecular crosstalk between TAU pathology, redox imbalance, inflammasome signaling, and pyroptotic cell death across primary and secondary tauopathies, including Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD). We discuss how pathological TAU induces mitochondrial dysfunction and reactive oxygen species generation, providing key priming and activation signals for inflammasomes, particularly NLRP3, in microglia and other brain cells. Pyroptosis is highlighted as a downstream effector that amplifies neuroinflammation through the release of pro-inflammatory cytokines and danger-associated molecular patterns, thereby sustaining TAU propagation and neurodegeneration. Special attention is paid to the redox-sensitive transcription factor NRF2 as a central regulatory node capable of counteracting oxidative stress, inflammasome activation, and pyroptosis. Finally, we examine emerging therapeutic strategies targeting pyroptotic and redox pathways, discussing their translational potential and current limitations. Overall, this review positions pyroptosis-driven redox-immune dysregulation as a promising yet underexplored therapeutic target in TAU-driven neurodegenerative diseases.
    Keywords:  Inflammasome; NRF2; Neurodegeneration; Neuroinflammation; Oxidative stress; Pyroptosis; Redox signaling; TAU
    DOI:  https://doi.org/10.1016/j.freeradbiomed.2026.04.029
  28. Lancet Neurol. 2026 May;pii: S1474-4422(26)00127-4. [Epub ahead of print]25(5): 437-438
      
    DOI:  https://doi.org/10.1016/S1474-4422(26)00127-4
  29. Neuron. 2026 Apr 22. pii: S0896-6273(26)00265-5. [Epub ahead of print]
      The combination of brain glucose hypometabolism and hyperphosphorylated Tau (p-Tau) pathology is the strongest known clinical predictor of imminent cognitive decline, yet how these factors cooperate to drive dementia remains unknown. Here, we show that glucose hypometabolism synergizes with p-Tau to trigger neuronal loss through necroptosis. Under low-glucose conditions, accumulated p-Tau forms a molecular scaffold that directly recruits RIPK1, while concomitant loss of the necroptosis checkpoint A20 removes a critical brake on this death pathway. This dual mechanism thereby precipitates neuronal necroptosis. Restoring A20 expression with acetyl-L-carnitine or preventing the p-Tau-RIPK1 interaction using a RIPK1-derived competitive peptide alleviates neuronal necroptosis and brain atrophy in a Tau transgenic mouse model. Collectively, our findings uncover a previously unrecognized metabolism-driven necroptotic signaling cascade initiated by a p-Tau-RIPK1 hub, providing mechanistic insight into how glucose hypometabolism synergizes with p-Tau to drive neurodegeneration.
    Keywords:  glucose hypometabolism; necroptosis; neurodegeneration; p-Tau
    DOI:  https://doi.org/10.1016/j.neuron.2026.03.035
  30. Sci China Life Sci. 2026 Apr 17.
      TGF-β-activated kinase 1 (TAK1) is a key signaling hub and drug target in inflammatory responses. Although metabolism has been critically linked to immune cell function and inflammation, the metabolic control of TAK1 activation and intervention strategy remains to be explored. Here, we show that SM934, a derivative of the traditional Chinese medicine artemisinin, inhibits inflammatory responses via targeting α-enolase and inhibiting metabolite phosphoenolpyruvate (PEP) production. PEP directly binds TAK1 and inhibits its ubiquitination at the lysine-72 site, which promotes NF-κB activation and inflammatory responses. Overall, our study demonstrates a metabolic control of TAK1 stabilization and proposes that it could be disrupted by the derivative of the natural product artemisinin.
    Keywords:  PEP; SM934; TAK1; artemisinin derivative; inflammation; α-enolase
    DOI:  https://doi.org/10.1007/s11427-025-3167-7