bims-cediti Biomed News
on Cell death in innate immunity, inflammation, and tissue repair
Issue of 2026–06–21
eighteen papers selected by
Kateryna Shkarina, Universität Bonn



  1. Nat Commun. 2026 Jun 15.
      SARS-CoV-2 typically utilises host receptor angiotensin-converting enzyme 2 (ACE2) for viral entry. Despite low ACE2 expression, monocyte-derived macrophages, the predominant lung macrophage during severe COVID-19, are often found with SARS-CoV-2 in infected lungs. As macrophage inflammation and cytokine storm are key immunopathological events that drive severe COVID-19, insights into mechanisms underlying viral entry into macrophages are critical to devise novel COVID-19 therapies. Mounting evidence supports that COVID-19 pathogenesis is associated with apoptosis, a type of programmed cell death which releases large extracellular vesicles called apoptotic bodies (ApoBDs). Here, we show that ApoBDs from SARS-CoV-2-infected cells carried infectious virions. Macrophages efferocytose these ApoBDs, enabling SARS-CoV-2 entry and pro-inflammatory responses including inflammasome and NF-κB signalling. To demonstrate targetability of this ApoBD efferocytosis-mediated viral entry, we screen for inhibitors of SARS-CoV-2-induced ApoBD formation and identified T-type voltage-gated calcium channel (T-channel) blockers. Mechanistically, T-channel blockers impair the extracellular calcium influxes required for ApoBD biogenesis. Importantly, blockade of ApoBD formation by T-channel blockers is able to limit cell-to-cell viral transmission, macrophage inflammation and lung immunopathology. Our discovery reveals a novel route for SARS-CoV-2 infection and cytokine storm induction, expanding our understanding of COVID-19 pathogenesis and demonstrating a therapeutic target for infectious diseases.
    DOI:  https://doi.org/10.1038/s41467-026-74363-8
  2. Front Cell Dev Biol. 2026 ;14 1814812
      Pyroptosis is a lytic form of regulated cell death driven by inflammasome activation and gasdermin-mediated membrane rupture, characterized by robust inflammatory amplification. High-mobility group box 1 (HMGB1), a multifunctional nuclear protein and damage-associated molecular pattern, has emerged as a central regulator within pyroptosis-associated pathologies. Acting both as a downstream alarmin released during pyroptotic cell death and as an upstream licensing factor for inflammasome activation and innate immune signaling, HMGB1 establishes a context-dependent feedforward loop that shapes tissue injury and immune responses. In infectious and inflammatory disorders, excessive HMGB1 release exacerbates immune dysregulation and organ damage, whereas in selected tumor settings, pyroptosis-associated HMGB1 contributes to immunogenic cell death and antitumor immunity. This review systematically summarizes the molecular mechanisms underlying HMGB1-regulated pyroptosis, including canonical and noncanonical inflammasome pathways, gasdermin execution, and crosstalk with other regulated cell death programs. We further integrate evidence implicating the pyroptosis-HMGB1 axis across systemic diseases involving the nervous, respiratory, digestive, circulatory, urinary, locomotor, endocrine, reproductive, and immune systems. Finally, we discuss emerging therapeutic strategies targeting this axis, highlighting opportunities and challenges for disease-specific and precision interventions.
    Keywords:  HMGB1; gasdermins; inflammasomes; pyroptosis; regulated cell death; systemic diseases
    DOI:  https://doi.org/10.3389/fcell.2026.1814812
  3. Infect Immun. 2026 Jun 15. e0017826
      Many intracellular pathogens stimulate host cell stress by directly or indirectly causing an imbalance in host nutrients. Depletion of amino acid pools, in particular, can act as a danger signal to infected cells. Using a restrictive host model of Salmonella enterica serovar Typhi (S. Typhi) infection, we identify early induction of the integrated stress response (ISR) by viable bacteria, but not by heat-killed bacteria. Genetic deletion of the amino acid-sensing ISR kinase GCN2 (also known as EIF2AK4) prevented early ISR activation during S. Typhi infection and murine macrophages lacking GCN2 show impaired bacterial clearance and decreased cytokine output. Supplementation of wild-type C57BL/6 murine macrophages with only the non-essential amino acid asparagine was sufficient to suppress S. Typhi-induced ISR activation, and deletion of S. Typhi ansB, encoding an asparaginase, prevented ISR activation during infection. Pharmacological inhibition of mammalian target of rapamycin (mTOR), the other major amino acid-sensing pathway in eukaryotic cells, prevented GCN2 activation and ISR induction in murine macrophages, indicating an upstream role for mTOR in signaling to GCN2. These findings suggest a role for the ISR in macrophage innate immune responses to S. Typhi infection and highlight a potential difference in nutrient-dependent signaling between the S. Typhi-susceptible human host and the restrictive murine host centered around asparagine, mTOR, and GCN2.
    Keywords:  gram-negative bacteria; innate immunity; nutritional immunity
    DOI:  https://doi.org/10.1128/iai.00178-26
  4. Microbiol Spectr. 2026 Jun 18. e0412125
      Mycobacterium tuberculosis (Mtb) has been known to evade host innate immunity by manipulating macrophage function. Interleukin-1β (IL-1β) is a cytokine secreted by macrophages as a consequence of inflammasome activation. Mtb can inhibit activation of the NLRP3 and AIM2 inflammasomes and subsequent pyroptosis. The capacity of Mtb to manipulate other types of inflammasomes is unknown. In this study, we investigated whether Mtb or the nontuberculous mycobacteria Mycobacterium kansasii (Mkan) and Mycobacterium smegmatis (Msmeg) can inhibit the NLRP1 or pyrin inflammasomes. We show that none of the mycobacteria consistently inhibit the NLRP1 inflammasome after it is activated by priming with lipopolysaccharide (LPS) and treatment with 1G244 in human macrophages. Similarly, neither Mtb nor the NTMs inhibit the pyrin inflammasome after it is activated by priming with LPS and treating with TcdB toxin from Clostridium difficile in human macrophages. In murine macrophages, Mkan shows inhibition only at 3 h post-infection, and Msmeg, only at 24 h post-infection, whereas no inhibition was observed at any time point for Mtb. In conclusion, our main findings are that Mtb is unable to inhibit the NLRP1 and the pyrin inflammasomes in human macrophages.IMPORTANCEThe research focuses on the interaction of mycobacteria with BMDMs and hMDMs regarding NLRP1 and pyrin inflammasome inhibition. We think that these results point to insights into the pathways of pathogen recognition in macrophages, which may have broader implications for host defense. These results are technically sound and provide new information to the field by showing that various mycobacteria do not inhibit the NLRP1 and Pyrin inflammasomes, at least under our specific experimental settings. Important limitations to the study are its narrow scope and limited mechanistic depth.
    Keywords:  host-pathogen interactions; immunology; inflammasome; innate immunity; macrophages; microbiology; mycobacteria
    DOI:  https://doi.org/10.1128/spectrum.04121-25
  5. Nat Commun. 2026 06 15. pii: 5288. [Epub ahead of print]17(1):
      Pancreatic ductal adenocarcinoma (PDAC) is projected to become the second leading cause of cancer-related death within this decade. Here, we show that its major driver oncogene KRAS activates the cGAS-STING-TBK1 axis, inducing a type I interferon (IFN) response that primes PDAC cells for necroptosis. Using genetically engineered mouse models, we find that cancer cell-specific deletion of caspase-8 is sufficient to trigger necroptotic cell death, eliminating most pancreatic precursor lesions. Mechanistically, KRAS-driven IFN signalling induces ISGF3-dependent expression of necroptosis-related interferon-stimulated genes, including MLKL. This renders PDAC cells selectively vulnerable to necroptosis upon caspase-8 inhibition. Therapeutically, pharmacologic caspase inhibition reduces tumour burden in aggressive PDAC models and human patient-derived organoids. A pan-cancer transcriptomic analysis links necroptosis gene expression with Ras pathway activity and IFN signatures across multiple tumour types. These findings reveal a KRAS-induced IFN program that sensitises tumour cells to necroptosis, highlighting a therapeutic vulnerability in PDAC with broader relevance across IFN-activated cancers.
    DOI:  https://doi.org/10.1038/s41467-026-73189-8
  6. mBio. 2026 Jun 15. e0101326
      Viruses transit from a low to high multiplicity of infection (MOI) regime in infected tissues. Type-1 interferons (IFNs) enforce a cellular state refractory to virus multiplication, while the death of infected cells eliminates viral replicative niche. Here, we investigated how these two innate antiviral mechanisms cooperate at various MOIs upon cell infection by Chandipura virus (CHPV), a cytopathic RNA virus implicated in several outbreaks of acute encephalitis in India. We found that as expected, a gradual increase in the input MOI from 0.02 to 2 led to a proportionate surge in the viral yield. Surprisingly, a further rise to MOI 20 caused a reduction in the progeny titer. Our mathematical modeling together with ex vivo infection studies involving knockout cells suggested that cell death-more so than virus-induced type-1 IFNs-restricted CHPV propagation at cell-saturating high MOIs, leading to a net fall in the yield at MOI 20. We argue that the distinct involvement of innate immune pathways at varied MOIs imparts robust cellular defense against cytopathic viruses.
    IMPORTANCE: After host invasion, a limited number of viruses initially provide for a low multiplicity of infection (MOI) of tissue cells. Ongoing viral multiplication allows for high multiplicity infection of host cells at a later stage. Type-1 IFNs and cell death constitute two principal arms of the antiviral cellular defense. We probed infection of cultured cells by Chandipura virus (CHPV), a virus implicated in encephalitis outbreaks, at various MOI. We find that CHPV propagation is restricted mainly through type-1 IFNs at low MOI and cell death at high MOI. Cell death not only destroys the viral replicative niche but also orchestrates pathological inflammation. In fact, moderating inflammation represents an important objective in the symptomatic management of viral diseases. While the proposed model needs to be tested for other viruses, our findings may bear significance for therapeutic intervention strategies and timing in viral diseases.
    Keywords:  Chandipura virus; antiviral defense; burst size; cell death; interferon-β; multiplicity of infection; type-1 interferons; virus propagation
    DOI:  https://doi.org/10.1128/mbio.01013-26
  7. J Virol. 2026 Jun 17. e0011426
      Poxviruses encode a plethora of proteins adapted to diverse cellular responses against viruses. The poxvirus-encoded E3-like proteins are multifunctional, regulating diverse cellular antiviral responses. The canonical Vaccinia E3-like proteins have two domains: an N-terminal Z-form nucleic acid-binding domain (Zα-BD) and a C-terminal double-stranded RNA-binding domain (dsRNA-BD). Using protein sequence and structural homology modeling, we identified dsRNA-BD-fold-containing proteins in all the poxviruses except avipoxviruses, salmon poxvirus, and entomopoxviruses. Furthermore, we show that the acquisition of these proteins likely happened under three distinct events and can be classified into three categories: (i) the E3-like proteins with dsRNA-BD with the presence or absence of the N-terminal domain; (ii) unconventional/putative dsRNA-BD-fold-like proteins, present in macropoxvirus and molluscipoxvirus, and (iii) the dsRNA-BD-containing protein present in crocodile poxvirus. Members of leporipoxvirus, waddenpoxvirus, cetaceanpoxvirus, and selected members of orthopoxvirus contain E3-like proteins missing the N-terminal Zα-BD required for necroptosis inhibition. Using AlphaFold, we also show that the Zα-BD of chordopoxviruses, E3-like proteins, is structurally more variable than the dsRNA-binding domain. Compared to orthopoxviruses that inhibit necroptosis and contain an N-terminus Zα-BD, our results show that leporipoxviruses induce receptor-interacting protein kinase (RIPK) RIPK1- and RIPK3-mediated necroptosis in human and mouse necroptosis-competent cell lines. These data suggest that leporipoxviruses lack countermeasures against necroptosis, unlike orthopoxviruses, which encode multiple key regulators of necroptosis, possibly due to a lack of selective pressure in their lagomorph host species.IMPORTANCEThe evolutionary arms race between viruses and their hosts has led to the viral acquisition of genes that antagonize the host's antiviral defenses. However, related viral and host proteins have evolved under positive, purifying, and neutral selection. Poxvirus-encoded E3-like proteins play a pivotal role in regulating the host's cellular antiviral and apoptotic responses. The two domains of canonical E3-like proteins, an N-terminal Z-form nucleic acid-binding domain (Zα-BD) and a C-terminal double-stranded RNA-binding domain (dsRNA-BD), have evolved under varying host immune selection pressures. Here, we demonstrate that the dsRNA-BD is structurally conserved among E3 orthologs, whereas the Zα-BD, involved in regulating necroptosis, exhibits structural diversity and is absent in some poxviruses. Leporipoxviruses, which lack Zα-BD-containing proteins and evolved in species without functional necroptosis, do activate necroptosis in necroptotic-competent cells. Our study thus highlights that a lack of selective pressure from the host can shape viral countermeasures and viral divergence.
    Keywords:  MYXV; cell death; dsRNA-binding proteins; myxoma virus; necroptosis; poxvirus
    DOI:  https://doi.org/10.1128/jvi.00114-26
  8. Trends Immunol. 2026 Jun 19. pii: S1471-4906(26)00139-0. [Epub ahead of print]
      Inflammation is a metabolically intensive and tightly regulated process, driven primarily by innate immune cells. Cellular metabolism actively instructs immune signaling and cell fate decisions. Bioenergetic pathways, including glycolysis, mitochondrial respiration, and the tricarboxylic acid cycle, reshape cytokine production and regulate inflammatory cell death pathways. In this review, we synthesize emerging evidence on how metabolic intermediates and pathways regulate inflammasome signaling and the execution of diverse inflammatory cell death modalities, including pyroptosis, necroptosis, PANoptosis, and ferroptosis. We propose that metabolic inputs-including redox balance, mitochondrial dynamics, and lipid modifications-constitute an interconnected metabolic regulatory network that determines the threshold and outcome of inflammatory signaling. This framework offers new insights into immunometabolic dysregulation and therapeutic strategies in inflammatory, infectious, and neoplastic diseases.
    Keywords:  PANoptosis; ferroptosis; inflammation; metabolic nodes; necroptosis; pyroptosis
    DOI:  https://doi.org/10.1016/j.it.2026.06.002
  9. Nat Immunol. 2026 Jun 15.
      The pathogenic mechanisms underlying pyoderma gangrenosum (PG) remain unclear. Here we report three patients with PG from two unrelated kindreds with homozygous R57C mutation of the linear deubiquitinase OTULIN. The patients have isolated, pediatric-onset, OTULIN-related PG (ORP). In contrast to OTULIN-related autoinflammatory syndrome (ORAS), caused by mutations affecting the catalytic domain, R57C affects the PUB-interacting motif with distinct biochemical, immunological and clinical consequences. OTULIN-R57C is catalytically active but is unable to bind the linear ubiquitin assembly complex (LUBAC). Patient monocytes show heightened expression of IL1B, and OTULIN-R57C fails to suppress inflammasome activity. Patients have elevated levels of TNF, and their dermal fibroblasts show heightened susceptibility to TNF-dependent cell death. Homozygosity for OTULIN-R57C leads to accumulation of linear ubiquitin and LUBAC autoubiquitination in patients' dermal fibroblasts, consistent with pathogenic LUBAC activity. These findings identify a genetic etiology of isolated PG of childhood. We propose a multifactorial mechanism of ORP, including myeloid IL-1β production and TNF-driven death of skin-resident cells, suggesting that blockade of IL-1β or TNF are therapeutic options in PG.
    DOI:  https://doi.org/10.1038/s41590-026-02568-6
  10. Cell Syst. 2026 Jun 19. pii: S2405-4712(26)00129-8. [Epub ahead of print] 101647
      Trained immunity (a form of innate immune memory) is defined in part by heightened responses to pathogen restimulation and can be generated by many different stimuli. However, both the quantitative differences in trained states generated by different stimuli and the downstream consequences of those differences remain unclear. Here, we used primary human monocyte-derived macrophages to demonstrate phenotypic and molecular stimulus specificity of trained immunity 6 days after initial exposure. Quantification of cytokine production with single-molecule RNA imaging revealed stimulus-specific patterns of response to restimulation, with trained cells showing stronger responses to secondary stimuli more similar to their initial stimulation. Differential licensing of inflammatory transcription factors was associated with encoding of specificities in chromatin 6 days after training, while memory of some, but not all, training stimuli was lost by 11 days post-training in vitro. Overall, our findings demonstrate that different training stimuli can impart specific memories that generate distinct training phenotypes.
    Keywords:  cellular learning; cellular memory; epigenetics; innate immune memory; innate immunity; macrophages; single-cell analysis; systems biology; trained immunity
    DOI:  https://doi.org/10.1016/j.cels.2026.101647
  11. RNA Biol. 2026 Jun 18.
      Since their discovery, Z-nucleic acids (Z-NAs), which adopt a left-handed double helical conformation, have puzzled researchers regarding their physiological functions. These unusual nucleic acids are recognized by proteins containing Zα domains, particularly Z-DNA binding protein 1 (ZBP1) and adenosine deaminase acting on RNA 1 (ADAR1). Utilizing mouse genetics with knockout models and site-specific Zα domain mutations, scientists have revealed that Z-NAs serve as critical regulators of programmed cell death, inflammation, antiviral immunity, and anti-tumour responses. This review systematically examines mechanistic insights from Zbp1- and Adar1-mutant models, illuminating how Z-NAs play a dual role as essential triggers of host defence and as potential drivers of autoinflammatory diseases.
    Keywords:  Z-nucleic acid; Zα domain; cell death; inflammation
    DOI:  https://doi.org/10.1080/15476286.2026.2691476
  12. Nat Struct Mol Biol. 2026 Jun;33(6): 1011-1019
      Scramblases are physiologically important proteins that translocate phospholipids bidirectionally across cell membranes. For example, scrambling facilitated by dimers of the voltage-dependent anion channel 1 (VDAC1) enables endoplasmic reticulum-derived phospholipids to cross the outer membrane to enter mitochondria. Here we describe a protocol to obtain lipid translocation rates at a single-protein level, allowing for mechanistic understanding of scramblases. We reconstituted vesicles with fluorescent phospholipids and VDAC1 dimers and use high-throughput imaging to quantify their size and dimer content. We measure scrambling in each vesicle using a new assay and find that individual human VDAC1 dimers scramble lipids at rates ranging from under 100 to over 10,000 per second. This kinetic heterogeneity, masked in ensemble measurements, revealed that rapid scrambling is facilitated by specific VDAC1 dimers. Extending our analyses to bovine opsin, a monomeric G-protein-coupled receptor scramblase, we demonstrate the versatility of our platform for quantifying lipid scrambling and exploring its regulation.
    DOI:  https://doi.org/10.1038/s41594-026-01821-8
  13. J Immunol. 2026 Jun 07. pii: vkag116. [Epub ahead of print]215(6):
      Interferon-gamma (IFN-γ) is a powerful transactivating signal eliciting hundreds of IFN-stimulated genes (ISGs) in humans to help combat infection. Most ISGs remain uncharacterized, and here we searched for actin-binding candidates that could potentially target intracellular pathogens to block their spread or promote immune cell migration into infected tissues. Dual RNA-Seq and in silico mining across 1,933 data sets discovered >225 actin-related genes; the most highly expressed was XIRP1 (xin actin binding repeat containing 1 protein), a new ISG with no reported immune function. We found XIRP1 induction required IFN-γ plus IL-1β or exposure to pathogenic Listeria, Shigella, or Salmonella in immune and non-immune cells. Within IFN-γ-activated human macrophages, the XIRP1 protein localized to actin-rich podosomes where it formed a dome-shaped cap facing the cytosol; genetic XIRP1 ablation led to significant actin loss from these structures. Within infected cells, XIRP1 was recruited onto cytosolic Listeria monocytogenes in an ActA-dependent manner. Live imaging found many listeriae were fully encapsulated by XIRP1 whereas incomplete XIRP1 coating allowed pathogen escape from the initial coat structure. Together, our results identify XIRP1 as a new podosome-associated ISG that targets cytosolic bacteria as part of the IFN-γ-induced defense program in humans.
    Keywords:  actin; cell-autonomous immunity; interferon; podosomes
    DOI:  https://doi.org/10.1093/jimmun/vkag116
  14. J Immunol. 2026 Jun 07. pii: vkag146. [Epub ahead of print]215(6):
      In inflammatory tissue niches, macrophages encounter intense oxidative stress due to their own production of reactive oxygen and nitrogen species as part of antimicrobial defense. Our findings reveal that inflammatory macrophages deploy distinct, context-dependent redox-protective mechanisms to survive this self-inflicted stress, thereby avoiding ferroptotic cell death. Specifically, LPS-activated macrophages, M(LPS), rely on the GTP cyclohydrolase 1 (GCH1)-tetrahydrobiopterin (BH4) pathway for ferroptosis resistance, whereas LPS + IFN-γ-activated macrophages, M(LPS-IFN-γ), depend primarily on nitric oxide produced by inducible nitric oxide synthase (iNOS)-with the BH4 pathway suppressing cell death in the absence of nitric oxide. These distinct adaptations highlight a novel GCH1-BH4-iNOS axis that governs macrophage ferroptosis susceptibility. In both the LPS or the LPS + IFN-γ-activated settings, the redox-protective phenotype is reversible: Removal of inflammatory stimuli abolishes the protection, indicating that this metabolic programming requires continuous stimulation and is not a permanently fixed state. These findings uncover redox metabolism-guided metabolic distinctions between inflammatory macrophages and reveal how they preserve viability over prolonged inflammatory activation. Ultimately, our findings establish the GCH1-BH4-iNOS axis as a central, targetable mechanism to manipulate macrophage ferroptosis resistance for therapeutic purposes.
    Keywords:  lipopolysaccharide; monocytes/macrophages; nitric oxide
    DOI:  https://doi.org/10.1093/jimmun/vkag146
  15. EMBO Rep. 2026 Jun 15.
      HIV infection is accompanied by chronic inflammation-related co-morbidities, even when viral replication is suppressed by therapy. This persistent inflammatory state suggests that long-lived immune cell lineages may acquire stable pro-inflammatory programming. Here, we investigate whether inflammatory programming can be imprinted within hematopoietic lineages, following the exposure of mice and bone marrow-derived macrophages (BMDMs) to extracellular vesicles (EVs) carrying Nef, a key inflammatory factor of HIV. Multi-omics profiling shows that hematopoietic cells exposed to Nef-EVs undergo epigenetic remodeling and reprogramming of energy and lipid metabolism characteristic of trained innate immunity. The inflammatory phenotype in BMDMs is partially reversed by inhibition of glycolysis, a key metabolic driver of trained immunity. We demonstrate that following competitive bone marrow transplantation, hematopoiesis in mice receiving bone marrow from Nef-EV-treated donors displays a sustained bias toward myelopoiesis, and BMDMs retain enhanced inflammatory potential. These findings demonstrate that Nef-EVs can imprint a lasting inflammatory memory, mechanistically similar to trained immunity, in hematopoietic cells. This memory persists beyond the initial exposure and may contribute to chronic inflammation in people with HIV.
    DOI:  https://doi.org/10.1038/s44319-026-00838-w
  16. J Clin Invest. 2026 06 15. pii: e207022. [Epub ahead of print]136(12):
      Traumatic brain injury (TBI) disproportionately kills and disables older adults, yet the biology driving this vulnerability remains unresolved. In this issue of the JCI, Lu et al. combined single-cell transcriptomics, metabolomics, and chromatin profiling in mice, validated in human TBI tissue, to define an age-dependent microglial dichotomy. They report that an NLRP3+/IL-1β-linked state dominates the aged brain, while a Lysozyme+/Lyz2+ state predominates in the young. Microglia-targeted perturbation of NLRP3 and ELF1 each shifted the balance and improved survival in mouse models of TBI, and the repurposed drug Imeglimin improved outcomes in these models, confirming that this pathway is druggable. By connecting NLRP3 inflammasome dominance, ELF1-driven transcription, and glycolytic reprogramming to the loss of a protective Lyz2+ response, this work converts age from a clinical risk factor to a set of druggable microglial targets.
    DOI:  https://doi.org/10.1172/JCI207022
  17. Nat Commun. 2026 Jun 17.
      Epithelia likely predate the last common animal ancestor, yet the evolutionary origin and nutritional regulation of epithelial remodelling remain poorly understood. Here, we show that extensive, starvation-induced cell loss in the sea anemone Nematostella vectensis is associated with epidermal cell extrusion. This process involves formation of a rosette-like arrangement in which an apoptotic, extruding cell is surrounded by a phospho-ERK1/2-positive ring of cells, accompanied by basal translocation of adherens junction components. Combining chemical perturbations with computational quantification of extrusion and cell density, we show that apoptosis is necessary but not sufficient for rosette formation, and that ERK1/2 signalling limits epidermal extrusion density. Furthermore, we find increased extrusion activity during starvation, and potential nutrient recycling via phagocytosis of extruded cells. Together, our findings indicate that epithelial cell extrusion has physiological roles in sea anemones and that its key hallmarks are likely evolutionarily ancient, predating the last common cnidarian-bilaterian ancestor.
    DOI:  https://doi.org/10.1038/s41467-026-74437-7
  18. Front Cell Infect Microbiol. 2026 ;16 1852001
      
    Keywords:  adaptation; cell death; cellular damage; host-pathogen interactions; microbial infections
    DOI:  https://doi.org/10.3389/fcimb.2026.1852001