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Vesicular transplantation of gasdermin pores propagates pyroptosis

GSE277224 Mus musculus Expression profiling by high throughput sequencing 6 samples Submitted 2025/01/07 Platform GPL24247
Summary
Pyroptosis—inflammatory cell death mediated by gasdermins (GSDM)—plays crucial roles in antimicrobial defense and inflammatory diseases. Pyroptosis results in the release of proinflammatory molecules, including damage-associated molecular patterns (DAMPs). However, our understanding of the consequences of pyroptosis—especially beyond IL-1 cytokines and DAMPs—that govern inflammation is limited. Here, we show intercellular propagation of pyroptosis from dying cells to bystander cells in vitro and in vivo. We identified extracellular vesicles (EVs) released by pyroptosing cells as the propagator of lytic death to naïve cells, triggering inflammatory responses and tissue damage. Remarkably, DNA-PAINT super-resolution and immunoelectron microscopical analyses revealed the presence of GSDMD nanostructures, such as pores, on EVs released by pyroptotic cells. Importantly, the transplantation of these GSDMD pores on adjacent cells’ plasma membrane by EVs causes cell-extrinsic lysis of bystanders. Overall, our findings demonstrate that cell-to-cell vesicular transplantation of GSDMD pores disseminates pyroptosis, revealing a domino-like effect shaping disease-associated bystander cell death.
Published in
Transplantation of gasdermin pores by extracellular vesicles propagates pyroptosis to bystander cells
Wright SS, Kumari P, Fraile-Ágreda V et al. · Cell 2025 · PMID 39742811 · doi:10.1016/j.cell.2024.11.018
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Also filed as BioProject PRJNA1161397 and SRA study SRP532804. Searching any of these in the dataset finder brings you back here.

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