Transplantation of gasdermin pores by extracellular vesicles propagates pyroptosis to bystander cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39742811.
- Also identified by DOI 10.1016/j.cell.2024.11.018 and PMC identifier 12272064.
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Abstract
Pyroptosis mediated by gasdermins (GSDMs) plays crucial roles in infection and inflammation. Pyroptosis triggers the release of inflammatory molecules, including damage-associated molecular patterns (DAMPs). However, the consequences of pyroptosis-especially beyond interleukin (IL)-1 cytokines and DAMPs-that govern inflammation are poorly defined. 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 pyroptotic cells as the propagator of lytic death to naive cells, promoting inflammation. DNA-PAINT super-resolution and immunoelectron microscopy revealed GSDMD pore structures on EVs released by pyroptotic cells. Importantly, pyroptotic EVs transplant GSDMD pores on the plasma membrane of bystander cells and kill them. Overall, we demonstrate that cell-to-cell vesicular transplantation of GSDMD pores disseminates pyroptosis, revealing a domino-like effect governing disease-associated bystander cell death.
Medical subject headings
- Pyroptosis
- Extracellular Vesicles
- Phosphate-Binding Proteins
- Bystander Effect
- Intracellular Signaling Peptides and Proteins