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- W4207024195 endingPage "102515" @default.
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- W4207024195 abstract "Monocyte-induced endothelial cell inflammation is associated with multiple pathological conditions, and extracellular vesicles (EVs) are essential nanosized components of intercellular communication. EVs derived from endotoxin-stimulated monocytes were previously shown to carry pro-inflammatory proteins and RNAs. The role of glucose transporter-1 (GLUT-1) and glycan features in monocyte-derived EV-induced endothelial cell inflammation remains largely unexplored. This study demonstrates that EVs derived from endotoxin-stimulated monocytes activate inflammatory pathways in endothelial cells, which are partially attributed to GLUT-1. Alterations in glycan features and increased levels of GLUT-1 were observed in EVs derived from endotoxin-stimulated monocytes. Notably, inhibition of EV-associated GLUT-1, through the use of fasentin, suppressed EV-induced inflammatory cytokines in recipient endothelial cells." @default.
- W4207024195 created "2022-01-26" @default.
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- W4207024195 date "2022-06-01" @default.
- W4207024195 modified "2023-10-01" @default.
- W4207024195 title "Extracellular vesicle glucose transporter-1 and glycan features in monocyte-endothelial inflammatory interactions" @default.
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- W4207024195 doi "https://doi.org/10.1016/j.nano.2022.102515" @default.
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