Article en vedette : Impact des vésicules apoptotiques de type exosome sur la fonction des cellules endothéliales

Le PRDTC tient à féliciter Marie-Josée Hébert, Francis Migneault, Mélanie Dieudé, Julie Turgeon et tous les autres collaborateurs qui ont travaillé sur l’article intitulé Apoptotic exosome‑like vesicles regulate endothelial gene expression, inflammatory signaling, and function through the NF‑κB signaling pathway, récemment publié dans la revue Nature – Scientific Reports!

Un bel effort d’équipe sur l’impact des vésicules apoptotiques de type exosome sur la fonction des cellules endothéliales.

Résumé (en anglais)

Persistent endothelial injury promotes maladaptive responses by favoring the release of factors leading to perturbation in vascular homeostasis and tissue architecture. Caspase-3 dependent death of microvascular endothelial cells leads to the release of unique apoptotic exosome-like vesicles (ApoExo). Here, we evaluate the impact of ApoExo on endothelial gene expression and function in the context of a pro-apoptotic stimulus. Endothelial cells exposed to ApoExo differentially express genes involved in cell death, inflammation, differentiation, and cell movement. Endothelial cells exposed to ApoExo showed inhibition of apoptosis, improved wound closure along with reduced angiogenic activity and reduced expression of endothelial markers consistent with the first phase of endothelial-to-mesenchymal transition (endoMT). ApoExo interaction with endothelial cells also led to NF-κB activation. NF-κB is known to participate in endothelial dysfunction in numerous diseases. Silencing NF-κB reversed the anti-apoptotic effect and the pro-migratory state and prevented angiostatic properties and CD31 downregulation in endothelial cells exposed to ApoExo. This study identifies vascular injury-derived extracellular vesicles (ApoExo) as novel drivers of NF-κB activation in endothelial cells and demonstrates the pivotal role of this signaling pathway in coordinating ApoExo-induced functional changes in endothelial cells. Hence, targeting ApoExo-mediated NF-κB activation in endothelial cells opens new avenues to prevent endothelial dysfunction.

Vous pouvez lire l’article ici (en anglais).