Neutrophil microvesicles drive atherosclerosis by delivering miR-155 to atheroprone endothelium

中性粒细胞微囊泡通过将 miR-155 递送至易发生动脉粥样硬化的内皮细胞来促进动脉粥样硬化的发生。

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作者:Ingrid Gomez,Ben Ward,Celine Souilhol,Chiara Recarti,Mark Ariaans,Jessica Johnston,Amanda Burnett,Marwa Mahmoud,Le Anh Luong,Laura West,Merete Long,Sion Parry,Rachel Woods,Carl Hulston,Birke Benedikter,Chiara Niespolo,Rohit Bazaz,Sheila Francis,Endre Kiss-Toth,Marc van Zandvoort,Andreas Schober,Paul Hellewell,Paul C Evans ,Victoria Ridger

Abstract

Neutrophils are implicated in the pathogenesis of atherosclerosis but are seldom detected in atherosclerotic plaques. We investigated whether neutrophil-derived microvesicles may influence arterial pathophysiology. Here we report that levels of circulating neutrophil microvesicles are enhanced by exposure to a high fat diet, a known risk factor for atherosclerosis. Neutrophil microvesicles accumulate at disease-prone regions of arteries exposed to disturbed flow patterns, and promote vascular inflammation and atherosclerosis in a murine model. Using cultured endothelial cells exposed to disturbed flow, we demonstrate that neutrophil microvesicles promote inflammatory gene expression by delivering miR-155, enhancing NF-κB activation. Similarly, neutrophil microvesicles increase miR-155 and enhance NF-κB at disease-prone sites of disturbed flow in vivo. Enhancement of atherosclerotic plaque formation and increase in macrophage content by neutrophil microvesicles is dependent on miR-155. We conclude that neutrophils contribute to vascular inflammation and atherogenesis through delivery of microvesicles carrying miR-155 to disease-prone regions.

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