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Projekt Druckansicht

Rolle von Alarminen aus neutrophilen Granulozyten in der Atherosklerose

Fachliche Zuordnung Kardiologie, Angiologie
Förderung Förderung von 2010 bis 2015
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 29385330
 
Erstellungsjahr 2015

Zusammenfassung der Projektergebnisse

While atherosclerosis is generally considered a monocyte-driven inflammation of the vessel wall, we here asked what the specific contribution of neutrophils, the most abundant circulating white blood cell subset in humans, towards atherosclerosis is. Using mouse models of neutropenia and neutrophilia we could evidence a direct relationship between circulating neutrophil counts and atherosclerosis lesion formation suggesting a causative role of 47mmune47phils in atherosclerosis. Mechanistically, we were able to identify CCR1, CCR2, CCR5, and CXCR2 as receptors guiding neutrophil recruitment into atherosclerotic lesions. The proatherogenic effect of neutrophils was found to rest upon their ability to release preformed chemotactic granule proteins. When interacting with host-DNA these granule proteins are recognized by plasmacytoid dendritic cells and hence unleash an interferon-alpha triggered inflammatory response. In addition, granule proteins immobilized on endothelial cells directly induce adhesion and recruitment of classical monocytes by strengthening integrin activation.

Projektbezogene Publikationen (Auswahl)

 
 

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