Flow Perturbation Mediates Neutrophil Recruitment and Potentiates Endothelial Injury via TLR2 in Mice

Rationale:Superficial erosion currently causes up to a third of acute coronary syndromes; yet, we lack understanding of its mechanisms. Thrombi because of superficial intimal erosion characteristically complicate matrix-rich atheromata in regions of flow perturbation.Objective:This study tested in v...

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Veröffentlicht in:Circulation research 2017-06, Vol.121 (1), p.31-42
Hauptverfasser: Franck Grégory, Mawson, Thomas, Sausen Grasiele, Salinas, Manuel, Masson, Gustavo Santos, Cole, Andrew, Beltrami-Moreira, Marina, Chatzizisis Yiannis, Thibault, Quillard, Tesmenitsky Yevgenia, Shvartz Eugenia, Sukhova, Galina K, Swirski, Filip K, Nahrendorf Matthias, Aikawa, Elena, Croce, Kevin J, Libby, Peter
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Sprache:eng
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Zusammenfassung:Rationale:Superficial erosion currently causes up to a third of acute coronary syndromes; yet, we lack understanding of its mechanisms. Thrombi because of superficial intimal erosion characteristically complicate matrix-rich atheromata in regions of flow perturbation.Objective:This study tested in vivo the involvement of disturbed flow and of neutrophils, hyaluronan, and Toll-like receptor 2 ligation in superficial intimal injury, a process implicated in superficial erosion.Methods and Results:In mouse carotid arteries with established intimal lesions tailored to resemble the substrate of human eroded plaques, acute flow perturbation promoted downstream endothelial cell activation, neutrophil accumulation, endothelial cell death and desquamation, and mural thrombosis. Neutrophil loss-of-function limited these findings. Toll-like receptor 2 agonism activated luminal endothelial cells, and deficiency of this innate immune receptor decreased intimal neutrophil adherence in regions of local flow disturbance, reducing endothelial cell injury and local thrombosis (P
ISSN:0009-7330
1524-4571
DOI:10.1161/CIRCRESAHA.117.310694