4.7 Article

Mediators of neutrophil recruitment in human abdominal aortic aneurysms

期刊

CARDIOVASCULAR RESEARCH
卷 82, 期 3, 页码 532-541

出版社

OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvp048

关键词

Intraluminal thrombus; Interleukin-8; RANTES; PF4; MMP9; NGAL; MPO; Elastase/alpha(1)-antitrypsin; alpha-Defensins

资金

  1. Fondation Lefoulon-Delalande
  2. Fondation pour la Recherche Me dicale
  3. Fondation de France
  4. Leducq Foundation
  5. Fondation pour la Recherche Medicale
  6. FP-7 European Union integrated project 'Fighting Aneurysmal Disease' (FAD)
  7. INSERM

向作者/读者索取更多资源

Neutrophils/platelet interactions are involved in abdominal aortic aneurysm (AAA). The intraluminal thrombus (ILT) is a human model of platelet/neutrophil interactions. The present study focused on mediators involved in neutrophil recruitment in AAA. Conditioned media from luminal, intermediate, and abluminal layers of 29 human ILTs were analysed for neutrophil markers [elastase/alpha(1)-antitrypsin and MMP9/NGAL complexes, myeloperoxidase (MPO), and alpha-defensin peptides], RANTES, platelet factor 4 (PF4), and interleukin-8 (IL-8). Their time-dependent release into serum from clots generated in vitro and their plasma concentrations in AAA patients and controls were determined. Immunohistochemistry for neutrophils, platelets, IL-8, PF4, and RANTES on AAA sections was performed; and molecules involved in ILT neutrophil chemotactic function were analysed in vitro. Neutrophils and platelets colocalized in the luminal layer of the thrombus. Consistently, neutrophil markers and platelet-derived RANTES and PF4 were released predominantly by the luminal thrombus pole, where their concentrations were significantly correlated. The luminal ILT layer was also the main source of IL-8, whose immunostaining colocalized with neutrophils. All were also released time dependently from clots and were increased in plasma of AAA patients. Luminal ILT layers displayed potent neutrophil chemotactic activity in vitro, which was inhibited by RANTES- and IL-8-blocking antibodies as well as by reparixin, an antagonist of the IL-8 receptors CXCR1 and CXCR2. Taken together, these results suggest that platelet-derived RANTES and neutrophil-derived IL-8 are involved in attracting neutrophils to the luminal layer of AAA ILT.

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