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Mediators of neutrophil recruitment in human abdominal aortic aneurysms

AIMS: 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. METHODS AND RESULTS: Conditioned media from...

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Autores principales: Houard, Xavier, Touat, Ziad, Ollivier, Véronique, Louedec, Liliane, Philippe, Monique, Sebbag, Uriel, Meilhac, Olivier, Rossignol, Patrick, Michel, Jean-Baptiste
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682614/
https://www.ncbi.nlm.nih.gov/pubmed/19201759
http://dx.doi.org/10.1093/cvr/cvp048
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author Houard, Xavier
Touat, Ziad
Ollivier, Véronique
Louedec, Liliane
Philippe, Monique
Sebbag, Uriel
Meilhac, Olivier
Rossignol, Patrick
Michel, Jean-Baptiste
author_facet Houard, Xavier
Touat, Ziad
Ollivier, Véronique
Louedec, Liliane
Philippe, Monique
Sebbag, Uriel
Meilhac, Olivier
Rossignol, Patrick
Michel, Jean-Baptiste
author_sort Houard, Xavier
collection PubMed
description AIMS: 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. METHODS AND RESULTS: Conditioned media from luminal, intermediate, and abluminal layers of 29 human ILTs were analysed for neutrophil markers [elastase/α(1)-antitrypsin and MMP9/NGAL complexes, myeloperoxidase (MPO), and α-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. CONCLUSION: 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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spelling pubmed-26826142009-05-15 Mediators of neutrophil recruitment in human abdominal aortic aneurysms Houard, Xavier Touat, Ziad Ollivier, Véronique Louedec, Liliane Philippe, Monique Sebbag, Uriel Meilhac, Olivier Rossignol, Patrick Michel, Jean-Baptiste Cardiovasc Res Original Articles AIMS: 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. METHODS AND RESULTS: Conditioned media from luminal, intermediate, and abluminal layers of 29 human ILTs were analysed for neutrophil markers [elastase/α(1)-antitrypsin and MMP9/NGAL complexes, myeloperoxidase (MPO), and α-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. CONCLUSION: 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. Oxford University Press 2009-06-01 2009-02-05 /pmc/articles/PMC2682614/ /pubmed/19201759 http://dx.doi.org/10.1093/cvr/cvp048 Text en Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2009. For permissions please email: journals.permissions@oxfordjournals.org.
spellingShingle Original Articles
Houard, Xavier
Touat, Ziad
Ollivier, Véronique
Louedec, Liliane
Philippe, Monique
Sebbag, Uriel
Meilhac, Olivier
Rossignol, Patrick
Michel, Jean-Baptiste
Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title_full Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title_fullStr Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title_full_unstemmed Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title_short Mediators of neutrophil recruitment in human abdominal aortic aneurysms
title_sort mediators of neutrophil recruitment in human abdominal aortic aneurysms
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682614/
https://www.ncbi.nlm.nih.gov/pubmed/19201759
http://dx.doi.org/10.1093/cvr/cvp048
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