Cargando…

Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion

Recent evidence indicates novel role for matrix metalloproteinases (MMPs), in particular gelatinase A (MMP-2), in the regulation of vascular biology that are unrelated to their well-known proteolytic breakdown of matrix proteins. We have previously reported that MMP-2 can modulate vascular reactivit...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernandez-Patron, Carlos, Zouki, Christine, Whittal, Randy M., Chan, John S.D., Davidge, Sandra T., Filep, János G.
Formato: Texto
Lenguaje:English
Publicado: Biological Procedures Online 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC145555/
https://www.ncbi.nlm.nih.gov/pubmed/12734570
http://dx.doi.org/10.1251/bpo32
_version_ 1782120611058810880
author Fernandez-Patron, Carlos
Zouki, Christine
Whittal, Randy M.
Chan, John S.D.
Davidge, Sandra T.
Filep, János G.
author_facet Fernandez-Patron, Carlos
Zouki, Christine
Whittal, Randy M.
Chan, John S.D.
Davidge, Sandra T.
Filep, János G.
author_sort Fernandez-Patron, Carlos
collection PubMed
description Recent evidence indicates novel role for matrix metalloproteinases (MMPs), in particular gelatinase A (MMP-2), in the regulation of vascular biology that are unrelated to their well-known proteolytic breakdown of matrix proteins. We have previously reported that MMP-2 can modulate vascular reactivity by cleavage of the Gly32-Leu33 bound in big endothelin-1 (ET-1) yielding a novel vasoactive peptide ET-1[1-32]. These studies were conducted to investigate whether gelatinolytic MMPs could affect neutrophil-endothelial cell attachment. ET-1[1-32] produced by MMP-2 up-regulated CD11b/CD18 expression on human neutrophils, thereby promoted their adhesion to cultured endothelial cells. ET-1[1-32] evoked release of gelatinase B (MMP-9), which in turn cleaved big ET-1 to yield ET-1[1-32], thus revealing a self-amplifying loop for ET-1[1-32] generation. ET-1[1-32] was rather resistant to cleavage by neutrophil proteases and further metabolism of ET-1[1-32] was not a prerequisite for its biological actions on neutrophils. The neutrophil responses to ET-1[1-32] were mediated via activation of ET(A)receptors through activation of the Ras/Raf-1/MEK/ERK signaling pathway. These results suggest a novel role for gelatinase A and B in the regulation of neutrophil functions and their interactions with endothelial cells. Here we describe the methods in detail as they relate to our previously published work.
format Text
id pubmed-145555
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher Biological Procedures Online
record_format MEDLINE/PubMed
spelling pubmed-1455552003-04-15 Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion Fernandez-Patron, Carlos Zouki, Christine Whittal, Randy M. Chan, John S.D. Davidge, Sandra T. Filep, János G. Biol Proced Online Research Article Recent evidence indicates novel role for matrix metalloproteinases (MMPs), in particular gelatinase A (MMP-2), in the regulation of vascular biology that are unrelated to their well-known proteolytic breakdown of matrix proteins. We have previously reported that MMP-2 can modulate vascular reactivity by cleavage of the Gly32-Leu33 bound in big endothelin-1 (ET-1) yielding a novel vasoactive peptide ET-1[1-32]. These studies were conducted to investigate whether gelatinolytic MMPs could affect neutrophil-endothelial cell attachment. ET-1[1-32] produced by MMP-2 up-regulated CD11b/CD18 expression on human neutrophils, thereby promoted their adhesion to cultured endothelial cells. ET-1[1-32] evoked release of gelatinase B (MMP-9), which in turn cleaved big ET-1 to yield ET-1[1-32], thus revealing a self-amplifying loop for ET-1[1-32] generation. ET-1[1-32] was rather resistant to cleavage by neutrophil proteases and further metabolism of ET-1[1-32] was not a prerequisite for its biological actions on neutrophils. The neutrophil responses to ET-1[1-32] were mediated via activation of ET(A)receptors through activation of the Ras/Raf-1/MEK/ERK signaling pathway. These results suggest a novel role for gelatinase A and B in the regulation of neutrophil functions and their interactions with endothelial cells. Here we describe the methods in detail as they relate to our previously published work. Biological Procedures Online 2002-10-28 /pmc/articles/PMC145555/ /pubmed/12734570 http://dx.doi.org/10.1251/bpo32 Text en Copyright © October 10, 2002, C Fernandez-Patron et al. Published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted.
spellingShingle Research Article
Fernandez-Patron, Carlos
Zouki, Christine
Whittal, Randy M.
Chan, John S.D.
Davidge, Sandra T.
Filep, János G.
Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title_full Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title_fullStr Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title_full_unstemmed Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title_short Methods for Analysis of Matrix Metalloproteinase Regulation of Neutrophil-Endothelial Cell Adhesion
title_sort methods for analysis of matrix metalloproteinase regulation of neutrophil-endothelial cell adhesion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC145555/
https://www.ncbi.nlm.nih.gov/pubmed/12734570
http://dx.doi.org/10.1251/bpo32
work_keys_str_mv AT fernandezpatroncarlos methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion
AT zoukichristine methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion
AT whittalrandym methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion
AT chanjohnsd methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion
AT davidgesandrat methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion
AT filepjanosg methodsforanalysisofmatrixmetalloproteinaseregulationofneutrophilendothelialcelladhesion