Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells

In addition to the induction of cell proliferation and migration, bradykinin (BK) can increase c-fos mRNA expression, activate ERK 1/2 and generate reactive oxygen species (ROS) in vascular smooth muscle cells (VSMC). It is not known, however, whether BK can induce cellular proliferation and extrace...

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Autores principales: VELARDE,VICTORIA, DE LA CERDA,PAULA M, DUARTE,CLAUDIA, ARANCIBIA,FRANCISCA, ABBOTT,EDUARDO, GONZÁLEZ,ALEJANDRO, MORENO,FRANCESCA, JAFFA,AYAD A
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2004
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000300007
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spelling oai:scielo:S0716-976020040003000072005-03-14Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cellsVELARDE,VICTORIADE LA CERDA,PAULA MDUARTE,CLAUDIAARANCIBIA,FRANCISCAABBOTT,EDUARDOGONZÁLEZ,ALEJANDROMORENO,FRANCESCAJAFFA,AYAD A bradykinin, antioxidants migration signal transduction reactive oxygen species In addition to the induction of cell proliferation and migration, bradykinin (BK) can increase c-fos mRNA expression, activate ERK 1/2 and generate reactive oxygen species (ROS) in vascular smooth muscle cells (VSMC). It is not known, however, whether BK can induce cellular proliferation and extracellular matrix production via redox-sensitive signaling pathways. We investigated the role(s) of ROS in proliferation, migration and collagen synthesis induced by BK in VSMC derived from Sprague Dawley rat aorta. BK (10 nM) increased VSMC proliferation by 30 % (n=5); this proliferation was inhibited by the antioxidants N-acetylcysteine (20 mM) and a-lipoic acid (LA, 250 mM). In addition, BK induced an increase in cell migration and in collagen levels that were blocked by LA. ROS production induced by BK (n=10) was significantly inhibited by bisindolylmaleimide (4mM) and by PD98059 (40mM). These results suggest that: 1) ROS participate in the mechanism(s) used by bradykinin to induce cellular proliferation; 2) bradykinin induces ROS generation through a pathway that involves the kinases PKC and MEK; and 3) ROS participate in the pathways mediating cell migration and the production of collagen as a response to treatment with bradykinin. To our knowledge, this is the first report describing mechanisms to explain the participation of ROS in the cellular proliferation and extracellular matrix pathway regulated by BKinfo:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.37 n.3 20042004-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000300007en10.4067/S0716-97602004000300007
institution Scielo Chile
collection Scielo Chile
language English
topic bradykinin, antioxidants
migration
signal transduction
reactive oxygen species
spellingShingle bradykinin, antioxidants
migration
signal transduction
reactive oxygen species
VELARDE,VICTORIA
DE LA CERDA,PAULA M
DUARTE,CLAUDIA
ARANCIBIA,FRANCISCA
ABBOTT,EDUARDO
GONZÁLEZ,ALEJANDRO
MORENO,FRANCESCA
JAFFA,AYAD A
Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
description In addition to the induction of cell proliferation and migration, bradykinin (BK) can increase c-fos mRNA expression, activate ERK 1/2 and generate reactive oxygen species (ROS) in vascular smooth muscle cells (VSMC). It is not known, however, whether BK can induce cellular proliferation and extracellular matrix production via redox-sensitive signaling pathways. We investigated the role(s) of ROS in proliferation, migration and collagen synthesis induced by BK in VSMC derived from Sprague Dawley rat aorta. BK (10 nM) increased VSMC proliferation by 30 % (n=5); this proliferation was inhibited by the antioxidants N-acetylcysteine (20 mM) and a-lipoic acid (LA, 250 mM). In addition, BK induced an increase in cell migration and in collagen levels that were blocked by LA. ROS production induced by BK (n=10) was significantly inhibited by bisindolylmaleimide (4mM) and by PD98059 (40mM). These results suggest that: 1) ROS participate in the mechanism(s) used by bradykinin to induce cellular proliferation; 2) bradykinin induces ROS generation through a pathway that involves the kinases PKC and MEK; and 3) ROS participate in the pathways mediating cell migration and the production of collagen as a response to treatment with bradykinin. To our knowledge, this is the first report describing mechanisms to explain the participation of ROS in the cellular proliferation and extracellular matrix pathway regulated by BK
author VELARDE,VICTORIA
DE LA CERDA,PAULA M
DUARTE,CLAUDIA
ARANCIBIA,FRANCISCA
ABBOTT,EDUARDO
GONZÁLEZ,ALEJANDRO
MORENO,FRANCESCA
JAFFA,AYAD A
author_facet VELARDE,VICTORIA
DE LA CERDA,PAULA M
DUARTE,CLAUDIA
ARANCIBIA,FRANCISCA
ABBOTT,EDUARDO
GONZÁLEZ,ALEJANDRO
MORENO,FRANCESCA
JAFFA,AYAD A
author_sort VELARDE,VICTORIA
title Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
title_short Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
title_full Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
title_fullStr Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
title_full_unstemmed Role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
title_sort role of reactive oxygen species in bradykinin-induced proliferation of vascular smooth muscle cells
publisher Sociedad de Biología de Chile
publishDate 2004
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000300007
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