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Reactive oxygen species-sensitive p38 MAPK controls thrombin-induced migration of vascular smooth muscle cells

  • Zhongbiao Wang(corresponding author)
    ,
  • Manuel R. Castresana
    ,
  • Walter H. Newman
*Corresponding author for this work
  • Mercer University
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Thrombin has been implicated in the development of atherosclerosis and restenosis, in which migration of vascular smooth muscle cells (VSMC) is a crucial event. Thrombin-stimulated VSMC migration is associated with increased generation of reactive oxygen species (ROS), activation of mitogen-activated protein kinases (MAPKs), and production of growth factors and chemoattractants. In this study, we examined the interrelation of these signals to determine the pathway controlling thrombin-directed migration of human VSMC. Our results show that thrombin stimulated the production of ROS and activation of p38 MAPK. ROS were required for thrombin-induced VSMC migration since both generation of ROS and cell migration were significantly attenuated by inhibitors of NAD(P)H oxidase, diphenyleneiodonium (DPI) and apocynin (Apo.), and by the hydrogen peroxide scavenger, catalase (Cat.). Activation of p38 MAPK by thrombin was inhibited by DPI, Apo. and Cat., indicating ROS are used as messengers for activating this kinase. p38 MAPK is an important step since SB 203580, a selective inhibitor of p38 MAPK, suppressed the cell migration induced by thrombin. Furthermore, thrombin increased the expression of vascular endothelial growth factor (VEGF), a chemoattractant for VSMC, and this expression was inhibited by DPI, Apo., Cat. and SB 203580. Addition of anti-VEGF antibody significantly attenuated thrombin-induced migration. Collectively, the data presented here show that thrombin has stimulated VSMC migration and VEGF expression through an ROS-sensitive p38 MAPK pathway. VEGF synthesized and released by the cell served as a secondary mediator in thrombin-directed migration.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 49-56 (8 pages)

Journal (Volume, Issue Number)

Journal of molecular and cellular cardiology (Volume 36, Issue 1)

Publication milestones

  • Published - 01/2004

Publication status

Published - 01/2004

ISSN

0022-2828

Publication IDs

  • Scopus: 0346374651
  • PubMed: 14734047

Publication metrics

Metrics

Scopus
citations
SciVal
citations
64
SciVal
FWCI
2.13
SciVal
Author count
3
SciVal
Paper percentile
89
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1

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Citation count
72
Captures
10

Funding Details

This work was supported in part by a grant from the MedCen Foundation and the Clinical Research Center of the Medical Center of Central Georgia. We thank Benjamin Parrish Mitchell for his effort in the cell culture.
FundersFunding numbers
Medical Center of Central Georgia
-
Medcen Community Health Foundation
-