Journal
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 25, Issue 10, Pages 2088-2093Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.ATV.0000183607.50230.9f
Keywords
C-reactive protein; endothelial cells; NF-kappa B; PAI-1; Rho/Rho-kinase
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Objective - Rho/Rho-kinase pathway plays pivotal roles in cardiovascular diseases including arteriosclerosis and hypertension. Recently it has become evident that C-reactive protein (CRP), a powerful marker for cardiovascular events, has direct proatherothrombotic effects on vascular cells. However, its molecular mechanism has not been fully investigated. We examined the involvement of Rho/Rho-kinase signaling in CRP-induced plasminogen activator inhibitor-1 (PAI-1) expression in bovine aortic endothelial cells (BAECs). Methods and Results - PAI-1 expression was determined by Western blotting. RhoA activation was determined by an affinity pull-down assay using Rho-binding fragment of rhotekin. NF-kappa B activity was determined using the luciferase reporter gene. Incubation of BAECs with human recombinant CRP ( >= 25 mu g/mL) induced a significant increase in PAI-1 expression. Stimulation of BAECs with CRP significantly increased RhoA activation. Pretreatment with TAT-C3 ( a membrane-permeable RhoA inhibitor) and Y-27632 ( Rho-kinase inhibitor) significantly inhibited CRP-induced PAI-1 expression. NF-kappa B activity was markedly enhanced by CRP and pretreatment with Y- 27632 inhibited its activation. Parthenolide, SN50, and BAY 11-7082 (NF-kappa B inhibitors) significantly blocked CRP-mediated PAI-1 expression. Conclusions - These data suggested that CRP activates Rho/Rho-kinase signaling, which in turn activates NF-kappa B activity, resulting in PAI-1 expression in BAEC. These observations provide evidence for the possible involvement of Rho/Rho-kinase signaling in CRP-induced atherothrombogenesis.
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