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Am J Physiol Cell Physiol 290: C972-C980, 2006. First published November 9, 2005; doi:10.1152/ajpcell.00136.2005
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VASCULAR BIOLOGY

Modulation of {alpha}7-integrin-mediated adhesion and expression by platelet-derived growth factor in vascular smooth muscle cells

Jun-Tzu Chao,1 Luis A. Martinez-Lemus,1 Stephen J. Kaufman,2 Gerald A. Meininger,1 Kenneth S. Ramos,3 and Emily Wilson1

1Division of Vascular Biology, Cardiovascular Research Institute, The Texas A&M University System Health Science Center, College Station, Texas; 2Department of Cell and Structural Biology, University of Illinois, Urbana, Illinois; and 3Department of Biochemistry and Molecular Biology, University of Louisville, Louisville, Kentucky

Submitted 23 March 2005 ; accepted in final form 2 November 2005

We showed previously that the expression of {alpha}7-integrin in aortic vascular smooth muscle cells (VSMC) is enhanced in a rat model of atherosclerosis. In the present study, we investigated the effects of platelet-derived growth factor (PDGF) on {alpha}7-integrin expression and VSMC adhesion and migration. Expression of the {alpha}7-integrin gene was determined by real-time RT-PCR, whereas protein levels were determined by fluorescence-activated cell sorting analysis. PDGF increased {alpha}7 cell surface protein expression (12 and 24 h: 3.3 ± 0.8- and 3.6 ± 0.4-fold, P < 0.05 vs. control) and mRNA levels (24 h: 3.1-fold, P < 0.05 vs. control) in a time-dependent manner. Actinomycin D and cycloheximide attenuated PDGF-induced increases in {alpha}7-integrin, indicating the involvement of de novo mRNA and protein synthesis. Treatment with the MAPK inhibitors PD-98059, SP-600125, and SB-203580 attenuated PDGF-induced increases in mRNA. In contrast, PD-98059 and SP-600125, but not SB-203580, attenuated PDGF-induced increases in cell surface protein levels. PDGF-treated VSMC adhered to laminin more efficiently (42 ± 6% increase, P < 0.01), and this increase was partially inhibited by anti-{alpha}7-integrin function-blocking antibody. However, PDGF did not alter migration on laminin, and there was no effect of the anti-{alpha}7-integrin function-blocking antibody on basal or PDGF-stimulated migration. Immunofluorescence imaging revealed an increase in {alpha}7-integrin distribution along the stress fibers. Together, these observations indicate that PDGF enhances {alpha}7-integrin expression in VSMC and promotes {alpha}7-integrin-mediated adhesion to laminin.

vascular injury; laminin; mitogen-activated protein kinase



Address for reprint requests and other correspondence: E. Wilson, Cardiovascular Research Institute, The Texas A&M Univ. System Health Science Center, 336 Joe Reynolds Medical Bldg., College Station, TX 77843 (e-mail: emilyw{at}tamu.edu)




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