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(Hypertension. 2001;38:1038.)
© 2001 American Heart Association, Inc.

Scientific Contributions

Cyclic Strain Increases Protease-Activated Receptor-1 Expression in Vascular Smooth Muscle Cells

Kytai T. Nguyen; Stacie R. Frye; Suzanne G. Eskin; Cam Patterson; Marschall S. Runge; Larry V. McIntire

From the Department of Bioengineering, Rice University (K.T.N., S.R.F., S.G.E., L.V.M.), Houston, Tex; and the Program in Molecular Cardiology, Department of Internal Medicine, University of North Carolina at Chapel Hill (C.P., M.S.R.).

Correspondence to Larry V. McIntire, PhD, Rice University, Department of Bioengineering MS 142, PO Box 1892, Houston, TX 77251-1892. E-mail mcintire{at}rice.edu

Abstract—— Cyclic strain regulates many vascular smooth muscle cell (VSMC) functions through changing gene expression. This study investigated the effects of cyclic strain on protease-activated receptor-1 (PAR-1) expression in VSMCs and the possible signaling pathways involved, on the basis of the hypothesis that cyclic strain would enhance PAR-1 expression, reflecting increased thrombin activity. Uniaxial cyclic strain (1 Hz, 20%) of cells cultured on elastic membranes induced a 2-fold increase in both PAR-1 mRNA and protein levels. Functional activity of PAR-1, as assessed by cell proliferation in response to thrombin, was also increased by cyclic strain. In addition, treatment of cells with antioxidants or an NADPH oxidase inhibitor blocked strain-induced PAR-1 expression. Preincubation of cells with protein kinase inhibitors (staurosporine or Ro 31-8220) enhanced strain-increased PAR-1 expression, whereas inhibitors of NO synthase, tyrosine kinase, and mitogen-activated protein kinases had no effect. Cyclic strain in the presence of basic fibroblast growth factor induced PAR-1 mRNA levels beyond the effect of cyclic strain alone, whereas no additive effect was observed between cyclic strain and platelet-derived growth factor-AB. Our findings that cyclic strain upregulates PAR-1 mRNA expression but that shear stress downregulates this gene in VSMCs provide an opportunity to elucidate signaling differences by which VSMCs respond to different mechanical forces.

Key Words: muscle, smooth, vascular • stress mechanical • gene expression • thrombin • protein kinases • oxidative stress

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