Differential effect of nitric oxide on thrombospondin-1-, PDGF- and fibronectin-induced migration of vascular smooth muscle cells |
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| Authors: | Seymour Keri Han Xuan Sadowitz Benjamin Maier Kristopher G Gahtan Vivian |
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| Affiliation: | a Division of Vascular Surgery and Endovascular Services, SUNY Upstate Medical University, Syracuse, NY, USA
b Department of Veterans Affairs VA Healthcare Network Upstate New York at Syracuse, Syracuse, NY, USA |
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| Abstract: | BackgroundNeointimal hyperplasia involves the migration of medial vascular smooth muscle cells (VSMCs) in response to arterial injury. Thrombospondin-1 (TSP1), platelet-derived growth factor (PDGF), and fibronectin (Fn) induce VSMC migration. Nitric oxide (NO) limits VSMC migration. The hypothesis of this study is that NO would dose dependently inhibit TSP1-induced, PDGF-induced, and Fn-induced VSMC chemotaxis.MethodsVSMCs were pretreated with serum free media or the NO donors diethylenetriamine NONOate or S-nitroso-N-acetyl-D,L-penicillamine. Chemotaxis to TSP1, PDGF, or Fn was determined. Analysis of variance with post hoc testing was done. P values < .05 were considered significant.ResultsPDGF, TSP1, and Fn induced VSMC chemotaxis. NO donors inhibited chemotaxis of VSMCs to PDGF in a concentration-dependent manner. NO donors had a variable effect on TSP1-induced chemotaxis. NO donors did not inhibit Fn-induced chemotaxis.ConclusionThe complex interactions of these proteins in vivo will need to be considered when developing NO-dependent therapies for neointimal hyperplasia. |
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| Keywords: | Nitric oxide Thrombospondin-1 Migration Vascular smooth muscle cells Extracellular matrix PDGF |
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