Integrin-linked kinase functions as a downstream signal of platelet-derived growth factor to regulate actin polymerization and vascular smooth muscle cell migration |
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Authors: | Mitra Esfandiarei Sahar Abdoli Yazdi Virginia Gray Shoukat Dedhar Cornelis van Breemen |
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Affiliation: | (1) Department of Anesthesiology, Pharmacology, and Therapeutics, University of British Columbia, Child & Family Research Institute, 950 West 28th Avenue, Vancouver, BC, V5Z 4H4, Canada;(2) Department of Cancer Genetics, British Columbia Cancer Research Centre, University of British Columbia, 675 West 10th Avenue, Vancouver, BC, V5Z 1L3, Canada |
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Abstract: | Background Vascular smooth muscle cell migration and accumulation in response to growth factors extensively contribute to the development of intimal thickening within the vessel wall. Cumulative evidence has shown that actin cytoskeleton polymerization and rearrangement are critical steps during cellular spreading and migration. Integrin-linked kinase, an intracellular serine/threonine kinase, is a cytoplasmic interactor of integrin beta-1 and beta-3 receptors regulating cell-cell and/or cell-extracellular matrix interaction, cell contraction, extracellular matrix modification, and cell spreading and migration in response to various stimuli. However, the regulatory role of ILK during vascular smooth muscle cell migration and the importance of integrin signaling in occlusive vascular diseases are not yet fully elucidated. |
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