Urokinase-type plasminogen activator receptor (upar) ligation induces a raft-localized integrin signaling switch that mediates the hypermotile phenotype of fibrotic fibroblasts

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Abstract

Background: Fibroblasts from patients with idiopathic pulmonary fibrosis (IPF) overexpress the urokinase-type plasminogen activator receptor (uPAR) and are hypermotile. Results: uPAR ligation increases fibroblast motility by localizing α5β1 integrin-Fyn signaling complexes to lipid rafts. Conclusion: The hypermotile phenotype of IPF fibroblasts is due to lipid raft-localized uPAR-integrin-Fyn signaling complexes. Significance: These unique lipid raft signals may be therapeutic targets for IPF. © 2014 by The American Society for Biochemistry and Molecular Biology, Inc.

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Grove, L. M., Southern, B. D., Jin, T. H., White, K. E., Paruchuri, S., Harel, E., … Olman, M. A. (2014). Urokinase-type plasminogen activator receptor (upar) ligation induces a raft-localized integrin signaling switch that mediates the hypermotile phenotype of fibrotic fibroblasts. Journal of Biological Chemistry, 289(18), 12791–12804. https://doi.org/10.1074/jbc.M113.498576

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