PlA polymorphism of integrin beta 3 differentially modulates cellular migration on extracellular matrix proteins

Arterioscler Thromb Vasc Biol. 2002 Dec 1;22(12):1984-9. doi: 10.1161/01.atv.0000043664.48689.7f.

Abstract

Objective: Cell migration is central to multiple physiological and pathologic processes and involves interactions between integrins on the cell surface and the extracellular matrix. The Leu33Pro (PlA) polymorphism of integrin beta3 has been reported to be associated with a greater rate of restenosis after angioplasty, a process involving endothelial and smooth muscle cell migration. We have addressed the possibility that the Leu33Pro polymorphism could modify the migratory behavior of Chinese hamster ovary (CHO) cells expressing the beta3-containing integrin complexes.

Methods and results: Haptotactic migratory responses of CHO alpha(IIb)beta3 cells to fibronectin and vitronectin were not statistically different between the Leu33 and Pro33 cells. However, CHO cells with the Pro33 (PlA2) polymorphism had an enhanced haptotactic migratory response to fibrinogen and von Willebrand Factor. This enhanced migration (1) could be blocked by the alpha(IIb)beta3-complex-specific neutralizing mAb 10E5, by 7E3, a neutralizing mAb specific for the beta3 integrin, and by the alpha(IIb)beta3-blocking peptide Integrilin; (2) was not observed with a CHO cell line expressing an activating beta3 Cys435 to Ala mutation; and (3) was attributable to increased activity of mitogen-activated protein kinase and cyclooxygenase. CHO cell lines expressing the Pro33 isoform of alpha(v)beta3 had an enhanced haptotactic migratory response to vitronectin and osteopontin but not fibrinogen.

Conclusions: The Leu33Pro polymorphism alters the migratory behavior of cells on extracellular matrix substrates, and the alpha subunit influences the substrate specificity of this genetic effect.

MeSH terms

  • Animals
  • CHO Cells / chemistry
  • CHO Cells / enzymology
  • CHO Cells / metabolism
  • Cell Adhesion / drug effects
  • Cell Adhesion / genetics
  • Cell Adhesion / physiology
  • Cell Line
  • Cell Movement / drug effects
  • Cell Movement / genetics*
  • Cricetinae
  • Cyclooxygenase 2
  • Diffusion Chambers, Culture
  • Enzyme Activation / physiology
  • Extracellular Matrix Proteins / physiology*
  • Fibrinogen / pharmacology
  • Integrin beta3 / biosynthesis
  • Integrin beta3 / genetics*
  • Integrin beta3 / physiology
  • Isoantigens / genetics
  • Isoenzymes / metabolism
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases / metabolism
  • Osteopontin
  • Platelet Glycoprotein GPIIb-IIIa Complex / biosynthesis
  • Polymorphism, Genetic*
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • Protein Isoforms / physiology
  • Sialoglycoproteins / pharmacology
  • Vitronectin / pharmacology
  • von Willebrand Factor / pharmacology

Substances

  • Extracellular Matrix Proteins
  • Integrin beta3
  • Isoantigens
  • Isoenzymes
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Protein Isoforms
  • Sialoglycoproteins
  • Vitronectin
  • von Willebrand Factor
  • Osteopontin
  • Fibrinogen
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases