Adenoviral expression of a urokinase receptor-targeted protease inhibitor inhibits neointima formation in murine and human blood vessels

Circulation. 2001 Jan 30;103(4):562-9. doi: 10.1161/01.cir.103.4.562.

Abstract

Background: Smooth muscle cell migration, in addition to proliferation, contributes to a large extent to the neointima formed in humans after balloon angioplasty or bypass surgery. Plasminogen activator/plasmin-mediated proteolysis is an important mediator of this smooth muscle cell migration. Here, we report the construction of a novel hybrid protein designed to inhibit the activity of cell surface-bound plasmin, which cannot be inhibited by its natural inhibitors, such as alpha(2)-antiplasmin. This hybrid protein, consisting of the receptor-binding amino-terminal fragment of uPA (ATF), linked to the potent protease inhibitor bovine pancreas trypsin inhibitor (BPTI), can inhibit plasmin activity at the cell surface.

Methods and results: The effect of adenovirus-mediated ATF.BPTI expression on neointima formation was tested in human saphenous vein organ cultures. Infection of human saphenous vein segments with Ad.CMV.ATF.BPTI (5x10(9) pfu/mL) resulted in 87.5+/-3.8% (mean+/-SEM, n=10) inhibition of neointima formation after 5 weeks, whereas Ad.CMV.ATF or Ad.CMV.BPTI virus had only minimal or no effect on neointima formation. The efficacy of ATF.BPTI in vivo was demonstrated in a murine model for neointima formation. Neointima formation in the femoral artery of mice, induced by placement of a polyethylene cuff, was strongly inhibited (93.9+/-2%) after infection with Ad.CMV.mATF.BPTI, a variant of ATF.BPTI able to bind specifically to murine uPA receptor; Ad.CMV.mATF and Ad.CMV.BPTI had no significant effect.

Conclusions: These data provide evidence that adenoviral transfer of a hybrid protein that binds selectively to the uPA receptor and inhibits plasmin activity directly on the cell surface is a powerful approach to inhibiting neointima formation and restenosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Aprotinin / genetics
  • Aprotinin / physiology*
  • Blood Vessels / physiology*
  • CHO Cells
  • Cattle
  • Cricetinae
  • Femoral Artery / growth & development
  • Femoral Artery / injuries
  • Femoral Vein / cytology
  • Femoral Vein / metabolism
  • Fibrinolysin / metabolism
  • Gene Expression
  • Genetic Vectors / genetics
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / metabolism
  • Organ Culture Techniques
  • Peptide Fragments / genetics
  • Peptide Fragments / physiology
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / physiology
  • Saphenous Vein / cytology
  • Transfection
  • Tunica Intima / growth & development*
  • Urokinase-Type Plasminogen Activator / chemistry
  • Urokinase-Type Plasminogen Activator / genetics
  • Urokinase-Type Plasminogen Activator / physiology*

Substances

  • Peptide Fragments
  • Recombinant Fusion Proteins
  • Aprotinin
  • Fibrinolysin
  • Urokinase-Type Plasminogen Activator