Administration of recombinant P-selectin glycoprotein ligand Fc fusion protein suppresses inflammation and neointimal formation in Zucker diabetic rat model

Arterioscler Thromb Vasc Biol. 2002 Oct 1;22(10):1598-603. doi: 10.1161/01.atv.0000032676.20514.8f.

Abstract

Objective: P-selectin-mediated leukocyte-endothelium and leukocyte-platelet interaction has been reported after vascular injury and has been correlated with neointimal hyperplasia, but its role in neointimal formation after arterial injury in diabetes has not been described.

Methods and results: Using a Zucker diabetic rat balloon injury model, we examined the role of P-selectin in the vascular inflammatory process and neointimal formation after balloon injury. Immunohistochemistry revealed that P-selectin was intensely expressed and that CD45-positive leukocyte infiltration was significantly increased after arterial injury. A single preprocedural intravenous administration of a recombinant P-selectin-soluble glycoprotein ligand-Ig inhibited CD45-positive leukocyte accumulation and suppressed neointimal formation in the Zucker diabetic rat model.

Conclusions: These results suggest that reduction of P-selectin-mediated leukocyte activation with the use of recombinant P-selectin-soluble glycoprotein ligand-Ig decreases the inflammatory response and limits neointimal formation after balloon injury in diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Carotid Artery Injuries / complications
  • Carotid Artery Injuries / etiology
  • Carotid Stenosis / etiology
  • Carotid Stenosis / prevention & control
  • Catheterization / adverse effects
  • Cell Line
  • Cricetinae
  • Diabetes Complications
  • Diabetes Mellitus / pathology
  • Disease Models, Animal*
  • Immunoglobulin Fc Fragments / administration & dosage
  • Immunoglobulin Fc Fragments / pharmacology*
  • Immunoglobulin Fc Fragments / therapeutic use
  • Inflammation / pathology
  • Inflammation / prevention & control
  • Injections, Intravenous
  • Leukocyte Common Antigens / metabolism
  • Leukocyte Count
  • Leukocytes / metabolism
  • Leukocytes / physiology
  • Ligands
  • Membrane Glycoproteins / administration & dosage
  • Membrane Glycoproteins / pharmacology*
  • Membrane Glycoproteins / therapeutic use
  • P-Selectin / biosynthesis
  • P-Selectin / physiology
  • Rats
  • Rats, Zucker
  • Recombinant Fusion Proteins / administration & dosage
  • Recombinant Fusion Proteins / pharmacology*
  • Recombinant Fusion Proteins / therapeutic use
  • Secondary Prevention
  • Tunica Intima / pathology*

Substances

  • Immunoglobulin Fc Fragments
  • Ligands
  • Membrane Glycoproteins
  • P-Selectin
  • P-selectin ligand protein
  • Recombinant Fusion Proteins
  • Leukocyte Common Antigens