Binding of heparin and compound Y to endothelial cells stimulates the synthesis of an antithrombotic heparan sulfate proteoglycan

Braz J Med Biol Res. 1994 Sep;27(9):2191-5.

Abstract

The mechanism by which heparin and antithrombotic agents, including a cyclic octaphenolsulfonic acid (compound Y), stimulate the synthesis of an antithrombotic heparan sulfate by endothelial cells in culture was investigated. Compound Y increases the amount of heparan sulfate from the cell surface and secreted to the medium by endothelial cells by three-fold. Binding experiments have shown saturation of the endothelial cell receptors at a concentration of 0.16 microM for heparin and 2.7 microM for compound Y. The kinetic binding constants (Ks) for compound Y and heparin were 1,333 nM and 42 nM, respectively. It was also shown that both compounds bind to the same receptors. The Scatchard plots indicated that 1,319 nmoles compound Y and 35 nmoles heparin bound per microgram cell protein, indicating that 40-fold more molecules of compound Y bound to the receptors when compared to heparin. No significant internalization of the compounds was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Guinea Pigs
  • Heparan Sulfate Proteoglycans
  • Heparin / metabolism*
  • Heparitin Sulfate / biosynthesis*
  • Protein Binding
  • Proteoglycans / biosynthesis*
  • Rabbits
  • Sulfonic Acids / metabolism*
  • Time Factors

Substances

  • Heparan Sulfate Proteoglycans
  • Proteoglycans
  • Sulfonic Acids
  • Heparin
  • Heparitin Sulfate