The 140-kilodalton antiangiogenic fragment of thrombospondin-1 binds to basic fibroblast growth factor

Cell Growth Differ. 1997 Apr;8(4):471-9.

Abstract

Thrombospondin-1 (TSP) inhibits the angiogenic activity of basic fibroblast growth factor (bFGF). Here we address the hypothesis of a direct interaction between TSP and bFGF. Gel permeation chromatography and cross-linking experiments demonstrated that bFGF binds to TSP in solution. bFGF also bound to immobilized TSP in a solid-phase assay. Binding was dose-dependent, with a Kd in the nanomolar range, and was inhibited by anti-TSP antibodies. The 140-kDa carboxyl-terminal fragment of TSP, but not the 25-kDa heparin-binding fragment, fully retained the bFGF binding capacity. Accordingly, binding was inhibited by monoclonal antibodies directed against this fragment. Heparin completely blocked bFGF binding to TSP and to the 140-kDa fragment. TSP and its 140-kDa fragment inhibited the binding of bFGF to endothelial cells at concentrations (> or = 100 nM) that inhibited endothelial cell proliferation but not motility. Low-affinity binding was inhibited more than high-affinity binding (up to 76 and 41% inhibition, respectively), and the inhibition was reversed by anti-TSP antibodies. Vitronectin and transforming growth factor beta, potentially associated with TSP, did not affect bFGF binding to endothelial cells. Although TSP did not affect the activation of the high-affinity receptors, it reduced the long-term internalization of bFGF. We conclude that TSP binds to bFGF through a domain within its 140-kDa fragment, a mechanism that might affect bFGF interaction with endothelial cells, activity, and association with the extracellular matrix.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Cell Adhesion Molecules / metabolism*
  • Cell Division
  • Cell Movement
  • Endothelium, Vascular / cytology
  • Fibroblast Growth Factor 2 / metabolism*
  • Heparin / metabolism
  • Membrane Glycoproteins / metabolism*
  • Molecular Weight
  • Neovascularization, Physiologic*
  • Peptide Fragments / metabolism
  • Protein Binding
  • Thrombospondins

Substances

  • Cell Adhesion Molecules
  • Membrane Glycoproteins
  • Peptide Fragments
  • Thrombospondins
  • Fibroblast Growth Factor 2
  • Heparin