Deleted in colorectal carcinoma (DCC) binds heparin via its fifth fibronectin type III domain

J Biol Chem. 1997 Oct 24;272(43):26940-6. doi: 10.1074/jbc.272.43.26940.

Abstract

DCC (deleted in colorectal carcinoma) is a broadly expressed cell-surface receptor. Netrin-1 was recently identified as a DCC ligand in brain, but the possibility of other DCC ligands was suggested by the finding that an anti-DCC antibody (clone AF5) neutralized netrin-1-dependent commissural axon outgrowth without blocking DCC/netrin-1 interactions. Here we have searched for alternative cell-surface DCC ligands. A DCC-Ig fusion protein bound to neural and epithelial derived cell lines, indicating that these lines express ligand(s) for DCC. The cell-surface binding activity was mediated by the loop between beta-strands F and G of the fifth fibronectin type III repeat FNIII-D5. The loop included the sequence KNRR, which resembles heparin-binding motifs in other proteins. Heparinase and heparitinase treatment of cells reduced binding of DCC-Ig, suggesting that heparan sulfate proteoglycans are cell-surface DCC ligand(s). This was further supported by heparin blocking experiments and by binding of DCC-Ig to immobilized heparan sulfate. The interaction between DCC-Ig and heparan sulfate/heparin, both on the surface of cells and immobilized on plastic, was blocked by the same anti-DCC antibody that blocks netrin-1-dependent commissural axon outgrowth. Taken together, these findings suggest that the DCC-Ig/heparin interaction may contribute to the biological activity of DCC.

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Cell Adhesion Molecules / chemistry*
  • Cell Adhesion Molecules / metabolism*
  • Cell Line
  • Cell Membrane / metabolism
  • Colorectal Neoplasms
  • DCC Receptor
  • Fibronectins / chemistry*
  • Genes, Tumor Suppressor
  • Heparin / chemistry
  • Heparin / metabolism*
  • Humans
  • Molecular Sequence Data
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Polymerase Chain Reaction
  • Protein Structure, Secondary*
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Tumor Suppressor Proteins*

Substances

  • Cell Adhesion Molecules
  • DCC Receptor
  • DCC protein, human
  • Fibronectins
  • Peptide Fragments
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins
  • Tumor Suppressor Proteins
  • Heparin