TAG-1/axonin-1 is a high-affinity ligand of neurocan, phosphacan/protein-tyrosine phosphatase-zeta/beta, and N-CAM

J Biol Chem. 1996 Jun 28;271(26):15716-23. doi: 10.1074/jbc.271.26.15716.

Abstract

Proteoglycans appear to play an important role in modulating cell-cell and cell-matrix interactions during nervous tissue histogenesis. The nervous tissue-specific chondroitin sulfate proteoglycans neurocan and phosphacan/protein-tyrosine phosphatase-zeta/beta were found to be high-affinity ligands of the neural cell adhesion molecule TAG-1/axonin-1, with dissociation constants of 0.3 nM and 0.04 nM, respectively. Phosphacan binding was decreased by approximately 70% following chondroitinase treatment, whereas binding of neurocan was not affected. The contribution of chondroitin sulfate chains to the binding of neurocan and phosphacan to TAG-1/axonin-1 is therefore the opposite of that previously observed for their binding to two other Ig-superfamily neural cell adhesion molecules, Ng-CAM/L1 and N-CAM. Moreover, whereas phosphacan interactions with certain proteins are mediated at least in part by N-linked oligosaccharides on the proteoglycan, N-deglycosylation of phosphacan had no effect on its binding to TAG-1/axonin-1. In addition to the chondroitin sulfate proteoglycans described above, we have demonstrated that N-CAM is a high-affinity ligand of TAG-1/axonin-1 (Kd approximately 1 nM), and specific binding of TAG-1/axonin-1 to tenascin-C was also observed (Kd approximately 9 nM). Immunocytochemical studies of embryonic and early postnatal nervous tissue showed an overlapping localization of TAG-1/axonin-1 with all four of these ligands, further supporting the biological significance of their ability to interact in vitro.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Chondroitin Sulfate Proteoglycans / metabolism*
  • Contactin 2
  • Extracellular Matrix Proteins / metabolism
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Lectins, C-Type
  • Ligands
  • Nerve Tissue Proteins / metabolism*
  • Nervous System / embryology
  • Nervous System / metabolism
  • Neurocan
  • Phosphoprotein Phosphatases / metabolism*
  • Protein Binding
  • Proteoglycans / metabolism
  • Rats
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5
  • Receptors, Growth Factor / metabolism
  • Tenascin / metabolism

Substances

  • CNTN2 protein, human
  • Cell Adhesion Molecules, Neuronal
  • Chondroitin Sulfate Proteoglycans
  • Cntn2 protein, rat
  • Contactin 2
  • Extracellular Matrix Proteins
  • Lectins, C-Type
  • Ligands
  • Nerve Tissue Proteins
  • Neurocan
  • Proteoglycans
  • Receptors, Growth Factor
  • Tenascin
  • NCAN protein, human
  • Phosphoprotein Phosphatases
  • PTPRZ1 protein, human
  • Ptprz1 protein, rat
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5