A peptide corresponding to the C-terminal region of pleiotrophin inhibits angiogenesis in vivo and in vitro

J Cell Biochem. 2011 Jun;112(6):1532-43. doi: 10.1002/jcb.23066.


Pleiotrophin (PTN) is a heparin-binding growth factor that plays a significant role in tumor growth and angiogenesis. We have previously shown that in order for PTN to induce migration of endothelial cells, binding to both α(ν) β(3) integrin and its receptor protein tyrosine phosphatase beta/zeta (RPTPβ/ζ) is required. In the present study we show that a synthetic peptide corresponding to the last 25 amino acids of the C-terminal region of PTN (PTN(112-136) ) inhibited angiogenesis in the in vivo chicken embryo chorioallantoic membrane (CAM) assay and PTN-induced migration and tube formation of human endothelial cells in vitro. PTN(112-136) inhibited binding of PTN to α(ν) β(3) integrin, and as shown by surface plasmon resonance (SPR) measurements, specifically interacted with the specificity loop of the extracellular domain of β(3) . Moreover, it abolished PTN-induced FAK Y397 phosphorylation, similarly to the effect of a neutralizing α(ν) β(3) -selective antibody. PTN(112-136) did not affect binding of PTN to RPTPβ/ζ in endothelial cells and induced β(3) Y773 phosphorylation and ERK1/2 activation to a similar extent with PTN. This effect was inhibited by down-regulation of RPTPβ/ζ by siRNA or by c-src inhibition, suggesting that PTN(112-136) may interact with RPTPβ/ζ. NMR spectroscopy studies showed that PTN(112-136) was characterized by conformational flexibility and absence of any element of secondary structure at room temperature, although the biologically active peptide segment 123-132 may adopt a defined structure at lower temperature. Collectively, our data suggest that although PTN(112-136) induces some of the signaling pathways triggered by PTN, it inhibits PTN-induced angiogenic activities through inhibition of PTN binding to α(ν) β(3) integrin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Carrier Proteins / chemistry*
  • Carrier Proteins / metabolism
  • Cell Movement / drug effects
  • Cells, Cultured
  • Chick Embryo
  • Cytokines / chemistry*
  • Cytokines / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Immunoprecipitation
  • Integrin alphaVbeta3 / metabolism
  • Magnetic Resonance Spectroscopy
  • Neovascularization, Physiologic / drug effects*
  • Peptides / chemical synthesis
  • Peptides / chemistry
  • Peptides / pharmacology*
  • Phosphorylation / drug effects
  • Protein Binding / drug effects
  • RNA Interference
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5 / metabolism


  • Carrier Proteins
  • Cytokines
  • Integrin alphaVbeta3
  • Peptides
  • pleiotrophin
  • Receptor-Like Protein Tyrosine Phosphatases, Class 5