Insight into the role of low molecular weight phosphotyrosine phosphatase (LMW-PTP) on platelet-derived growth factor receptor (PDGF-r) signaling. LMW-PTP controls PDGF-r kinase activity through TYR-857 dephosphorylation

J Biol Chem. 2002 Oct 4;277(40):37331-8. doi: 10.1074/jbc.M205203200. Epub 2002 Jul 30.

Abstract

Low molecular weight phosphotyrosine phosphatase (LMW-PTP) is an enzyme involved in platelet-derived growth factor-induced mitogenesis and cytoskeleton rearrangement. Our previous results demonstrated that LMW-PTP is able to bind and dephosphorylate activated platelet-derived growth factor receptor (PDGF-r), thus inhibiting cell proliferation. Here we revisit the role of LMW-PTP on activated PDGF-r dephosphorylation. We demonstrate that LMW-PTP preferentially acts on cell surface PDGF-r, excluding the internalized activated receptor pool. Many phosphotyrosine phosphatases act by site-selective dephosphorylation on several sites of PDGF-r, but until now, there has been no evidence of a direct involvement of a specific phosphotyrosine phosphatase in the dephosphorylation of the 857 kinase domain activation tyrosine. Here we report that LMW-PTP affects the kinase activity of the receptor through the binding and dephosphorylation of Tyr-857 and influences many of the signal outputs from the receptor. In particular, we demonstrate a down-regulation of phosphatidylinositol 3-kinase, Src homology phosphatase-2, and phospholipase C-gamma1 binding but not of MAPK activation. In addition, we report a slight action of LMW-PTP on Tyr-716, which directs MAPK activation through Grb2 binding. On the basis of these results, we propose a key role for LMW-PTP in PDGF-r down-regulation through the dephosphorylation of the activation loop Tyr-857, thus determining a general negative regulation of all downstream signals, with the exception of those elicited by internalized receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Becaplermin
  • Biological Transport
  • Cell Division / physiology
  • Humans
  • Isoenzymes / physiology*
  • Kinetics
  • Mice
  • Phosphorylation
  • Phosphotyrosine / metabolism
  • Platelet-Derived Growth Factor / pharmacology
  • Protein Phosphatase 2
  • Protein Tyrosine Phosphatases / physiology*
  • Proto-Oncogene Proteins c-sis
  • Proto-Oncogene Proteins*
  • Receptors, Platelet-Derived Growth Factor / metabolism*
  • Receptors, Platelet-Derived Growth Factor / physiology*
  • Recombinant Proteins / pharmacology
  • Time Factors
  • Trypsin
  • Tumor Cells, Cultured

Substances

  • Isoenzymes
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-sis
  • Recombinant Proteins
  • Becaplermin
  • Phosphotyrosine
  • PDGF receptor tyrosine kinase
  • Receptors, Platelet-Derived Growth Factor
  • Protein Phosphatase 2
  • ACP1 protein, human
  • Acp1 protein, mouse
  • Protein Tyrosine Phosphatases
  • Trypsin