SHPS-1 negatively regulates integrin alphaIIbbeta3 function through CD47 without disturbing FAK phosphorylation

J Thromb Haemost. 2005 Apr;3(4):763-74. doi: 10.1111/j.1538-7836.2005.01235.x.

Abstract

CD47 (integrin-associated protein) serves as a receptor for thrombospondin-1 (TSP-1) and Src homology 2 domain-containing protein tyrosine phosphatase substrate-1 (SHPS-1), and the TSP-1/CD47 interaction has been believed to augment integrin-mediated platelet function. Here, employing SHPS-1-immunoglobulin (Ig) as a ligand, we have newly demonstrated that CD47 acts as an inhibitory receptor for platelet function. The binding of SHPS-1-Ig was solely mediated by CD47, because CD47-deficient platelets failed to bind murine SHPS-1-Ig. The human SHPS-1/CD47 interaction inhibited the platelet aggregation induced by several kinds of agonists at a low concentration. Moreover, human SHPS-1 expressed on the cell surface as well as soluble SHPS-1-Ig markedly inhibited the platelet spreading on, but not initial adhesion to, immobilized fibrinogen. Again, neither murine SHPS-1 expressed on the cell surface nor murine SHPS-1-Ig inhibited the spreading of CD47-deficient platelets. We further investigated the tyrosine phosphorylation of signaling proteins during platelet spreading on immobilized fibrinogen. Unexpectedly, SHPS-1 inhibited alpha(IIb)beta(3)-mediated platelet spreading without disturbing focal adhesion kinase (FAK) tyrosine phosphorylation. Further examination revealed that SHPS-1 inhibited the tyrosine phosphorylation of alpha-actinin, a downstream effector of FAK, but not of cortactin. Thus, it is likely that the SHPS-1/CD47 interaction inhibits alpha(IIb)beta(3)-mediated outside-in signaling by interfering with the downstream pathway of FAK. Taken together, our data suggest that SHPS-1 negatively regulates platelet function via CD47, especially alpha(IIb)beta(3)-mediated outside-in signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinin / metabolism
  • Animals
  • Antigens, CD / biosynthesis*
  • Antigens, Differentiation / metabolism
  • Antigens, Differentiation / physiology*
  • Blood Platelets / metabolism
  • CD47 Antigen
  • CHO Cells
  • Cell Line
  • Cell Membrane / metabolism
  • Cortactin
  • Cricetinae
  • Dose-Response Relationship, Drug
  • Fibrinogen / chemistry
  • Fibrinogen / metabolism
  • Flow Cytometry
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Gene Expression Regulation*
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / physiology*
  • Mice
  • Microfilament Proteins / metabolism
  • Phosphorylation
  • Platelet Aggregation
  • Platelet Glycoprotein GPIIb-IIIa Complex / metabolism*
  • Protein Binding
  • Protein-Tyrosine Kinases / metabolism*
  • Receptors, Immunologic / metabolism
  • Receptors, Immunologic / physiology*
  • Signal Transduction
  • Tyrosine / chemistry

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • CD47 Antigen
  • CD47 protein, human
  • CTTN protein, human
  • Cd47 protein, mouse
  • Cortactin
  • Cttn protein, mouse
  • Membrane Glycoproteins
  • Microfilament Proteins
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Ptpns1 protein, mouse
  • Receptors, Immunologic
  • SIRPA protein, human
  • Actinin
  • Tyrosine
  • Fibrinogen
  • Protein-Tyrosine Kinases
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • PTK2 protein, human
  • Ptk2 protein, mouse