The anti-adhesive activity of thrombospondin is mediated by the N-terminal domain of cell surface calreticulin

J Biol Chem. 2002 Oct 4;277(40):37219-28. doi: 10.1074/jbc.M202200200. Epub 2002 Jul 29.

Abstract

Thrombospondin (TSP) induces reorganization of the actin cytoskeleton and restructuring of focal adhesions through binding of amino acids (aa) 17-35 (hep I peptide) of thrombospondin to a cell surface form of calreticulin (CRT). In this report we provide further evidence for the involvement of calreticulin in thrombospondin signaling and characterize thrombospondin-calreticulin interactions. Wild type but not crt(-/-) cells respond to hep I/TSP. Responsiveness can be restored by incubation of cells with exogenous calreticulin or by transfection with calreticulin. Thrombospondin forms complexes with the CRT-N-domain that are enhanced by physiologic levels of calcium and zinc. Consistent with thrombospondin/CRT-N-domain binding, only the CRT-N-domain blocks hep I- and thrombospondin-stimulated focal adhesion disassembly. A series of glutathione S-transferase-N-domain mutants were used to map the sequence within the N-domain that interacts with TSP/hep I. A construct containing aa 1-43 but not a construct of aa 1-31 supported thrombospondin binding and focal adhesion disassembly. A series of overlapping peptides were used to further map the thrombospondin-binding site. Peptides spanning aa 19-36 (RWIESKHKSDFGKFVLSS) blocked hep I-stimulated focal adhesion disassembly, indicating that the TSP/hep I-binding site is located to this sequence in calreticulin. A mutant fusion protein lacking aa 19-36 (glutathione S-transferase-CRTDeltahep I) failed to restore responsiveness to hep I in crt(-/-) cells, bind thrombospondin, or competitively block focal adhesion disassembly, providing evidence for the role of this calreticulin sequence in mediating thrombospondin signaling.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aorta
  • Base Sequence
  • Blood Platelets / physiology
  • Calreticulin / chemistry
  • Calreticulin / genetics
  • Calreticulin / physiology*
  • Cell Adhesion / drug effects
  • Cell Adhesion / physiology*
  • Cell Line
  • Cell Membrane / physiology
  • DNA Primers
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / physiology
  • Humans
  • Mice
  • Molecular Chaperones / chemistry
  • Molecular Chaperones / physiology
  • Molecular Sequence Data
  • Peptide Fragments / pharmacology
  • Polymerase Chain Reaction
  • Rabbits
  • Thrombospondin 1 / chemistry
  • Thrombospondin 1 / pharmacology
  • Thrombospondin 1 / physiology*
  • Thrombospondins / physiology*

Substances

  • Calreticulin
  • DNA Primers
  • Molecular Chaperones
  • Peptide Fragments
  • Thrombospondin 1
  • Thrombospondins