Thrombospondin stimulates focal adhesion disassembly through Gi- and phosphoinositide 3-kinase-dependent ERK activation

J Biol Chem. 2002 Jun 7;277(23):20453-60. doi: 10.1074/jbc.M112091200. Epub 2002 Mar 28.

Abstract

The matricellular protein thrombospondin (TSP) stimulates stress fiber and focal adhesion disassembly through a sequence (hep I) in its heparin-binding domain. TSP/hep I signals focal adhesion disassembly by binding cell surface calreticulin (CRT) and activating phosphoinositide 3-kinase (PI3K). However, other components of this signaling pathway have not been identified. We now show that TSP induces focal adhesion disassembly through activation of pertussis toxin (PTX)-sensitive G proteins and ERK phosphorylation. PTX pretreatment inhibits TSP/hep I-mediated focal adhesion disassembly as well as PI3K activation. In addition, membrane-permeable Galpha(i2)- and Gbetagamma-blocking peptides inhibit hep I-mediated focal adhesion disassembly. Hep I stimulates a transient increase in ERK activation, which is abrogated by both PTX and PI3K inhibitors. Inhibiting ERK activation with MEK inhibitors blocks hep I-mediated focal adhesion disassembly, indicating that ERK activation is required for cytoskeletal reorganization. G protein signals and ERK phosphorylation are induced by TSP binding to cell surface CRT, because CRT null mouse embryonic fibroblasts (MEF) fail to stimulate ERK phosphorylation in response to TSP/hep I treatment. These data show that G(i) protein and ERK, in concert with PI3K, are stimulated by TSP.CRT interactions at the cell surface to induce de-adhesive changes in the cytoskeleton.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cattle
  • Cell Adhesion / physiology*
  • Cell Line
  • Enzyme Activation
  • Heterotrimeric GTP-Binding Proteins / metabolism
  • Humans
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism*
  • Molecular Sequence Data
  • Pertussis Toxin
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation
  • Thrombospondins / physiology*
  • Virulence Factors, Bordetella / pharmacology

Substances

  • Thrombospondins
  • Virulence Factors, Bordetella
  • Pertussis Toxin
  • Phosphatidylinositol 3-Kinases
  • Mitogen-Activated Protein Kinases
  • Heterotrimeric GTP-Binding Proteins