Ephrin-A5 induces rounding, blebbing and de-adhesion of EphA3-expressing 293T and melanoma cells by CrkII and Rho-mediated signalling

J Cell Sci. 2002 Mar 1;115(Pt 5):1059-72. doi: 10.1242/jcs.115.5.1059.

Abstract

Eph receptor tyrosine kinases and ephrins regulate morphogenesis in the developing embryo where they effect adhesion and motility of interacting cells. Although scarcely expressed in adult tissues, Eph receptors and ephrins are overexpressed in a range of tumours. In malignant melanoma, increased Eph and ephrin expression levels correlate with metastatic progression. We have examined cellular and biochemical responses of EphA3-expressing melanoma cell lines and human epithelial kidney 293T cells to stimulation with polymeric ephrin-A5 in solution and with surfaces of defined ephrin-A5 densities. Within minutes, rapid reorganisation of the actin and myosin cytoskeleton occurs through activation of RhoA, leading to the retraction of cellular protrusions, membrane blebbing and detachment, but not apoptosis. These responses are inhibited by monomeric ephrin-A5, showing that receptor clustering is required for this EphA3 response. Furthermore, the adapter CrkII, which associates with tyrosine-phosphorylated EphA3 in vitro, is recruited in vivo to ephrin-A5-stimulated EphA3. Expression of an SH3-domain mutated CrkII ablates cell rounding, blebbing and detachment. Our results suggest that recruitment of CrkII and activation of Rho signalling are responsible for EphA3-mediated cell rounding, blebbing and de-adhesion, and that ephrin-A5-mediated receptor clustering and EphA3 tyrosine kinase activity are essential for this response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / drug effects
  • Actin Cytoskeleton / metabolism*
  • Cell Adhesion / drug effects
  • Cell Adhesion / physiology*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cell Size / drug effects
  • Cell Size / physiology*
  • Ephrin-A5
  • Gene Expression Regulation, Neoplastic / physiology
  • Humans
  • Melanoma / metabolism*
  • Melanoma / physiopathology
  • Membrane Proteins / metabolism*
  • Membrane Proteins / pharmacology
  • Mutation / physiology
  • Phosphotransferases / metabolism
  • Protein Kinases / metabolism*
  • Protein Structure, Tertiary / genetics
  • Proto-Oncogene Proteins c-crk
  • Proto-Oncogene Proteins*
  • Pseudopodia / drug effects
  • Pseudopodia / ultrastructure
  • Receptor Protein-Tyrosine Kinases / drug effects
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Receptor, EphA7
  • Tumor Cells, Cultured
  • Tyrosine / genetics
  • rho GTP-Binding Proteins / metabolism*

Substances

  • Ephrin-A5
  • Membrane Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-crk
  • Tyrosine
  • Phosphotransferases
  • Protein Kinases
  • Receptor Protein-Tyrosine Kinases
  • Receptor, EphA7
  • rho GTP-Binding Proteins