Stabilin-2 mediates homophilic cell-cell interactions via its FAS1 domains

FEBS Lett. 2009 Apr 17;583(8):1375-80. doi: 10.1016/j.febslet.2009.03.046. Epub 2009 Mar 26.

Abstract

Stabilin-2 was recently shown to mediate a heterophilic interaction with integrin alpha M beta 2 via its FAS1 domain. Here, we demonstrate that stabilin-2 also mediates homophilic cell-cell interactions. L cells expressing stabilin-2 mediate a significant level of cell aggregation, and this aggregation is significantly inhibited by anti-stabilin-2 antibody. Stabilin-2-mediated aggregation is mediated by homophilic interactions and enhanced in the presence of Ca(2+) and Mg(2+). Interestingly, exogenous addition of FAS1 domains but not EGF-like domains enhances stabilin-2-mediated cell aggregation, suggesting that exogenous FAS1 domains may form polymeric structure with FAS1 domains of stabilin-2. Together, these data show the participation of stabilin-2 in homophilic cell adhesion and role of FAS1 domains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / chemistry
  • Cell Adhesion Molecules, Neuronal / physiology*
  • Cell Adhesion*
  • Cell Line
  • Mice
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism

Substances

  • Cell Adhesion Molecules, Neuronal
  • Recombinant Proteins
  • Stab2 protein, mouse