Syndecan-1 transmembrane and extracellular domains have unique and distinct roles in cell spreading

J Biol Chem. 2003 Nov 21;278(47):46607-15. doi: 10.1074/jbc.M304775200. Epub 2003 Sep 14.

Abstract

Raji cells expressing syndecan-1 (Raji-S1) adhere and spread when plated on heparan sulfate-binding extracellular matrix ligands or monoclonal antibody 281.2, an antibody directed against the syndecan-1 extracellular domain. Cells plated on monoclonal antibody 281.2 initially extend a broad lamellipodium, a response accompanied by membrane ruffling at the cell margin. Membrane ruffling then becomes polarized, leading to an elongated cell morphology. Previous work demonstrated that the syndecan-1 cytoplasmic domain is not required for these activities, suggesting important roles for the syndecan-1 transmembrane and/or extracellular domains in the assembly of a signaling complex necessary for spreading. Work described here demonstrates that truncation of the syndecan-1 extracellular domain does not affect the initial lamellipodial extension in the Raji-S1 cells but does inhibit the active membrane ruffling that is necessary for cell polarization. Replacement of the entire syndecan-1 transmembrane domain with leucine residues completely blocks the cell spreading. These data demonstrate that the syndecan-1 transmembrane and extracellular domains have important but distinct roles in Raji-S1 cell spreading; the extracellular domain mediates an interaction that is necessary for dynamic cytoskeletal rearrangements whereas an interaction of the transmembrane domain is required for the initial spreading response.

Publication types

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

MeSH terms

  • Cell Adhesion*
  • Cell Line, Tumor
  • Cell Membrane / ultrastructure
  • Cell Polarity
  • Cell Size
  • Cytoskeleton
  • Humans
  • Membrane Glycoproteins / chemistry*
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / physiology*
  • Membrane Microdomains / metabolism
  • Microscopy, Video
  • Mutagenesis, Site-Directed
  • Protein Structure, Tertiary
  • Proteoglycans / chemistry*
  • Proteoglycans / metabolism
  • Proteoglycans / physiology*
  • Sequence Deletion
  • Syndecan-1
  • Syndecans

Substances

  • Membrane Glycoproteins
  • Proteoglycans
  • SDC1 protein, human
  • Syndecan-1
  • Syndecans