Basal cell adhesion molecule/lutheran protein. The receptor critical for sickle cell adhesion to laminin

J Clin Invest. 1998 Jun 1;101(11):2550-8. doi: 10.1172/JCI1204.

Abstract

Sickle red cells bind significant amounts of soluble laminin, whereas normal red cells do not. Solid phase assays demonstrate that B-CAM/LU binds laminin on intact sickle red cells and that red cell B-CAM/LU binds immobilized laminin, whereas another putative laminin binding protein, CD44, does not. Ligand blots also identify B-CAM/LU as the only erythrocyte membrane protein(s) that binds laminin. Finally, transfection of murine erythroleukemia cells with human B-CAM cDNA induces binding of both soluble and immobilized laminin. Thus, B-CAM/LU appears to be the major laminin-binding protein of sickle red cells. Previously reported overexpression of B-CAM/LU by epithelial cancer cells suggests that this protein may also serve as a laminin receptor in malignant tumors.

Publication types

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

MeSH terms

  • Anemia, Sickle Cell / blood*
  • Animals
  • Blotting, Western
  • Cell Adhesion Molecules / metabolism*
  • Erythrocytes / metabolism*
  • Humans
  • Laminin / metabolism*
  • Lutheran Blood-Group System
  • Mice
  • Neoplasm Proteins / metabolism*
  • Receptors, Laminin / metabolism*
  • Recombinant Proteins / metabolism

Substances

  • BCAM protein, human
  • Cell Adhesion Molecules
  • Laminin
  • Lutheran Blood-Group System
  • Neoplasm Proteins
  • Receptors, Laminin
  • Recombinant Proteins