The Lutheran/Basal Cell Adhesion Molecule Promotes Tumor Cell Migration by Modulating Integrin-mediated Cell Attachment to Laminin-511 Protein
The Lutheran/Basal Cell Adhesion Molecule Promotes Tumor Cell Migration by Modulating Integrin-mediated Cell Attachment to Laminin-511 Protein
Cell-matrix interactions are critical for tumor cell migration. Lutheran (Lu), also known as basal cell adhesion molecule (B-CAM), competes with integrins for binding to laminin α5, a subunit of LM-511, a major component of basement membranes. Here we show that the preferential binding of Lu/B-CAM to laminin α5 promotes tumor cell migration. The attachment of Lu/B-CAM transfectants to LM-511 was slightly weaker than that of control cells, and this was because Lu/B-CAM disturbed integrin binding to laminin α5. Lu/B-CAM induced a spindle cell shape with pseudopods and promoted cell migration on LM-511. In addition, blocking with an anti-Lu/B-CAM antibody led to a flat cell shape and inhibited migration on LM-511, similar to the effects of an activating integrin β1 antibody. We conclude that tumor cell migration on LM-511 requires that Lu/B-CAM competitively modulates cell attachment through integrins. We suggest that this competitive interaction is involved in a balance between static and migratory cell behaviors.
- University of Mary United States
- Keio University Japan
- Tokyo University of Pharmacy and Life Sciences Japan
- Washington University in St. Louis United States
Mice, Knockout, Integrins, Membrane Glycoproteins, Lutheran Blood-Group System, Basement Membrane, Neoplasm Proteins, Mice, HEK293 Cells, Cell Movement, Cell Line, Tumor, Neoplasms, Cell Adhesion, Animals, Humans, Laminin, Cell Adhesion Molecules, Cell Shape
Mice, Knockout, Integrins, Membrane Glycoproteins, Lutheran Blood-Group System, Basement Membrane, Neoplasm Proteins, Mice, HEK293 Cells, Cell Movement, Cell Line, Tumor, Neoplasms, Cell Adhesion, Animals, Humans, Laminin, Cell Adhesion Molecules, Cell Shape
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