Surface densities of ephrin-B1 determine EphB1-coupled activation of cell attachment through alpha vbeta 3 and alpha 5beta 1 integrins

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Abstract
Receptors of the Eph family and their ligands (ephrins) mediate developmental vascular assembly and direct axonal guidance. Migrating cell processes identify appropriate targets within migratory fields based on topographically displayed ephrin gradients. Here, EphB1 regulated cell attachment by discriminating the density at which ephrin‐B1 was displayed on a reconstituted surface. EphB1–ephrin‐B1 engagement did not promote cell attachment through mechanical tethering, but did activate integrin‐mediated attachment. In endothelial cells, attachment to RGD peptides or fibrinogen was mediated through αvβ3 integrin. EphB1 transfection conferred ephrin‐B1‐responsive activation of α5β1 integrin‐mediated cell attachment in human embryonic kidney cells. Activation‐competent but signaling‐defective EphB1 point mutants failed to stimulate ephrin‐B1 dependent attachment. These findings lead us to propose that EphB1 functions as a ‘ligand density sensor’ to signal integrin‐mediated cell–matrix attachment.