The recognition of extracellular molecules by cell surface receptors i
s the principal mechanism used by cells to sense their environment. Co
nsequently, signals transduced as a result of these interactions make
a major contribution to the regulation of cellular phenotype. Historic
ally, particular emphasis has been placed on elucidating the intracell
ular consequences of growth factor and cytokine binding to cells. In a
ddition to these interactions, however, cells are usually in intimate
contact with a further source of complex structural and functional inf
ormation, namely immobilised extracellular matrix and/or cell surface
adhesion proteins. A key question in recent years has been whether cel
ls use the myriad of adhesion protein-receptor interactions purely for
structural and migratory function, or whether these interactions also
make a more varied contribution to cell phenotype. Here we review dyn
amic aspects of the function of one major class of adhesion receptor,
the integrins. In particular, we focus on the evidence for shape chang
es in integrin molecules, the mechanisms responsible for regulating li
gand binding, and the signals transduced following integrin occupancy.