The chemokines participate in an exceptional range of physiological and pat
hological processes, including the control of lymphocyte trafficking, tumor
growth, wound healing, allograft rejection, regulation of T-cell different
iation, asthma, infection with HIV and atherosclerosis. This vast array of
activities is triggered by the interaction of nearly 50 different chemokine
s with a relatively modest number of 20 G-protein-coupled receptors. The as
ymmetry between the number of receptors and ligands suggests an underlying,
shared control mechanism activated at a very early stage of the response.
One of the first events triggered by the binding of chemokines is the homo-
and heterodimerization of their receptors; here, we outline these events a
nd their consequences in chemokine signaling.