In numerous investigations it has been found that natural killer (NK)
cells are among the cells arriving early at the site of defense. To re
ach the tissue sites of defense, the circulating NK cells have to pene
trate through the capillary wall and actively migrate along the matrix
proteins towards the tumor or infected target cells. For this process
NK cells need adhesion receptors which do not anchor them but allow r
eversible binding. The migration capacity of NK cells is found to be h
igher than that of other lymphocytes. NK cells also have the ability t
o increase rapidly the migratory response. IL-2 and a peptide derived
from ICAM-2 are potential inducers of NK cell migration. ICAM-2 is exp
ressed on endothelium, a site where lymphocytes start migration. Also,
a matrix protein, fibronectin, increases NK cell migration. This revi
ew focuses on the migratory capacity of NK cells and on the receptors
which NK cells use when they migrate on different substrata.