Adhesion of neutrophils, lymphocytes and promyelocytic HL60 cells was
compared in a flow-based model in which a monolayer of activated plate
lets formed the adhesive substrate. Each type of leucocyte formed P-se
lectin-mediated rolling attachments on the platelet surface under phys
iologically relevant flow conditions. Lymphocytes adhered less, and HL
60 in similar numbers, compared to neutrophils, whereas the lymphocyte
s and HL60 cells rolled much more rapidly. Sulphated, sialylated sacch
aride(s) were implicated as ligand(s) for P-selectin for all leucocyte
s, but L-selectin (borne by neutrophils and lymphocytes, but not HL60
cells) appears to be a major presenter of ligand for neutrophils alone
. T cells enriched from peripheral blood lymphocytes adhered in greate
r numbers than B cells. Differentiation of HL60 cells to neutrophil-li
ke cells (induced by DMSO) caused cell volume to decrease and surface
expression of integrin adhesion molecules to increase, but only a smal
l percentage of cells were converted to an L-selectin-bearing phenotyp
e. Differentiated cells showed evidence of stabilization of adhesion w
ith increasing stress and a marked reduction in rolling velocity. Thes
e studies indicate that cell differentiation may be accompanied by alt
eration of adhesive behaviour, resulting from changes in physical char
acteristics as well as surface properties. Moreover, results suggest t
hat P-selectin could promote lymphocyte attachment to endothelium in a
cute inflammatory conditions and possibly mediate lymphocyte-platelet
interaction during thrombosis.