K. Kawabata et al., THE CHANGES OF MAC-1 AND L-SELECTIN EXPRESSION ON GRANULOCYTES AND SOLUBLE L-SELECTIN LEVEL DURING HEMODIALYSIS, Nephron, 73(4), 1996, pp. 573-579
L-selectin and Mac-1 expressed on leukocytes are critical for leukocyt
e adhesion to inflamed endothelium. L-selectin is known to be rapidly
shed from the cell surface of granulocytes after activation. In the pr
esent study the change of expressions of these adhesion molecules on g
ranulocytes were analyzed by flow cytometry, and the serum concentrati
on of shed L-selectin (soluble Lr selectin; sL-selectin) was measured
by enzyme-linked immunosorbent assay (ELISA) during hemodialysis in pa
tients treated with regenerated cellulose membranes (RC group) versus
polysulfone membranes (PS group). In the RC group, Mac-1 expression on
granulocytes increased significantly at 30 min after the initiation o
f hemodialysis (p < 0.05) compared with predialysis values, coinciding
with the nadir of dialysis-induced granulocytopenia. Granulocyte L-se
lectin expression decreased significantly at 15 min after the initiati
on of hemodialysis (p < 0.05) and remained decreased through the cours
e of dialysis session, compared with predialysis values. Serum sL-sele
ctin level significantly increased at 15 min after the initiation of h
emodialysis (p < 0.05), compared with predialysis values. In the PS gr
oup, no significant variation in Mac-1 and L-selectin expression on gr
anulocytes and serum sL-selectin level were detected. This reciprocal
change of Mac-1 and L-selectin on granulocyte cell surface was attribu
ted to development of granulocytopenia and subsequent reversal during
dialysis with cellulose membranes. In this study, we confirmed the she
dding of L-selectin during cellulosic dialysis by ELISA. The increase
in sL-selectin, which has potential activity of inhibiting L-selectin-
dependent adhesion of granulocyte to endothelium, might be involved in
rebound granulocytosis during dialysis with cellulose membranes and i
mpairment of the granulocyte function in patients on chronic hemodialy
sis.