In the present study, we investigated the effect of nitric oxide (NO)
on capping, which is associated with the actin polymerization in HL-60
cells (human promyelocytic leukemia cells). We first assessed the eff
ect of NO on the patching and capping by using anti-human LFA-1 monocl
onal antibody. Samples were analyzed by a fluorescence microscope. As
expected, NO inhibited the percentage of capping dose dependently. We
compared the effect of NO on capping with cytochalasin D (CD) and obse
rved that CD also inhibits the capping in HL-60 cells. We next examine
d the effect of NO on the F-actin content. For assays of F-actin conte
nt, the FITC labelled phalloidin was permeabilized and stained in HL-6
0 cells. The bound fluorescence quantified by flow cytometry using a F
ACStar. There was a decrease in the F-actin formation in NO treated ce
lls. Taken together, these data indicate that NO inhibits the capping
on cellular membrane by decreasing the intracellular F-actin formation
in HL-60 cells. We suggest that the formation of capping linked with
actin polymerization at the inner leaflet of plasma membrane may be re
gulated by NO. (C) 1997 Academic Press.