The aim of this work was to examine the possible influence of the integrity
of the microtubule network on the plasma membrane fluidity of L929 mouse f
ibroblasts. The L929 cell line was selected for the ease of culture and the
stability of its characteristics. The cells were treated with colchicine,
nocodazole and vinblastine, three microtubule-depolymerizing drugs, at vari
ous concentrations and for various times. Membrane fluidity was assessed fr
om fluorescence depolarization measurements with the plasma membrane probe
TMA-DPH. Each of the drugs induced a significant, dose-dependent decrease i
n fluorescence anisotropy. The effect levelled off (5-7% decrease) after si
milar to 90 min of treatment, and could be unambiguous ly interpreted as re
sulting from an increase in membrane fluidity. The cumulative action of the
drugs did not significantly increase the effect. The effects of colchicine
and nocodazole could be reversed by incubation in drug-free medium, but no
t that of vinblastine. The results are discussed in correlation with the ki
netics of the three drugs interaction with tubulin or microtubules. It is c
oncluded that the microtubule integrity contributed to the high plasma memb
rane lipidic order, but less than other factors, like the lipid composition
and the cholesterol content.