Va. Edgar et al., FLUOXETINE ACTION ON MURINE T-LYMPHOCYTE PROLIFERATION - PARTICIPATION OF PKC ACTIVATION AND CALCIUM MOBILIZATION, Cellular signalling, 10(10), 1998, pp. 721-726
The present study was undertaken to analyse the effect of fluoxetine u
pon murine T-lymphocyte proliferation. We found that fluoxetine exerte
d a dual effect, which depended on the degree of lymphocyte activation
: at mitogenic concentration (2 mu g/mL) of concavalin A (Con A), we o
bserved an inhibitory effect on cellular proliferation, whereas, on su
bmitogenic Con A concentration (1 mu g/mL), fluoxetine stimulated the
cellular response. Given these facts, we studied PKC activation and ca
lcium mobilisation in both stimulatory and inhibitory effects of fluox
etine on T-cell proliferation. We observed that fluoxetine increased P
KC translocation obtained with 1 mu g/mL Con A concentration, whereas
PKC was degraded when 2 mu g/mL was used. This mechanism is thought to
be mediated by calcium mobilisation. According to our results, fluoxe
tine seemed to modulate calcium influx, which, in turn, would influenc
e PKC translocation, modulating the immune response. CELL SIGNAL. 10;1
0:721-726, 1998. (C) Elsevier Science Inc.