Lactogen-dependent Nb2 lymphoma cells, widely employed for studying pr
olactin (PRL) mitogenic mechanisms, are also useful for investigations
of apoptosis in T-lineage lymphocytes, Utilizing PRL-dependent Nb2-11
cultures, apoptosis-regulatory genes were evaluated for participation
in dexamethasone- (DE);) provoked cell death or its inhibition by PRL
, Treatment of lactogen-starved, G(1)-arrested Nb2-11 cells with DEX (
100 nM) activated apoptosis within 12 h evaluated by flow cytometric a
nalysis of fragmented DNA, This effect was not associated with altered
expression of bcl-2, bax, or pim-1. PRL (10 ng/mL), coincubated with
DEX-treated cells, completely blocked DEX-induced apoptosis. This inhi
bition was associated with increased expression of bcl-2 anal pim-1 mR
NAs, genes reported to suppress apoptosis, within 2-6 h after addition
of the hormone. Moreover, the increased transcription of bcl-2 and pi
m-1 was coupled to increases in their protein levels. The results sugg
est that bcl-2, bax, and pim-1 do not play a critical role in DEX-indu
ced apoptosis in Nb2 cells. However, expression of bcl-2, together wit
h pim-1, may have a role in mediating the antiapoptotic actions of PRL
.