Sc. Strauss et al., PKC-DEPENDENT AND PKC-INDEPENDENT CELLULAR EFFECTS INDUCED BY RECOMBINANT TRANSFORMING GROWTH-FACTOR TYPE-BETA-1, International journal of oncology, 7(3), 1995, pp. 565-572
TGF-beta 1 purified from human platelets induces colony formation of r
at fibroblasts reversibly when administered together with EGF. TGF-bet
a 1 has been reported by us to lead to stable transformation of rat fi
broblasts, to activate latent Epstein-Barr virus, to exhibit tumor pro
moting activity for murine fibroblasts, and to cause the release of ap
optosis-inducing signals from normal cells which are directed specific
ally against transformed cells. The use of recombinant TGF-beta 1 in t
his study showed that all the effects measured were indeed due to TGF-
beta 1. In order to get information on intracellular signal pathways i
nduced by TGF-beta 1, specific inhibitors of protein kinase C (PKC) we
re applied. Induction of EBV antigens by TGF-beta 1 was dependent on t
he function of PKC, whereas induction of apoptosis in transformed cell
s by TGF-beta 1-treated normal cells was independent of the action of
PKC.