Inhibition of Bcl-2-dependent cell survival by a caspase inhibitor: a possible new pathway for Bcl-2 to regulate cell death
Résumé
The REtsAF cell line expresses a temperaturesensitive mutant of the SV40 large tumor antigen. At restrictive temperature (39.5³C), the cells undergo p53-mediated apoptosis, which can be inhibited by Bcl-2. Here, we show that Z-VADfmk, a caspase inhibitor, can suppress the Bcl-2-dependent cell survival at 39.5³C. This result suggests that a caspase-like activity can act as an inhibitor of apoptosis in this model, downstream of Bcl-2. Our results also suggest that this activity may be up-regulated by Bcl-2 and may be responsible for cleavage of the tumor suppressor Rb protein.