WORTMANNIN AND ITS STRUCTURAL ANALOG DEMETHOXYVIRIDIN INHIBIT STIMULATED PHOSPHOLIPASE A(2) ACTIVITY IN SWISS 3T3 CELLS - WORTMANNIN IS NOTA SPECIFIC INHIBITOR OF PHOSPHATIDYLINOSITOL 3-KINASE
Mj. Cross et al., WORTMANNIN AND ITS STRUCTURAL ANALOG DEMETHOXYVIRIDIN INHIBIT STIMULATED PHOSPHOLIPASE A(2) ACTIVITY IN SWISS 3T3 CELLS - WORTMANNIN IS NOTA SPECIFIC INHIBITOR OF PHOSPHATIDYLINOSITOL 3-KINASE, The Journal of biological chemistry, 270(43), 1995, pp. 25352-25355
Wortmannin and its structural analogue demethoxy-viridin (DMV) have be
en reported to be specific inhibitors of phosphatidylinositol 3-kinase
activity. Here we report that these compounds are not as selective as
assumed and demonstrate inhibition of bombesin stimulated phospholipa
se A(2) activity by both wortmannin and DMV with an IC50 (2 nM) which
is slightly more potent than the inhibition of insulin-stimulated phos
phatidylinositol 3,4,5-trisphosphate generation in these cells (simila
r to 10 nM). While it has not been possible to fully block in vitro ph
ospholipase A(2) activity with wortmannin, inhibition cannot be a cons
equence of inhibition of PI 3-kinase activity since bombesin fails to
generate 3-phosphorylated lipids in the intact cell. Therefore, while
wortmannin is indeed a PI S-kinase inhibitor, it is not as specific as
previously reported, and experimental conclusions based solely on its
use should be treated with caution.