Table 7.
The effect of several drugs on IMV and EEV entrya
Drug concentration | Target | IMV (%) | EEV (%) |
---|---|---|---|
Pertussis toxin (500 ng/ml) | Trimeric G | 100b | 100b |
Cholera toxin (500 ng/ml) | Trimeric G | 100 | 100 |
Alf4− | Trimeric G | 100 | 100 |
Wortmannin (0.5 μM) | PI3 kinase | 100 | 100 |
PMA (100 nM) | PKC | 50 | 100 |
Staurosporin (200 nM) | PK | 39 | 100 |
Calphostin C (250 nM) | PKC | 30 | 100 |
BIS (10 μM) | PKC | 60 | 100 |
Genistein (25 μM) | PTK | 65 | 100 |
Genistein (200 μM) | PTK | 31 | 77 |
Tyrphostin 23 (25 μM) | PTK | 57 | 100 |
Tyrphostin 23 (100 μM) | PTK | 28 | 80 |
Myr. A (500 nM) | PKA | 100 | 100 |
U73122 (20 μM) | PLC | 100 | 100 |
Target, the intracellular target of the drug; Trimeric G, trimeric G proteins; PKC, protein kinase C; PK, protein kinase; PTK, protein tyrosine kinase; PKA, protein kinase A; PLC, phospholipase C; Alf4−, aluminium fluoride; PMA, phorbol 12-myristate 13-acetate; BIS, Bisindolylmaleimide; Myr. A, myristoylated peptide mimicking the active site of protein kinase A.
In each case, 30 treated cells were counted and the amount is expressed as a percentage of the control, which consisted of untreated cells.