1. Transfection of the Stable Cell Line with the Inducible Expression Vector System
- Seed human embryonic kidney (HEK)293 cells stably expressing green fluorescent protein (GFP) or GFP-CaeB in a 12-well plate at a density of 1 x 105 cells/well.
- 19 hr post-seeding, co-transfect the cells with the regulator plasmid and response plasmid, either encoding Bax or activated caspase 3.
- Co-transfect the stable HEK293 cells with 100 ng of pWHE125-P regulator plasmid (Figure 1) and 100 ng of the response plasmids pWHE655-hBax or pWHE655-revCasp3 (Figure 2) and 0.4 µl of polyethylenimine.
- Prepare the deoxyribonucleic acid (DNA) and polyethylenimine transfection reagent each in 75 µl of Opti-MEM medium and incubate for exactly 5 min at room temperature (RT). For complex formation, incubate both mixtures together for 15 min at RT.
- Add the polyethylenimine/DNA solution dropwise to the cells and incubate at 37 °C in 5% CO2.
2. Induction of Apoptosis
- 5 hr post-transfection, induce expression of the pro-apoptotic proteins by the addition of 1 µg/ml doxycycline to the culture medium. Incubate cells for 18 hr at 37 °C in 5% CO2.