This video demonstrates a nuclear staining method to detect the cytotoxic effect of mitocan on drug-sensitive cancer cells and healthy variants. The double staining with DNA-binding dyes such as propidium iodide and Hoechst dye provides a clear distinction between the dead and live cells, thus helping to assess the cytotoxicity of the drug.
Protocol
1. Cytotoxicity Assay: Setup Prepare solutions of compounds of interest at desired concentrations in the appropriate media (serum-free or 1, 2.5, or 5% FBS RPMI-1640). To measure the cytotoxicity of a single compound (e.g., to determine effective doses), prepare compounds at 2x final concentration. To measure the cytotoxicity of compound combinations, prepare compounds at 4x final concentration. Prepare solvent-only controls by mixing the same amount of solvent with the appro…
Disclosures
The authors have nothing to disclose.
Materials
2-Deoxy-D-glucose/2-DG
Chem-Impex
50-519-067
3-bromo-pyruvate
Alfa Aesar
1113-59-3
96-Well plates
Greiner Bio-One
655090
Black or clear flat-bottomed 96-well plates
Countess II automated cell counter
Thermo Fisher
Cytation 5 Cell Imaging Multi-Mode Reader
BioTek
Hoechst 33342
Thermo Fisher
62249
20 mM solution; final concentration 1:1,000
HyClone fetal bovine serum
GE Healthcare
#25-514
m-chlorophenylhydrazone/CCCP
Sigma Aldrich
C2759
PBS tablets
Thermo Fisher
BP2944100
1 tablet + 200 mL of sterile water = 1x PBS solution
Penicillin-Streptomycin-Glutamine (100X)
Gibco
10378016
Propidium Iodide
Thermo Fisher
50-596-072
Dry powder; stock 1 mg/mL in PBS; final concentration 5 µg/mL (leukemia cells), 1 µg/mL (normal PBMCs)
Rotenone
Ark Pharm
AK115691
RPMI-1640 Medium With L-glutamine and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture
Differential Nuclear Staining Assay: An Assay to Determine Mitocan Cytotoxicity by Propidium Iodide and Hoechst Double Staining. J. Vis. Exp. (Pending Publication), e21178, doi: (2023).