As described recently in more detail [44], the CellTiter-GloTM Luminescent Cell Viability Assay, generating a luminescent signal,

is based on quantification of the cellular ATP levels. Tests were performed at least in quadruplicates. Luminescence was measured in the Wallac 1420 Victor, a microplate luminescence reader. Each point represents the mean ±SD PRIMA-1MET (bars) of replicates from at least four experiments. Determination of Caspase-3/7 Activity The activity of both caspases was determined using the APO-ONE Homogenous Caspase-3/7 Assay (Promega, Madison, WI) which uses the caspase-3/7 substrate rhodamine 110, bis-(N-CBZ-L-aspartyl-L-glutamyl-L-valyl-L-aspartic acid amide) (Z-DEVD-R100) as described previously [44]. Briefly, rat cells were plated in 96-well microtiter plates. One day after plating the cells were exposed for 24 h to increasing drug concentrations.

Thereafter, culture supernatant was transferred into another microtiter plate to separately determine the caspase activity in cells and in culture medium. Then selleck products an equal volume of caspase substrate was added and samples were incubated at 37°C for different periods of time to assess the best signal-to-background ratio. The fluorescence was measured at 485 nm. Luminescence and fluorescence were measured in the Wallac 1420 Victor, a microplate luminescence reader. Each point represents the mean ± SD (bars) of replicates from at least three experiments. Measurement of the DNA Content of Single Cells by Flow Cytometry The measurement of DNA content was performed by flow cytometric analysis based on a slightly out modified method [38] described previously [36]. The cells were detached from substratum by trypsinization, and then all cells were harvested by centrifugation and washed in PBS. Aliquots of 1 × 106 cells were used for further analysis.

Cells were stained with propidium iodide (PI) as described, previously [39]. Fluorescence was measured using the Becton Dickinson ACY-1215 price FACScan after at least 2 h incubation of the cells at +4°C in the dark. Results Differential Proliferation Rate of y and o Immortalized Rat Cells In the first step the proliferation rate of primary rat cells and four studied cell clones were determined. Cells plated in the defined cell density were cultivated for 5 days at a basal temperature. Cell numbers were determined in 12 h intervals by two different methods. First, cells were counted using an automatic cell counter and in parallel numbers of living cells were determined by the CellTiter-GloTM Luminescent Cell Viability Assay (Promega Corporation, Madison, WI).