The

vital cell count observed after trypan blue staining is in good agreement with the one obtained by the Mossman assay (Table 1, only the data for 20 μM RV at after 24 hour of treatment are shown). Table 1 Vital cell count after trypan blue staining of cells treated with resveratrol (20 μM) for 24 hours. RV – Treated 3T6 Cells Sample Vital Non-Vital 1 27 3 2 32 2 3 28 3 4 30 3 Average cell mortality 8.7 ± 2.6% Figure 1 Cytotoxicity of resveratrol assessed by the Mossman assay. The bars report the percentage of viable cells after different times of exposure to the drug (24 hours: four bars to the left; 48 hours two bars to the right). The untreated control and the sample in DMSO at 48 hour are omitted since the data are virtually LEE011 identical to the ones obtained at 24 hours. Data reported Niraparib in upper panel refer to 3T6 cells while those shown

in the lower panel refer to HL60 cells. We also investigated the cytotoxic activity of RV on the tumor cells HL60: a human promyelocytic leukemia cell line. The results clarly show that RV can significantly inhibit the cell growth already at a concentration of 25 μM. Subsequently we assessed the level of cell mortality induced by Py infection: in this case we used the method of vital cell staining only with trypan blue. As a matter of fact, the MTT assay is informative of cell death deriving from membrane damage Ribonucleotide reductase and former data from our laboratory indicated that the plasma membrane is actually one of the targets of RV. On the contrary, trypan blue staining has a more general action ranging from a generic damage of cell membrane

to severe problems in cell Selleckchem PF299 homeostasis. Table 2 reports the vital cell counts in control and Py infected cells. Table 2 Assessment of the cell mortality rate due to Py proliferation. Virus Py 24 h Sample Vital Non-Vital 1 44 1 2 45 2 3 41 2 4 52 1 Average cell mortality 3,4% ± 1,5% Virus Py 48 h Sample Vital Non-Vital 1 40 2 2 46 4 3 44 4 4 49 2 Average cell mortality 6,7% ± 2,5% The vital cell count was evalutated by trypan blue staining. The reported data show that after 48 hours of infection the cell death rate is about as double as in controls: however the viral infection does not seem to cause extensive loss cell vitality. In the light of these results the effect of RV on Py proliferation was evaluated at 24 hours post-infection in cells were treated with 20 μM RV or at the concentrations of drug reported in the legends to the figures. Effect of resveratrol on the viral proliferation Semi-confluent cells were infected with Py and RV was added after the absorption phase at the indicated final concentrations. Infection was continued for 24 hours and progeny viral DNA was extracted according to the Hirt-procedure [26] (Figure 2A). The data clearly show that the viral replication is virtually abrogated at 20 μM RV.