Both methods gave comparable results within the first 3 days; later CellTitert-Glo underestimated the numbers of transformed cells. The primary cells selleck kinase inhibitor isolated from rat embryos (RECs) at gestation day 13.5 (y) grew much slower than those isolated at day 15.5 (o) [30]. The population doubling time (PDT) calculated from growth curves for the oRECs was approximately 2-fold shorter than that for yRECs (Table 1). Table 1 Comparison of the values of the population doubling times (PDTs) Cells Age of RECs Overexpressed proteins PDT [h] Rat embryonal cells (RECs) yRECs 13.5 gd – 85.8 oRECs LCZ696 solubility dmso 15.5 gd – 44.8 Cell clones 402/534 13.5 gd p53 135Val 32.07 602/534 15.5 gd p53 135Val

14.20 189/111 13.5 gd p53 135Val c-Ha-Ras 11.52 173/1022 15.5 gd p53 135V\al c-Ha-Ras 11.16 The increase of the cell numbers within the time period between 24 h and 48 h after plating was used for determination of the PDT RECs transfected with ts p53135Val mutant alone, or simultaneously with human c-Ha-RAS, generated immortalized and transformed cells, respectively. As described previously [30], JNK-IN-8 chemical structure the phenotype of immortalized cells resembled that of primary cells. However, in contrast to RECs, cells

expressing ts p53135Val got over the Hayflick limit and did not undergo senescence. Cotransfection with c-Ha-RAS resulted in a clear change of cell morphology to spindle-shaped [30] and conferred the generated cell lines a high mitotic potential. The features of transformed cells were also functionally proved. After subcutaneous injection of cells overexpressing p53135Val +c-Ha-Ras into rats large tumors appeared within approximately 2 weeks [30]. As shown in Fig. 1, the transformed cells Protein tyrosine phosphatase divided very rapidly. Interestingly, the immortalized and transformed

cell lines originating from oRECs (clone 602/534 and 173/1022), divided at 37°C much more rapidly than those from yRECs (clone 402/534 and 189/111). The population doubling time (PDT) was calculated for each cell clone from the growth curves. As depicted in Table 1, even immortalization of yRECs with ts p53135Val mutant (clone 402/534) did not confer them high mitotic potential at non-permissive temperature. On the other hand, the proliferative potential of their counterparts generated from oRECs was markedly higher. Interestingly, the same trend was observed in transformed cell lines after co-transfection with c-Ha-RAS. However, during the time period between 24 h and 48 h after cell plating, the transformed cells did not gain the full dividing capacity. The difference in the proliferation rate between transformed y and o cell clones became evident 48 h after cell plating (Fig. 1). Fig. 1 Kinetics of proliferation of immortalized and transformed rat cells. Immortalized (402/534 and 602/534) and transformed (189/111 and 173/1022) cell clones established in RECs from embryos at 13.5 (y) and 15.5 (o) gestation days were examined.