On of the system is that highthroughput testing is not possible because only four experiments can be performed in parallel. The endothelial cells EAhy 926 can be DprE1-IN-2 site exposed to relatively high concentrations (100 mg/ml) of 20 nm PPS for 24 hours without showing any apparent damage in a conventional culture. In microcarrier culture, the resistance to the toxic action of PPS is even higher. Two mechanisms could be suggested that may explain the lower cytotoxicity of PPS in microcarrier culture: a more physiological growth with a better supply of nutrients and the fact that a smaller area of the cell membrane is accessible to the PPS because cells are more densely packed [40]. Upon longer incubation times, however, the situation is inversed. The low concentrations of the NPs did not have a strong influence on the proliferation of cells maintained in conventional cell culture, but pronounced cytotoxicity was detected in microcarrier culture. This difference may be caused by a higher dilution of the intracellular concentration of NPs due to proliferation. Our experiments proved that the doubling rate of EAhy 926 cells in conventional get K162 culture was 2.3 times higher than in the microcarrier culture. At concentrations higher than 100 mg/ml, 20 nm PPS decreased the metabolic activity of the cells in conventional culture and inducedthe activation of caspases 3 and 7. In addition, an increased release of LDH, as an indicator of membrane damage, was also observed after exposure to these doses of PPS for 24 hours. Particles of 200 nm did not exert any effect upon culturing under the same conditions. Upon acute exposure, the main modes of PPS induced cell death were found to be apoptosis and necrosis. Frohlich et al. ?investigated the impacts of 20 nm carboxylated polystyrene (CPS) NPs in the same cell line, grown in conventional cell culture for 24 hours, and also demonstrated induction of necrosis and apoptosis [41]. This similarity between 20 nm CPS and 20 nm PPS may be linked to their similar physicochemical parameters: the differences in size (42 nm (CPS) vs. 73 nm (PPS)) were small and the surface charge of both particles was slightly negative. Upon prolonged exposure to PPS, not only LDH release was increased as compared to controls, but also the activation of caspases. However, it is very unlikely that both modes of cell death are induced at the same time. The contradictory findings on caspase activation (Fig. 6 A) could be explained by the normalization of very small differences in assay values (caspase 3/7) between untreated and treated cells versus larger differences in total cell numbers of the respective culture. Moreover, all other data supported the induction of necrosis as the predominant mode of action of 20 nm PPS upon long-term exposure. Collectively, we detected no induction of apoptosis and only low induction of necrosis at each time-point in cells 1326631 exposed to 20 mg/ml of 20 nm PPS. As both cell death mechanisms should occur within 24 hours [42], we presume that the reduction in cell number observed upon long-term exposure was also caused by the decreased cell proliferation in the BioLevitatorTM, as the lower doubling rateLong-Term Effects of Nanoparticlesof the cells in microcarrier cultures promotes the accumulation of NPs. The BioLevitatorTM bioreactor used in this study, also appears suitable for the assessment of biological effects upon exposure to other NMs. CNTs could find broad medical application, particularly in imaging and tr.On of the system is that highthroughput testing is not possible because only four experiments can be performed in parallel. The endothelial cells EAhy 926 can be exposed to relatively high concentrations (100 mg/ml) of 20 nm PPS for 24 hours without showing any apparent damage in a conventional culture. In microcarrier culture, the resistance to the toxic action of PPS is even higher. Two mechanisms could be suggested that may explain the lower cytotoxicity of PPS in microcarrier culture: a more physiological growth with a better supply of nutrients and the fact that a smaller area of the cell membrane is accessible to the PPS because cells are more densely packed [40]. Upon longer incubation times, however, the situation is inversed. The low concentrations of the NPs did not have a strong influence on the proliferation of cells maintained in conventional cell culture, but pronounced cytotoxicity was detected in microcarrier culture. This difference may be caused by a higher dilution of the intracellular concentration of NPs due to proliferation. Our experiments proved that the doubling rate of EAhy 926 cells in conventional culture was 2.3 times higher than in the microcarrier culture. At concentrations higher than 100 mg/ml, 20 nm PPS decreased the metabolic activity of the cells in conventional culture and inducedthe activation of caspases 3 and 7. In addition, an increased release of LDH, as an indicator of membrane damage, was also observed after exposure to these doses of PPS for 24 hours. Particles of 200 nm did not exert any effect upon culturing under the same conditions. Upon acute exposure, the main modes of PPS induced cell death were found to be apoptosis and necrosis. Frohlich et al. ?investigated the impacts of 20 nm carboxylated polystyrene (CPS) NPs in the same cell line, grown in conventional cell culture for 24 hours, and also demonstrated induction of necrosis and apoptosis [41]. This similarity between 20 nm CPS and 20 nm PPS may be linked to their similar physicochemical parameters: the differences in size (42 nm (CPS) vs. 73 nm (PPS)) were small and the surface charge of both particles was slightly negative. Upon prolonged exposure to PPS, not only LDH release was increased as compared to controls, but also the activation of caspases. However, it is very unlikely that both modes of cell death are induced at the same time. The contradictory findings on caspase activation (Fig. 6 A) could be explained by the normalization of very small differences in assay values (caspase 3/7) between untreated and treated cells versus larger differences in total cell numbers of the respective culture. Moreover, all other data supported the induction of necrosis as the predominant mode
of action of 20 nm PPS upon long-term exposure. Collectively, we detected no induction of apoptosis and only low induction of necrosis at each time-point in cells 1326631 exposed to 20 mg/ml of 20 nm PPS. As both cell death mechanisms should occur within 24 hours [42], we presume that the reduction in cell number observed upon long-term exposure was also caused by the decreased cell proliferation in the BioLevitatorTM, as the lower doubling rateLong-Term Effects of Nanoparticlesof the cells in microcarrier cultures promotes the accumulation of NPs. The BioLevitatorTM bioreactor used in this study, also appears suitable for the assessment of biological effects upon exposure to other NMs. CNTs could find broad medical application, particularly in imaging and tr.