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. 2019 Dec 6;2019:5637075. doi: 10.1155/2019/5637075

Figure 5.

Figure 5

Analysis of cell death in both hiPSC-RPE Control and AMD cells during oxidative stress exposure. Quantification by an MTT test of cell death induced by Fe-NTA treatment during 24 hours in both (a–c) hiPSC-RPE Control (N = 6) and (b, c) AMD (N = 6) cells (triplicate per cell line). Statistical analysis: one-way ANOVA, post hoc Dunnett and two-way ANOVA, and post hoc Bonferroni. p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.0001. (c) Flow cytometry analysis and (b) quantification of cell death pathway using annexin-V PI staining. Control (N = 4) and AMD (N = 6) (one analysis per cell line). Comparison of each dose between hiPSC-RPE Control and AMD cells for each dose. Control cells (N = 6) and AMD cells (N = 6) (triplicate per cell line). Statistical analysis: two-way ANOVA and post hoc Bonferroni. p < 0.05, ∗∗p < 0.01, and ∗∗∗p < 0.0001.