Figure 5.
Modulation of FOXO3 and TP53 expression in p21−/−/Hbbth3/+ erythroid cells. (Ai) FOXO3 nuclear localization in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 40 cells (quantification, right graph). Scale bar: 5 μm. (Aii) TP53 nuclear localization in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 40 cells (quantification, right graph). Scale bar: 5 μm. (B) Histograms of Mitotracker Green staining of TER119+ cells in different gates (left) and quantification (right). (C) Mitochondrial morphology in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 30 cells. Scale bar: 5 μm. Quantification of mitochondrial area (top). Results are shown as mean ± standard error of the mean; ∗P < .05; ∗∗P < .01; ∗∗∗P < .001; ∗∗∗∗P < .0001; and n.s., not significant.

Modulation of FOXO3 and TP53 expression in p21−/−/Hbbth3/+ erythroid cells. (Ai) FOXO3 nuclear localization in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 40 cells (quantification, right graph). Scale bar: 5 μm. (Aii) TP53 nuclear localization in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 40 cells (quantification, right graph). Scale bar: 5 μm. (B) Histograms of Mitotracker Green staining of TER119+ cells in different gates (left) and quantification (right). (C) Mitochondrial morphology in erythroid progenitors from WT, p21−/−, Hbbth3/+, and p21−/−/Hbbth3/+ mice using confocal microscopy; analyses of at least 30 cells. Scale bar: 5 μm. Quantification of mitochondrial area (top). Results are shown as mean ± standard error of the mean; ∗P < .05; ∗∗P < .01; ∗∗∗P < .001; ∗∗∗∗P < .0001; and n.s., not significant.

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