Figure 3
Figure 3. Inhibition of erythroid differentiation of Hri−/− mice during iron deficiency and apoptosis of splenic Ter119+ erythroblasts in iron deficiency. (A) Erythroid differentiation of the spleen of Hri+/+ and Hri−/− adult mice maintained on a normal diet or an iron-restricted diet. (B) Benzidine-Giemsa–stained cells from sorted P3 and P4+P5 populations. Images were taken with 40× objective using Leitz microscope equipped with Pixelink digital imaging system. (C) Density plots of apoptosis of Ter119+ erythroblasts. Splenic Ter119+ erythroid cells were gated first. Apoptosis of these cells was then analyzed by their CD71 expression and AnV binding. (D) Quantitation of percentages of AnV+ cells in CD71+Ter119+ cells only. Data are presented as mean ± SD (n = 3 for each group of mice; **P < .01).

Inhibition of erythroid differentiation of Hri−/− mice during iron deficiency and apoptosis of splenic Ter119+ erythroblasts in iron deficiency. (A) Erythroid differentiation of the spleen of Hri+/+ and Hri−/− adult mice maintained on a normal diet or an iron-restricted diet. (B) Benzidine-Giemsa–stained cells from sorted P3 and P4+P5 populations. Images were taken with 40× objective using Leitz microscope equipped with Pixelink digital imaging system. (C) Density plots of apoptosis of Ter119+ erythroblasts. Splenic Ter119+ erythroid cells were gated first. Apoptosis of these cells was then analyzed by their CD71 expression and AnV binding. (D) Quantitation of percentages of AnV+ cells in CD71+Ter119+ cells only. Data are presented as mean ± SD (n = 3 for each group of mice; **P < .01).

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