Figure 2.
Figure 2. Expansion of immature erythroid cells in Lyn-/- spleen and increased erythroid CFU-e numbers in BM and spleen of Lyn-/- mice. (A) A 3-color flow cytometric analysis of 8-week-old Lyn+/+ and Lyn-/- spleen populations stained with CD71 and Ter119. Propidium iodide (PI)-positive and mature RBCs were excluded from the analysis. Relative percentages (± SD) of immature erythroid (upper right quadrant) and more mature erythroid (lower right) cells of 3 mice of each genotype are indicated. Erythropoiesis in (B) spleen, (C) BM of 8- and 16-week-old Lyn+/+ and Lyn-/- mice, and (D) embryonic day-14 fetal liver was assessed by methylcellulose culture. Mature erythroid (CFU-e) and immature erythroid (BFU-e) progenitors were determined at day 2 and day 10, respectively. (E) Relative percentages (± SD) of annexin-FITC-positive erythroid cells in fetal liver (n = 7-8/genotype) and adult bone marrow (n = 5/genotype) are indicated.

Expansion of immature erythroid cells in Lyn-/- spleen and increased erythroid CFU-e numbers in BM and spleen of Lyn-/- mice. (A) A 3-color flow cytometric analysis of 8-week-old Lyn+/+ and Lyn-/- spleen populations stained with CD71 and Ter119. Propidium iodide (PI)-positive and mature RBCs were excluded from the analysis. Relative percentages (± SD) of immature erythroid (upper right quadrant) and more mature erythroid (lower right) cells of 3 mice of each genotype are indicated. Erythropoiesis in (B) spleen, (C) BM of 8- and 16-week-old Lyn+/+ and Lyn-/- mice, and (D) embryonic day-14 fetal liver was assessed by methylcellulose culture. Mature erythroid (CFU-e) and immature erythroid (BFU-e) progenitors were determined at day 2 and day 10, respectively. (E) Relative percentages (± SD) of annexin-FITC-positive erythroid cells in fetal liver (n = 7-8/genotype) and adult bone marrow (n = 5/genotype) are indicated.

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