Figure 4
Figure 4. Ccbe1lacZ/lacZ fetal livers exhibit a specific defect in erythropoiesis. (A) Erythroblast maturation in Ccbe1lacZ/lacZ and control fetal livers was assessed by staining for CD71 and Ter119 at E13.5. Note that the number of erythroblasts in the Ccbe1lacZ/lacZ fetal liver was reduced at all stages of maturation. (B) Erythroblast maturation in Ccbe1lacZ/lacZ and control fetal livers was also assessed by staining for CD44 and Ter119 at E13.5. (C) The fraction of Ter119+ erythroblasts in Ccbe1lacZ/lacZ fetal livers is reduced at E13.5. (D) The fraction of CD45+Ter119− cells in Ccbe1lacZ/lacZ fetal livers is unchanged at E13.5. (E) Ccbe1lacZ/lacZ fetal livers have normal numbers of Lin-cKit+Sca1+ hematopoietic stem cells at E13.5. (E-N) Ccbe1lacZ/lacZ fetal livers have normal numbers of E-cadherin+ hepatocytes (F,G), LYVE1+ sinusoidal endothelial cells (H,I), PDGFRb+ vascular pericytes (J,K), vWF+ megakaryocytes (L,M), and Desmin+ stellate cells (N,O). Scale bars represent 25 μm.

Ccbe1lacZ/lacZ fetal livers exhibit a specific defect in erythropoiesis. (A) Erythroblast maturation in Ccbe1lacZ/lacZ and control fetal livers was assessed by staining for CD71 and Ter119 at E13.5. Note that the number of erythroblasts in the Ccbe1lacZ/lacZ fetal liver was reduced at all stages of maturation. (B) Erythroblast maturation in Ccbe1lacZ/lacZ and control fetal livers was also assessed by staining for CD44 and Ter119 at E13.5. (C) The fraction of Ter119+ erythroblasts in Ccbe1lacZ/lacZ fetal livers is reduced at E13.5. (D) The fraction of CD45+Ter119 cells in Ccbe1lacZ/lacZ fetal livers is unchanged at E13.5. (E) Ccbe1lacZ/lacZ fetal livers have normal numbers of Lin-cKit+Sca1+ hematopoietic stem cells at E13.5. (E-N) Ccbe1lacZ/lacZ fetal livers have normal numbers of E-cadherin+ hepatocytes (F,G), LYVE1+ sinusoidal endothelial cells (H,I), PDGFRb+ vascular pericytes (J,K), vWF+ megakaryocytes (L,M), and Desmin+ stellate cells (N,O). Scale bars represent 25 μm.

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