Figure 1
Figure 1. Mac1+Gr1+ cells in the thymus are C/EBPα dependent and show polynuclear morphology. (A) Gating of Mac1+Gr1+ granulocytes in the adult mouse thymus and spleen. (B) Sorted Mac1+Gr1+ cells in the thymus and CD4/CD8 double-negative (DN) T-lymphocytes were cytospun and examined by Wright-Giemsa stain at 100×. Scale bars represent 10 μm. (C) The development of total CD4+ thymocytes and thymic granulocytes was examined in mixed chimeras of C/EBPαF/F;VavCre+ fetal liver or C/EBPαF/FVavCre− control fetal liver and congenic CD45.1+ BM. Two mice per group were examined 10 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (D) B cells and granulocyte development in the spleen were examined in mixed chimeras of C/EBPαF/F;VavCre+ fetal liver and congenic CD45.1+ BM. Two mice per group were examined 8-10 weeks after reconstitution.

Mac1+Gr1+ cells in the thymus are C/EBPαdependent and show polynuclear morphology. (A) Gating of Mac1+Gr1+ granulocytes in the adult mouse thymus and spleen. (B) Sorted Mac1+Gr1+ cells in the thymus and CD4/CD8 double-negative (DN) T-lymphocytes were cytospun and examined by Wright-Giemsa stain at 100×. Scale bars represent 10 μm. (C) The development of total CD4+ thymocytes and thymic granulocytes was examined in mixed chimeras of C/EBPαF/F;VavCre+ fetal liver or C/EBPαF/FVavCre control fetal liver and congenic CD45.1+ BM. Two mice per group were examined 10 weeks after reconstitution of lethally irradiated CD45.1+ hosts. (D) B cells and granulocyte development in the spleen were examined in mixed chimeras of C/EBPαF/F;VavCre+ fetal liver and congenic CD45.1+ BM. Two mice per group were examined 8-10 weeks after reconstitution.

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