Figure 5
Figure 5. Enhanced thymopoiesis in TGFβRIIlox/lox::Foxn1-Cre and recipient mice of HSCT early after irradiation. (A) Total thymic cellularity and (B) TEC cellularity in lethally irradiated recipients of T-cell–depleted bone marrow cells at different time points after transplantation (TEC cellularity of unconditioned mice that did not undergo transplantation was 0.42 × 106 ± 0.07 × 106 vs 0.41 × 106 ± 0.07 × 106, P > .05, for TGFβRIIlox/lox::Foxn1-Cre and TGFβRIIlox/lox, respectively). (C) The relative distribution of thymocytes according to CD4 and CD8 expression and (D) the absolute numbers of the 4 CD3−CD4−CD8− subpopulations (DN1-4) were determined in TGFβRIIlox/lox::Foxn1-Cre and TGFβRIIlox/lox mice 2 weeks after lethal irradiation (950 cGy) and transfer of 107 T cell–depleted bone marrow cells. Error bars represent SD, and percentages on plots in panel C are of total cells within gate.

Enhanced thymopoiesis in TGFβRIIlox/lox::Foxn1-Cre and recipient mice of HSCT early after irradiation. (A) Total thymic cellularity and (B) TEC cellularity in lethally irradiated recipients of T-cell–depleted bone marrow cells at different time points after transplantation (TEC cellularity of unconditioned mice that did not undergo transplantation was 0.42 × 106 ± 0.07 × 106 vs 0.41 × 106 ± 0.07 × 106, P > .05, for TGFβRIIlox/lox::Foxn1-Cre and TGFβRIIlox/lox, respectively). (C) The relative distribution of thymocytes according to CD4 and CD8 expression and (D) the absolute numbers of the 4 CD3CD4CD8 subpopulations (DN1-4) were determined in TGFβRIIlox/lox::Foxn1-Cre and TGFβRIIlox/lox mice 2 weeks after lethal irradiation (950 cGy) and transfer of 107 T cell–depleted bone marrow cells. Error bars represent SD, and percentages on plots in panel C are of total cells within gate.

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