Figure 2
Figure 2. Telomere dysfunction in HSCs and the thymic epithelium has minor effects on the impairment in thymopoiesis. (A-D) Two- to 3-month-old mTerc+/+ or G3mTerc−/− recipient mice were lethally irradiated and reconstituted with the bone marrow (1.5 × 106 cells) of 12-month-old G3mTerc−/− or mTerc+/+ donor mice (n = 6 recipients per group). At 3 to 5 months after bone marrow transplantation, neonatal thymi from mTerc+/+ mice or G3mTerc−/− mice were transplanted under the kidney capsules of the recipient mice. Grafted thymi were analyzed at 2 to 3 months after thymus transplantation. (A) Experimental scheme. (B-D) Analysis of the grafted thymi. The bar graphs show (B) the percentage of CD4 and CD8 double-positive thymocytes, (C) the thymus weight, and (D) the total number of thymocytes. Error bars represent SD in all panels.

Telomere dysfunction in HSCs and the thymic epithelium has minor effects on the impairment in thymopoiesis. (A-D) Two- to 3-month-old mTerc+/+ or G3mTerc−/− recipient mice were lethally irradiated and reconstituted with the bone marrow (1.5 × 106 cells) of 12-month-old G3mTerc−/− or mTerc+/+ donor mice (n = 6 recipients per group). At 3 to 5 months after bone marrow transplantation, neonatal thymi from mTerc+/+ mice or G3mTerc−/− mice were transplanted under the kidney capsules of the recipient mice. Grafted thymi were analyzed at 2 to 3 months after thymus transplantation. (A) Experimental scheme. (B-D) Analysis of the grafted thymi. The bar graphs show (B) the percentage of CD4 and CD8 double-positive thymocytes, (C) the thymus weight, and (D) the total number of thymocytes. Error bars represent SD in all panels.

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