Fig. 5.
Fig. 5. Reconstitution of splenic CD8α+ and CD8α−DCs from CD4low lymphoid precursors. / Thymic CD4low precursors (3 × 104) from C57 BL/Ka Ly 5.2 donor mice were injected intravenously into γ-irradiated (7 Gy) C57 BL/6 Ly 5.1 Pep3b recipient mice, along with 4 × 104 Ly 5.1 BM cells to ensure survival of recipients. At the indicated times, mice were analyzed for donor-derived DCs, identified as Ly 5.2+ CD11c+cells, in splenic DC-enriched 1.061-density fractions. The percentage of Ly5.2− and Ly5.2+ CD11c+ DCs (contour plots), as well as the percentage of CD8α− and CD8α+ DCs among Ly5.2+ DCs (black histograms) are indicated. Grey profiles show the expression of CD4 and F4/80 by CD8α− DCs. White profiles represent control stainings. These results are representative of four independent experiments with similar results.

Reconstitution of splenic CD8α+ and CD8αDCs from CD4low lymphoid precursors.

Thymic CD4low precursors (3 × 104) from C57 BL/Ka Ly 5.2 donor mice were injected intravenously into γ-irradiated (7 Gy) C57 BL/6 Ly 5.1 Pep3b recipient mice, along with 4 × 104 Ly 5.1 BM cells to ensure survival of recipients. At the indicated times, mice were analyzed for donor-derived DCs, identified as Ly 5.2+ CD11c+cells, in splenic DC-enriched 1.061-density fractions. The percentage of Ly5.2 and Ly5.2+ CD11c+ DCs (contour plots), as well as the percentage of CD8α and CD8α+ DCs among Ly5.2+ DCs (black histograms) are indicated. Grey profiles show the expression of CD4 and F4/80 by CD8α DCs. White profiles represent control stainings. These results are representative of four independent experiments with similar results.

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