Fig. 7.
Fig. 7. Kinetics of splenic DC differentiation and phenotypic variations of CD8α− DCs during reconstitution after transfer of BM cells. / BM cells (2 × 106) 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. At the indicated times, mice were analyzed for donor-derived DCs 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 Ly5.2+CD8α− DCs; the percentage of CD4+ or F4/80+ cells is indicated. White profiles represent control stainings. These results are representative of three independent experiments with similar results.

Kinetics of splenic DC differentiation and phenotypic variations of CD8α DCs during reconstitution after transfer of BM cells.

BM cells (2 × 106) 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. At the indicated times, mice were analyzed for donor-derived DCs 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 Ly5.2+CD8α DCs; the percentage of CD4+ or F4/80+ cells is indicated. White profiles represent control stainings. These results are representative of three independent experiments with similar results.

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