Fig. 3.
Fig. 3. Reconstitution of LCs and DDCs from CD4lowprecursors. / Thymic CD4low precursors (3 × 104) were injected IV into 7 Gy γ-irradiated 8-week-old C57 BL/6 Ly 5.1 Pep3b recipient mice, along with 4 × 104 Ly 5.1 BM cells to ensure survival of recipients. Mice were exposed to UV-C irradiation for 30 minutes, 24 hours after transfer of CD4low precursors. Control mice were injected with 4 × 104 Ly 5.1 BM cells. At the indicated times mice were analyzed for donor-derived Ly 5.2 LCs or DDCs. The phenotype of Ly 5.2+ LCs reconstituted from CD4low precursors 2 weeks after transfer is shown. The percentage of Ly 5.2+and Ly 5.2− MHC II+ LCs and DDCs is indicated. These results are representative of 3 experiments with similar results.

Reconstitution of LCs and DDCs from CD4lowprecursors.

Thymic CD4low precursors (3 × 104) were injected IV into 7 Gy γ-irradiated 8-week-old C57 BL/6 Ly 5.1 Pep3b recipient mice, along with 4 × 104 Ly 5.1 BM cells to ensure survival of recipients. Mice were exposed to UV-C irradiation for 30 minutes, 24 hours after transfer of CD4low precursors. Control mice were injected with 4 × 104 Ly 5.1 BM cells. At the indicated times mice were analyzed for donor-derived Ly 5.2 LCs or DDCs. The phenotype of Ly 5.2+ LCs reconstituted from CD4low precursors 2 weeks after transfer is shown. The percentage of Ly 5.2+and Ly 5.2 MHC II+ LCs and DDCs is indicated. These results are representative of 3 experiments with similar results.

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