Fig. 3.
Fig. 3. Effect of Spi-B on development of pDCs. / CD34+CD38− fetal liver (A) or CD34+CD1a− postnatal thymus (B) were transduced with LZRS Spi-B-IRES-GFP, LZRS ΔSpi-B-IRES-GFP, or with control-IRES-GFP and incubated with S17 cells for 5 to 7 days for postnatal thymocytes and fetal liver cells, respectively. The quadrants were placed to include 99% of the cells stained with control antibodies. The cell recoveries of all samples were the same; thus, the differences in percentages of pDCs indicated in the figure reflect the differences in absolute numbers of pDCs generated in this system.

Effect of Spi-B on development of pDCs.

CD34+CD38 fetal liver (A) or CD34+CD1a postnatal thymus (B) were transduced with LZRS Spi-B-IRES-GFP, LZRS ΔSpi-B-IRES-GFP, or with control-IRES-GFP and incubated with S17 cells for 5 to 7 days for postnatal thymocytes and fetal liver cells, respectively. The quadrants were placed to include 99% of the cells stained with control antibodies. The cell recoveries of all samples were the same; thus, the differences in percentages of pDCs indicated in the figure reflect the differences in absolute numbers of pDCs generated in this system.

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