Fig. 5.
Fig. 5. The in vivo effects of IL-7 on TREC generation in NOD-SCID-hu mice. / Four weeks after implantation of human fetal thymus and liver, NOD-SCID-hu mice were treated with 100 ng IL-7 twice daily for 10 days. Seven (control, n = 3; IL-7, n = 4) and 21 days (control, n = 5; IL-7, n = 7) after the last injection, the grafts, spleen, and PBMCs were recovered from the mice for phenotypic analysis and TRECs. The upper panels of panel A indicate percentage of human CD3+cells and the panels in the middle row of panel A indicate human CD4+ and CD8+ expression on the CD3+ population of PBMC (left) and spleen (right). The bottom figures of panel A show CD45RA+ cells on CD3+CD4+ or CD3+CD8+populations of PBMCs (left) and spleen (right). The TREC levels of grafts and the graft weights in control and IL-7–treated mice are shown in panels B and C, respectively. The percentages of Ki67+ cells in each subpopulation of grafts are shown in panel D.

The in vivo effects of IL-7 on TREC generation in NOD-SCID-hu mice.

Four weeks after implantation of human fetal thymus and liver, NOD-SCID-hu mice were treated with 100 ng IL-7 twice daily for 10 days. Seven (control, n = 3; IL-7, n = 4) and 21 days (control, n = 5; IL-7, n = 7) after the last injection, the grafts, spleen, and PBMCs were recovered from the mice for phenotypic analysis and TRECs. The upper panels of panel A indicate percentage of human CD3+cells and the panels in the middle row of panel A indicate human CD4+ and CD8+ expression on the CD3+ population of PBMC (left) and spleen (right). The bottom figures of panel A show CD45RA+ cells on CD3+CD4+ or CD3+CD8+populations of PBMCs (left) and spleen (right). The TREC levels of grafts and the graft weights in control and IL-7–treated mice are shown in panels B and C, respectively. The percentages of Ki67+ cells in each subpopulation of grafts are shown in panel D.

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