Figure 1
Immunologic status of 8- to 10-day-old TGF-β1−/− mice. (A) Analysis of CD4+ CD25+ expression in CD3 T cell of thymus, lymph node, and spleen cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. Histograms are the mean ± SD of 3 independent experiments, *P < .05. (B) Analysis of FOXP3 expression in CD4+CD25+ cells from spleen, lymph node, and thymus. The flow cytometric profiles are the representative histograms of 2 experiments (6 mice per experiment). (C) Analysis of the Lin− Sca-1+ c-Kit+ (LSK) population in BM cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. The flow cytometric profiles are representative of 3 independent experiments with 6 mice per experiment. (D) Analysis of the CD150+ CD48low (signaling lymphocyte activation molecule) population in LSK BM cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. The flow cytometric profiles are representative of 3 independent experiments with 6 mice per experiment, *P < .05. PE indicates phycoerythrin; Cy7, indocyanine 7.

Immunologic status of 8- to 10-day-old TGF-β1−/− mice. (A) Analysis of CD4+ CD25+ expression in CD3 T cell of thymus, lymph node, and spleen cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. Histograms are the mean ± SD of 3 independent experiments, *P < .05. (B) Analysis of FOXP3 expression in CD4+CD25+ cells from spleen, lymph node, and thymus. The flow cytometric profiles are the representative histograms of 2 experiments (6 mice per experiment). (C) Analysis of the Lin Sca-1+ c-Kit+ (LSK) population in BM cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. The flow cytometric profiles are representative of 3 independent experiments with 6 mice per experiment. (D) Analysis of the CD150+ CD48low (signaling lymphocyte activation molecule) population in LSK BM cells from 8- to 10-day-old TGF-β1+/+ and TGF-β1−/− mice. The flow cytometric profiles are representative of 3 independent experiments with 6 mice per experiment, *P < .05. PE indicates phycoerythrin; Cy7, indocyanine 7.

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