Figure 4
Figure 4. Preserved development of αβ lineage T cells in the absence of Maml1. (A) Flow cytometric analysis showed a similar percentage of CD4+CD8+ double-positive and CD4+ or CD8+ single-positive thymocytes in recipients of Maml1−/− compared with Maml1+/− progenitors. Numbers indicate the percentage of cells in each quadrant. Host-derived CD45.1+ cells were excluded from the analysis. (B) Normal distribution of Lin− thymocyte progenitor subsets, as defined using c-Kit and CD25 expression, in recipients of Maml1−/− compared with Maml1+/− progenitors. Numbers indicate the percentage of cells in each quadrant. Host-derived CD45.1+ cells were excluded from the analysis. (C) Absolute number of donor-derived double-positive thymocytes in all the fetal liver chimeras that were analyzed (Maml1+/−, ▵, n = 21; Maml1−/−, ▴, n = 9). The trend for decreased numbers of double-positive thymocytes in Maml1−/− compared with Maml1+/− progenitors was not statistically significant (P = .14; Student t test).

Preserved development of αβ lineage T cells in the absence of Maml1. (A) Flow cytometric analysis showed a similar percentage of CD4+CD8+ double-positive and CD4+ or CD8+ single-positive thymocytes in recipients of Maml1−/− compared with Maml1+/− progenitors. Numbers indicate the percentage of cells in each quadrant. Host-derived CD45.1+ cells were excluded from the analysis. (B) Normal distribution of Lin thymocyte progenitor subsets, as defined using c-Kit and CD25 expression, in recipients of Maml1−/− compared with Maml1+/− progenitors. Numbers indicate the percentage of cells in each quadrant. Host-derived CD45.1+ cells were excluded from the analysis. (C) Absolute number of donor-derived double-positive thymocytes in all the fetal liver chimeras that were analyzed (Maml1+/−, ▵, n = 21; Maml1−/−, ▴, n = 9). The trend for decreased numbers of double-positive thymocytes in Maml1−/− compared with Maml1+/− progenitors was not statistically significant (P = .14; Student t test).

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