Figure 4
Figure 4. Athymic nude mice develop CD4+/CD8+ T-ALLs when infused with ICN1-expressing cells. Survival curves are shown for cohorts of irradiated nude mice infused with noncultured ICN1+ bone marrow–derived cells (A; 5 mice/group; P = .03 by log-rank test), nonirradiated nude mice infused with ICN1+ bone marrow–derived cells after 12 days of culture (B; 9 Arf +/+, 8 Arf −/− recipient mice, P = .002), and nonirradiated nude mice infused with cultured ICN1+ thymus-derived cells (C; 3 mice/group, P = .02). Representative immunophenotypes of T-ALLs arising in each experiment are depicted in panels to the right of the corresponding survival curves (D-F). Although all leukemias had a dominant CD4+/CD8+ population, several also had CD8 single-positive subpopulations.

Athymic nude mice develop CD4+/CD8+ T-ALLs when infused with ICN1-expressing cells. Survival curves are shown for cohorts of irradiated nude mice infused with noncultured ICN1+ bone marrow–derived cells (A; 5 mice/group; P = .03 by log-rank test), nonirradiated nude mice infused with ICN1+ bone marrow–derived cells after 12 days of culture (B; 9 Arf+/+, 8 Arf−/− recipient mice, P = .002), and nonirradiated nude mice infused with cultured ICN1+ thymus-derived cells (C; 3 mice/group, P = .02). Representative immunophenotypes of T-ALLs arising in each experiment are depicted in panels to the right of the corresponding survival curves (D-F). Although all leukemias had a dominant CD4+/CD8+ population, several also had CD8 single-positive subpopulations.

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