Figure 4.
Figure 4. ICN1-induced T-ALL develops with delayed kinetics in Rag2-/- mice. Rag2-/- mice were reconstituted with Rag2-/- bone marrow transduced with mICN1-containing or empty retroviruses. Cell suspensions were stained for the expression of CD4 and CD8 markers, and FACS analysis was performed to determine EGFP+ percentages in peripheral blood (PB), bone marrow (BM), and thymus (THY) of Rag2-/- mice reconstituted with Rag2-/- bone marrow transduced with mICN1-containing retroviruses 2 weeks after BMT (A, top panels), 4 weeks after BMT (B, top panels), and 8 weeks after BMT (C, top panels). Percentages of EGFP+CD4+CD8+ cells from the same samples at 2, 4, and 8 weeks after BMT are also included (A-C, bottom panels). EGFP+CD4+CD8+ cells were never detected in peripheral blood and organs from Rag2-/- mice reconstituted with Rag2-/- bone marrow transduced with empty retroviruses (data not shown). Data are representative of at least 3 independent experiments.

ICN1-induced T-ALL develops with delayed kinetics in Rag2-/- mice.Rag2-/- mice were reconstituted with Rag2-/- bone marrow transduced with mICN1-containing or empty retroviruses. Cell suspensions were stained for the expression of CD4 and CD8 markers, and FACS analysis was performed to determine EGFP+ percentages in peripheral blood (PB), bone marrow (BM), and thymus (THY) of Rag2-/- mice reconstituted with Rag2-/- bone marrow transduced with mICN1-containing retroviruses 2 weeks after BMT (A, top panels), 4 weeks after BMT (B, top panels), and 8 weeks after BMT (C, top panels). Percentages of EGFP+CD4+CD8+ cells from the same samples at 2, 4, and 8 weeks after BMT are also included (A-C, bottom panels). EGFP+CD4+CD8+ cells were never detected in peripheral blood and organs from Rag2-/- mice reconstituted with Rag2-/- bone marrow transduced with empty retroviruses (data not shown). Data are representative of at least 3 independent experiments.

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