Figure 6.
Figure 6. TEL-AML1 promotes development of B and myeloid cells but not T cells in vivo. Sublethally irradiated mice were reconstituted with uninfected HPCs (UN; triangles) or HPCs transduced with MSCV-EGFP (M-G; squares) or MSCV-T/A (M-T/A; circles) (n = 6 for each group). Flow cytometry was performed on peripheral blood 3 weeks after transplantation (left panels) and on splenocytes (middle panels) and bone marrow cells (right panels) from the same mice 6 weeks after transplantation. Ly5.2+Ly5.1– cells were gated and analyzed for the expression of EGFP and lineage-specific cell surface markers. Plots show the percentage of EGFP–Ly5.2+ (open symbols) and EGFP+Ly5.2+ (filled symbols) donor-derived cells that also expressed (A) B220, (B) Mac1, and (C) Thy1.2. Each symbol represents data from an individual mouse, and bars represent the means within each group.

TEL-AML1 promotes development of B and myeloid cells but not T cells in vivo. Sublethally irradiated mice were reconstituted with uninfected HPCs (UN; triangles) or HPCs transduced with MSCV-EGFP (M-G; squares) or MSCV-T/A (M-T/A; circles) (n = 6 for each group). Flow cytometry was performed on peripheral blood 3 weeks after transplantation (left panels) and on splenocytes (middle panels) and bone marrow cells (right panels) from the same mice 6 weeks after transplantation. Ly5.2+Ly5.1 cells were gated and analyzed for the expression of EGFP and lineage-specific cell surface markers. Plots show the percentage of EGFPLy5.2+ (open symbols) and EGFP+Ly5.2+ (filled symbols) donor-derived cells that also expressed (A) B220, (B) Mac1, and (C) Thy1.2. Each symbol represents data from an individual mouse, and bars represent the means within each group.

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