Figure 1
Figure 1. Development and characterization of GRKO leukemia. (A-B) Leukemia development in GRKO B6 mice receiving Notch1-overexpressing Lin−Sca1+ GRKO BMCs. Shown are representative spleen and liver tissues from naive and leukemia B6 mice (A) and histology (H&E) of spleen, liver and bone marrow from a representative leukemia mouse (B). (C) B6 mice were injected with leukemia cells (ie, splenocytes from mice receiving Lin−Sca1+ GRKO BMCs), killed when moribund, and GFP+ leukemia cells in the spleen were assessed by flow cytometry. Left panel indicates that the spleen consists of predominantly GFP+ leukemia cells; right panel shows the expression of various cell surface markers on gated GFP+ leukemia cells. (D) Naive B6 mice (n = 4) were injected intravenously with 5 × 106 cryopreserved GRKO leukemia cells and killed 2-3 weeks later for assessing leukemia development. Shown are percentages (mean ± SD) of GFP+ leukemia cells (left) and of CD25+ leukemia cells (right) in the indicated tissues.

Development and characterization of GRKO leukemia. (A-B) Leukemia development in GRKO B6 mice receiving Notch1-overexpressing LinSca1+ GRKO BMCs. Shown are representative spleen and liver tissues from naive and leukemia B6 mice (A) and histology (H&E) of spleen, liver and bone marrow from a representative leukemia mouse (B). (C) B6 mice were injected with leukemia cells (ie, splenocytes from mice receiving LinSca1+ GRKO BMCs), killed when moribund, and GFP+ leukemia cells in the spleen were assessed by flow cytometry. Left panel indicates that the spleen consists of predominantly GFP+ leukemia cells; right panel shows the expression of various cell surface markers on gated GFP+ leukemia cells. (D) Naive B6 mice (n = 4) were injected intravenously with 5 × 106 cryopreserved GRKO leukemia cells and killed 2-3 weeks later for assessing leukemia development. Shown are percentages (mean ± SD) of GFP+ leukemia cells (left) and of CD25+ leukemia cells (right) in the indicated tissues.

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