Figure 3.
Figure 3. MN1-TEL causes aggressive myeloproliferative disease when coexpressed with IL-3 in vivo. (A) Retroviral transduction of MN1-TEL+ BM cells. BM cells were harvested from 6- to 8-week-old MN1-TEL/Mx1-Cre mice 2 weeks after the last injection with pI-pC (MN1-TEL+) or phosphate-buffered saline (PBS; MN1-TEL-). Sorted Lin- cells were transduced with pSRα–IL-3–IRES–YFP (IL-3) or pSRα-IRES-YFP (vector) retroviral vectors. Transduction efficiency was examined by FCM. A representative result of MN1-TEL+ cells transduced with IL-3 virus is shown. Uninfected WT BM cells were used as a negative control. Quadrants were determined using uninfected WT cells and GFP or YFP single-positive cells. (B) Survival analysis. Retrovirus transduced cells were transplanted into lethally irradiated syngeneic recipient mice (n = 10 in each group). Survival curves were generated according to the Kaplan-Meier method using StatView version 5.0 software (SAS Institute Inc, Cary, NC).

MN1-TEL causes aggressive myeloproliferative disease when coexpressed with IL-3 in vivo. (A) Retroviral transduction of MN1-TEL+ BM cells. BM cells were harvested from 6- to 8-week-old MN1-TEL/Mx1-Cre mice 2 weeks after the last injection with pI-pC (MN1-TEL+) or phosphate-buffered saline (PBS; MN1-TEL-). Sorted Lin- cells were transduced with pSRα–IL-3–IRES–YFP (IL-3) or pSRα-IRES-YFP (vector) retroviral vectors. Transduction efficiency was examined by FCM. A representative result of MN1-TEL+ cells transduced with IL-3 virus is shown. Uninfected WT BM cells were used as a negative control. Quadrants were determined using uninfected WT cells and GFP or YFP single-positive cells. (B) Survival analysis. Retrovirus transduced cells were transplanted into lethally irradiated syngeneic recipient mice (n = 10 in each group). Survival curves were generated according to the Kaplan-Meier method using StatView version 5.0 software (SAS Institute Inc, Cary, NC).

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