Figure 1
Figure 1. c-JUN is involved in p185BCR-ABL-induced transformation and leukemogenesis. Colony formation assays were performed using 1 × 106 (A) JNK1+/− and JNK1−/− (n = 8; 2-tailed t test, 49.2 ± 7.9 vs 28.9 ± 4.1 colonies/107 fetal liver cells, P = .0401) and (B) c-Junfl/fl and c-Junfl/flCD19-Cre+/− (n = 6; 2-tailed t test, 60.5 ± 6.1 vs 27.3 ± 1.9 colonies/107 fetal liver cells, P = .0004) fetal liver cells after infection with a pMSCV-p185BCR-ABL-IRES-GFP retrovirus in growth factor–free methylcellulose. (C) Transplantation of 1 × 105 c-Junfl/fl and c-JunΔ/Δ cells into Rag2−/− mice. Two independent cell lines for each cell type were injected in 9 mice (mean survival, 11 vs 16 days in mice injected with c-Junfl/fl and c-JunΔ/Δ cells, respectively, P = .0307). (D) Spleen weights of diseased recipient Rag2−/− mice were analyzed (c-Junfl/fl [n = 9] and c-JunΔ/Δ [n = 9], 2-tailed t test, P = .0169).

c-JUN is involved in p185BCR-ABL-induced transformation and leukemogenesis. Colony formation assays were performed using 1 × 106 (A) JNK1+/− and JNK1−/− (n = 8; 2-tailed t test, 49.2 ± 7.9 vs 28.9 ± 4.1 colonies/107 fetal liver cells, P = .0401) and (B) c-Junfl/fl and c-Junfl/flCD19-Cre+/− (n = 6; 2-tailed t test, 60.5 ± 6.1 vs 27.3 ± 1.9 colonies/107 fetal liver cells, P = .0004) fetal liver cells after infection with a pMSCV-p185BCR-ABL-IRES-GFP retrovirus in growth factor–free methylcellulose. (C) Transplantation of 1 × 105c-Junfl/fl and c-JunΔ/Δ cells into Rag2−/− mice. Two independent cell lines for each cell type were injected in 9 mice (mean survival, 11 vs 16 days in mice injected with c-Junfl/fl and c-JunΔ/Δ cells, respectively, P = .0307). (D) Spleen weights of diseased recipient Rag2−/− mice were analyzed (c-Junfl/fl [n = 9] and c-JunΔ/Δ [n = 9], 2-tailed t test, P = .0169).

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