(A-C) Colony-forming ability of established MLL-AF9 (A), MLL-AF9/NRAS (B) and MLL-ENL (C) leukemia. cKit⁺ leukemic cells (A and B) or Mac1⁺ cells (C) were transduced with either firefly luciferase shRNA as a control (shLuc) or Msi2 shRNA (shMsi2), sorted and plated in methylcellulose media to assess primary colony formation. Representative data from two to four independent experiments are shown. Error bars represent s.e.m. *p<0.05. (D) Survival curve of mice receiving MLL-AF9/NRAS-infected control or Msi2 null KLS cells. Data shown is from three independent transplant experiments (n=11; p=0.016). (E) Survival curve of mice receiving established MLL-AF9/NRAS cKit⁺ leukemic cells derived from wild type or Msi2 null mice. Data shown is from three independent transplant experiments (control, n=14; Msi2 null, n=15; p<0.001). (F and G) Survival curve of mice receiving MLL-AF9 cells (F) or MLL-AF9/NRAS cells (G) infected with either control shLuc or shMsi2. (F, n=10, p<0.0001; G n=9, p=0.0011). (H and I) Patient-derived AML samples were infected with either a control virus (shLacZ) or MSI2 knockdown lentivirus (shMSI2), sorted and plated in methylcellulose media to assess primary colony formation. Error bars represent s.e.m. *p<0.05.
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(A) A schematic of the strategy used for genome wide gene expression analysis of Msi2-deficient AML and bcCML. (B) Representation of concordantly and discordantly regulated genes in wild type and Msi2 null bcCML and AML leukemic cells. (C) Venn diagrams displaying the intersection of probe sets that are differentially regulated in wild type and Msi2 null bcCML and AML. (D and E) Heat maps indicating commonly dysregulated genes in both bcCML and MLL-AF9 leukemia (D) and top-ranked dysregulated oncogenic signals (E); selected genes linked to oncogenesis are shown. (F) Expression level of Tspan3 in different cell populations from mouse bone marrow were analyzed by RT-PCR. Representative data from two independent experiments is shown. (G) Expression level of Tspan3 in control and Msi2 null MLL-AF9 leukemia cells determined from microarray analysis; n=3, *p<0.05. (H) cKit⁺ leukemia cells from MLL-AF9/NRAS-driven AML were infected with either a control or Msi2 shRNA virus and Tspan3 expression was analyzed by RT-PCR; n=2, *p<0.05. (I) Wild type KLS cells were infected with either a control virus or Msi2-expressing virus, and expression levels of Tspan3 were analyzed by real-time PCR. Representative data from two independent experiments is shown. (J) Graph shows relative enrichment in TSPAN3, ACTIN and IGF2 mRNA levels by real-time PCR following RNA-immunoprecipitation with anti-Flag antibody from MV411 AML cells expressing Flag-GFP or Flag-Msi2. (K) Colony-forming ability of cKit⁺ cells from MLL-AF9/NRAS leukemia infected with either shLuc and Vector, shMsi2 and Vector, or shMsi2 and Tspan3. Representative data from two independent experiments is shown. Error bars represent s.e.m. *p<0.05.
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(A) Schematic diagram of integration site of gene trap vector used to generate Tspan3 null mice. (B) Spleen and whole bone marrow cells were isolated from wild type and Tspan3 null mice, and RT-PCR analysis was performed to determine expression of Tspan3. (C) Image of 2 month old wild type and Tspan3 null mice. (D) Total cellularity of bone marrow from 6 week old wild type and Tspan3 null mice. (E and F) Bone marrow cells from wild type or Tspan3 null mice were analyzed for hematopoietic lineage development; n=3. (G) Average donor chimerism in lethally irradiated recipients transplanted with wild type or Tspan3 null LT-HSCs (500 LT-HSCs/mouse); n=6 recipients per cohort. Data shown are from two independent experiments. Error bars represent s.e.m.
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(A) Experimental strategy to generate MLL-AF9/NRAS-driven leukemia from wild type or Tspan3 null mice. (B) Survival curve of mice receiving MLL-AF9/NRAS-infected wild type or Tspan3 null KLS cells. Data shown are from four independent experiments (wild type, n=19; Tspan3 null, n=15; p=0.0152). (C) Relative expression of Tspan3 mRNA in cKit⁺ Gr1⁻ cells isolated from MLL-AF9/NRAS and in bulk leukemia (p<0.05) (D) Survival curve of mice receiving established MLL-AF9/NRAS cKit⁺ leukemic cells derived from wild type or Tspan3 null mice. Data shown are from three independent experiments (wild type, n=15; Tspan3 null, n=16; p<0.0001). (E and F) Survival curve of mice receiving established MLL-AF9 (E) or MLL-AF9/NRAS cells (F) infected with either control shLuc or shTspan3 virus; (E, n=19, p=0.02; F, n=7 for control, n=10 for shTspan3, p=0.0011). (G) MLL-AF9/NRAS-driven leukemic cKit⁺ cells were obtained from wild type or Tspan3 null leukemic mice, plated in methylcellulose in the presence of the indicated cytokines for 7 days and colony formation assessed. (H) Relative expression of indicated genes in Msi2 null cKit⁺Sca1⁻Lin⁻ MLL-AF9 or Tspan3 null cKit⁺ MLL-AF9/NRAS leukemia as compared to their respective wild-type controls. Genes were selected from the genomic analysis of Msi2 null leukemic cells shown in ; n=3.
Error bars represent s.e.m., *p<0.05.
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(A) In vivo image of bone marrow region in mouse calvarium. MLL-AF9/NRAS-driven leukemic cells obtained from wild type or Tspan3 null leukemia were injected retro-orbitally into sublethally irradiated dsRed or CFP mice and the calvarial bone marrow analyzed 8 to 15 days afterward to assess localization within the bone marrow niche. The images shown were acquired in a single plane. Tspan3Gt/Gt images focus on central sinusoid region to show aberrant enrichment of cells. (B) Migration of wild type and Tspan3 null MLL-AF9/NRAS leukemic cells to SDF1 was measured 4 hours after exposure. Error bars represent s.e.m., *p<0.05. (C and D) Protein lysates from wild type and Tspan3 null -driven leukemia were analyzed by western blot for phosphorylated CXCR4 (C) and band intensity was quantified using Image J (D). (E) Colony-forming ability of cKit⁺ MLL-AF9/NRAS leukemia transduced with either firefly luciferase shRNA as a control (shLuc) or two independent CXCR4 shRNAs (shCXCR4). (F) Survival curve of mice transplanted with established cKit⁺ MLL-AF9/NRAS leukemic wild type or Tspan3 null cells. Mice were treated with 5mg/kg/day AMD3100 or vehicle (water) for 15 days, starting 6 days post-transplant (n=8 for each cohort, data compiled from two independent experiments), p<0.05 (G) Experimental scheme for imaging leukemia localization in vivo following CXCR4 inhibition (E) In vivo image of bone marrow region (red) showing defects in localization of MLL-AF9/NRAS- leukemia cells (green) following AMD3100 treatment. Dotted white line demarcates the boundary between central sinusoid and bone marrow regions. Images are maximum intensity projections of on average 60μm z-stacks. Scale bar represents 100μm. Error bars represent s.e.m., *p<0.05.
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(A) Expression of TSPAN3 is shown in bone marrow and peripheral blood samples from 42 chronic phase (CP, red bars), 17 accelerated phase (AP, green bars), and 31 blast crisis (BC, dark blue bars) CML patient samples. Gene expression data were obtained using the Rosetta platform; data are expressed as the log₁₀ ratio of the normalized expression of TSPAN3 in each patient sample compared to its expression in a pool of CP CML patients. (B) Analysis of gene expression data with increased Tspan3 in normal, AML-remission and AML-relapse samples. (C-G) Patient-derived bcCML (C), AML carrying MLL-translocations (D and E) and AML without MLL-translocations (F and G) were infected with either control (shlacZ) or TSPAN3 knockdown lentivirus (shTSPAN3), sorted and plated in methylcellulose media to assess colony formation. (H and I) Peripheral blood chimerism in NSG mice transplanted with primary patient AML samples following TSPAN3 knockdown. Patient-derived leukemic samples were infected with either control (shlacZ) or TSPAN3 knockdown lentivirus (shTSPAN3), transplanted into sublethally irradiated NSG recipients, and chimerism determined after 2 months. Data from two independent experiments are displayed relative to control set at 1. Error bars represent s.e.m. n=4, *p<0.05.
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