Figure 2
Figure 2. Effects of the human TIP110-expressing transgene on HPCs. (A) Diagram of the TIP110 transgene cassette consisting of the CMV promoter, human TIP110 cDNA (NM_014706), and bovine growth hormone poly(A) tail. (B) Bone marrow (BM) and spleen cells were harvested from TIP110TG mice for genomic DNA isolation and PCR genotyping for the TIP110 transgene. (C) Murine embryonic fibroblasts were prepared from embryos of TIP110-transgene–expressing mice and analyzed for TIP110 protein expression by Western blotting. Cells were treated with MG132 (a proteasome inhibitor) to stabilize Tip10 protein (unpublished data). *Endogenous TIP110 expression; **transgene expression including a 6× His tag. (D-E) Cells were isolated from BM and spleens of age-matched C57B/L6 control mice and TIP110TG mice and assessed for HPCs by colony assay with progenitors expressed as absolute numbers per organ (D) or progenitors were evaluated for percentage of cells in the S phase using the tritiated thymidine kill assay for determination of cycling status (E). Open bars show WT cells; closed bars, TIP110TG cells. Data for panels B and C are from 1 of at least 3 reproducible experiments. Data in panels D and E are shown as means ± SEM for 8 individually assessed mice for each group in a total of 2 independent experiments.

Effects of the human TIP110-expressing transgene on HPCs. (A) Diagram of the TIP110 transgene cassette consisting of the CMV promoter, human TIP110 cDNA (NM_014706), and bovine growth hormone poly(A) tail. (B) Bone marrow (BM) and spleen cells were harvested from TIP110TG mice for genomic DNA isolation and PCR genotyping for the TIP110 transgene. (C) Murine embryonic fibroblasts were prepared from embryos of TIP110-transgene–expressing mice and analyzed for TIP110 protein expression by Western blotting. Cells were treated with MG132 (a proteasome inhibitor) to stabilize Tip10 protein (unpublished data). *Endogenous TIP110 expression; **transgene expression including a 6× His tag. (D-E) Cells were isolated from BM and spleens of age-matched C57B/L6 control mice and TIP110TG mice and assessed for HPCs by colony assay with progenitors expressed as absolute numbers per organ (D) or progenitors were evaluated for percentage of cells in the S phase using the tritiated thymidine kill assay for determination of cycling status (E). Open bars show WT cells; closed bars, TIP110TG cells. Data for panels B and C are from 1 of at least 3 reproducible experiments. Data in panels D and E are shown as means ± SEM for 8 individually assessed mice for each group in a total of 2 independent experiments.

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