Figure 3.
Tip60 acetyltransferase activity is critical for HSC function. (A) The experimental scheme for in vivo repopulating assays: Tip60Δ/Δ (Tip60f/f; Vav-iCre) LSK cells at E13.5 (CD45.2+) were transduced with TIP60wt, TIP60mut (supplemental Figure 4B), and EV plasmid retrovirally, and transplanted into lethally irradiated recipient mice (CD45.1+), along with congenic WBM cells (CD45.1+CD45.2+). Transduction of plasmid DNA was verified by Sanger sequencing of the PCR-amplified genomic products. (B) Chimerism of recipient PB was monitored at different times for 16 weeks after the transplantation. Percentages of donor cells in total (all nucleated cell), myeloid (Gr1+Mac1+), B cells (CD19+B220+), and T cells (CD3+CD4+) of recipient PB are shown. Values are presented as means ± standard error of the mean. Statistical analyses were performed vs EV. *P < .05, ns; not significant.

Tip60 acetyltransferase activity is critical for HSC function. (A) The experimental scheme for in vivo repopulating assays: Tip60Δ/Δ (Tip60f/f; Vav-iCre) LSK cells at E13.5 (CD45.2+) were transduced with TIP60wt, TIP60mut (supplemental Figure 4B), and EV plasmid retrovirally, and transplanted into lethally irradiated recipient mice (CD45.1+), along with congenic WBM cells (CD45.1+CD45.2+). Transduction of plasmid DNA was verified by Sanger sequencing of the PCR-amplified genomic products. (B) Chimerism of recipient PB was monitored at different times for 16 weeks after the transplantation. Percentages of donor cells in total (all nucleated cell), myeloid (Gr1+Mac1+), B cells (CD19+B220+), and T cells (CD3+CD4+) of recipient PB are shown. Values are presented as means ± standard error of the mean. Statistical analyses were performed vs EV. *P < .05, ns; not significant.

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