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. 2019 Aug 28;34(2):630–634. doi: 10.1038/s41375-019-0551-4

Fig. 2.

Fig. 2

AE9a-expressing bone marrow cells exhibit enhanced stem cell characteristics but do not initiate leukemogenesis. a, left, AE9a-expressing cells show enhanced proliferation capacity. Proliferation potential of Lineage, cKit+, GFP+ cells from 12 weeks old AE9a mice (red dots) and Lineage, cKit+ cells isolated from Cre-negative littermate controls (Vav, white squares) in suspension culture was estimated by cell number counts taken in seven days intervals over 3 weeks. MW  ± SD, n = 2. a, right, AE9a-expressing cells show significant self-renewal capacity. Colony-forming potential of Lineage, cKit+, GFP+ cells from 12 weeks old AE9a mice (red bars) and Lineage, cKit+ cells isolated from Vav1 littermate controls (white bars) was measured by serial replating on semi-solid methylcellulose medium in seven days intervals over 5 weeks. MW ± SD (error bars) of the colony-forming units of triplicates from one representative experiment with n = 2 mice/group is shown. b, left, White blood cell counts (WBC) are not altered in 16 weeks old AE9a mice (red dots) compared to Vav littermate controls (white squares). Individual and mean values of peripheral blood (PB), bone marrow (BM) and spleen (SP) from n = 4 mice/group are shown relative to the mean of the respective Vav group. (b, right) AE9a expression in the hematopoietic compartment does not influence survival of mice. Kaplan–Meier plot illustrating that survival in AE9a mice (red line, mean survival 580 days, n = 25) is not altered compared to Vav control mice (black line, mean survival 559 days, n = 9). ns, not significant; ***p < 0.001