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. 2020 Mar 26;14(4):551–560. doi: 10.1016/j.stemcr.2020.02.011

Figure 1.

Figure 1

Loss of Dnmt3a and Tet2 Enhance Self-Renewal in HSCs to Different Degrees

(A) HSC serial transplantation schematic. In descending column order—contribution of 200 ControlMx1, Dnmt3a-KOMx1 (3aKO), and Tet2-KOMx1 (T2KO) HSCs to peripheral blood, lineage chimerism, HSC frequency, and HSC number in (B) primary (CNT n = 28; 3aKO n = 24; T2KO n = 22), (C) secondary (CNT n = 27; 3aKO n = 19; T2KO n = 21), and (D) tertiary (CNT n = 33; 3aKO n = 23; T2KO n = 19) transplants. (E) Self-renewal and (F) differentiation quotients of indicated HSC genotypes after each transplant. p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.001. Mean ± SEM is shown.