Mcl1 partially restores normal HSC maintenance and function of Cited2-deficient HSCs
(A) Expression of Cited2, Mcl1, Pten, Gata1, Gata2, Foxo3a, and Bmi1 in LSK cells sorted from 8-week-old Cited2CTL and Cited2CKO mice (n = 4).
(B) Schematic representation of experimental mouse cohorts; Cited2CTL, Cited2CTL;Mcl1, Cited2CKO, and Cited2CKO;Mcl1.
(C) Total number of HSC, MPP1, MPP2, and MPP3/MPP4 cell populations in BM of 8- to 10-week-old mice (n = 4–6 mice per genotype).
(D) Transplantation assay: 100 HSCs were transplanted into lethally irradiated recipients together with 200,000 unfractionated CD45.1+ BM cells.
(E) Percentage of donor-derived CD45.2+ cells in PB following transplantation (n = 4 recipients per donor; n = 2–3 donors).
(F) Percentage of donor-derived CD45.2+ cells overall in the monocyte, granulocyte, B cell, and T cell compartments of PB.
(G) Percentage of donor-derived CD45.2+ cells in total BM and HSC compartments of the recipient mice.
(H) CFU assay performed with 104 BM cells from 8- to 10-week-old mice (n = 5).
(I) Total CFC counts of primary and secondary cultures (n = 5). For (A), (C), and (E)–(I), data are mean ± SEM. ∗p < 0.05, ∗∗p < 0.01.