ESAM-Null FL HSCs Caused an Anemic Phenotype after In Vivo Transplantation
Four hundred E14.5 FL LSK CD48- cells from WT or ESAM Homo KO mice were transplanted into lethally irradiated CD45.1 recipient mice (WT, n = 4; Homo, n = 6). Fifteen weeks after transplantation, recipient mice were sacrificed and analyzed.
(A) Schematic showing the transplantation protocol.
(B) The percentages of CD45.1– CD45.2+ donor-type chimerism in whole peripheral blood (PB, left) or bone marrow (BM, middle). Percentages of donor-type chimerism in Mac1+Gr1+ myeloid, B220+ B cell, and CD3+ T cell fractions (right).
(C) The number of LSK CD150+ CD48– HSCs, Lin− c-Kit+ Sca-1– IL-7Ra− CD4– CD8– IgM− CD34+ FCγRlow common myeloid progenitors (CMPs), LSK Flt3+ IL-7Ra− lymphoid-primed multipotent progenitors (LMPPs), and Lin− c-Kitlow Sca-1–/low Flt3+ IL-7Ra+ common lymphoid progenitors (CLPs) in BM.
(D) Peripheral blood cell counts of red blood cells (RBCs) and hemoglobin (Hb).
Data are shown as means ± SEM. Statistically significant differences are represented by asterisks: ∗p < 0.05. See also Figure S2.