Decreasing Id2 levels in Gfi-1−/− BMCs restores c-Kithi LK subpopulation in short-term BM reconstitution. (A) Flow cytometric analysis of donor LSK and LK c-Kithi/c-Kitlo populations 36 days after BM transplantation. LK cells were divided into c-Kithi and c-Kitlo subpopulations. Lack of donor c-Kithi LK cells in Gfi-1−/− BMCs (middle) was restored in Gfi-1−/−;Id2+/− BMCs (right). (B) Bar graph showing proportion of CMP, MEP, and GMP donor cells in c-Kithi and c-Kitlo cells, as determined by flow cytometry. Results are representative of 3 independent experiments. (C) Bar graph showing total numbers of donor LSK LT-HSCs, ST-HSCs, and MPPs in recipient BMCs. Cellularity was calculated based on total BMCs isolated from 2 femurs and 2 tibias of each recipient. These data are representative of 3 independent experiments. Data are presented as the mean ± SD. *P < .05 for Gfi-1−/− compared with Gfi-1−/−;Id2+/− ST-HSC cellularity. (D) Flow cytometric analyses show the proportion of CMPs, MEPs, and GMPs found in total LK (top), LK c-Kithi (middle), and LK c-Kitlo (bottom) of wild-type mouse BMCs.