Role of FL in THPO-independent maintenance of GM but not MkE progenitors. (A) Representative FACS profile showing sorting gates for THPORhi and THPOR− LMPPs cells (top panels) and purity reanalysis (bottom panels). LSK cells were gated on the 25% highest FLT3 expressing cells to define LMPPs and further based on THPOR-high and -negative subpopulations. (B) THPORhi and THPOR− LMPPs were sorted and cultured at 1 cell per well (manually plated) in Terasaki plates with indicated cytokines and clones were scored after 7 to 8 days. Data represent mean (SD) values from 2 to 3 experiments, with 120 cells being evaluated per population and experiment. (C) The preGMPs were sorted and cultured at 1 cell per well (directly deposited from the sorter) in Terasaki plates with indicated cytokines and clones were scored after 7 to 8 days. Data represent mean (SD) values from 2 experiments, with 120 cells being evaluated per population and experiment. (D) Single-cell RT-PCR analysis of transcriptional expression of Flt3, Thpor, and coexpression of Flt3 and Thpor in preGMPs. Only cells expressing Kit were included for further analysis (> 98% of cells analyzed). Data are means (SD) from 2 experiments, in which 88 cells were analyzed per experiment. (E) Representative FACS profiles in WT and Thpo−/− and Fl−/− × Thpo−/− mice, showing frequencies of preGMPs (Lin−Kit+Sca-1−CD41−CD150−FcγR−CD105low) and GMPs (Lin−Kit+Sca-1−CD41−CD150−FcγR+). Numbers represent frequencies of gated populations relative to total BM cells, and are mean values from more than 3 experiments and 10 to 13 mice per genotype. (F) Number of total BM cells, preGMPs (Lin−Kit+Sca-1−CD41−CD150−FcγR−CD105low), GMPs (Lin−Kit+Sca-1−CD41−CD150−FcγR+), MkP (Lin−Kit+Sca-1−CD41+), and CFU-Es (Lin−Kit+Sca-1−CD41−CD150−FcγR−CD105high) in WT, Thpo−/−, and Fl−/− × Thpo−/− mice. Each dot represents an individual mouse. Data are from 3 experiments. Statistical significance was tested between Thpo−/− and Fl−/− × Thpo−/− mice. ns indicates not significant; **P < .01, ***P < .001. (G) CFU-GM cultures; 10 000 unfractionated BM cells from WT and Thpo−/− and Fl−/− × Thpo−/− mice, respectively, were added to methylcellulose supplemented with FL, IL-3, GM-CSF, and G-CSF. Clones were scored after 7 to 8 days. Each dot represents data from 1 mouse (means of 2 replicates). Data are from 3 experiments. Statistical significance was tested between Thpo−/− and Fl−/− × Thpo−/− mice. ***P < 0.001.