Figure 2
Figure 2. Flt3 fate mapping reveals that most erythroid and megakaryocyte progenitors are derived from Flt3-expressing progenitors. (A) EYFP expression in early thymic progenitors (LIN−CD25−KIT+; bottom left) and BM B220+ B-cell progenitors (bottom right) of Flt3-Cretg/+R26REYFP/+ mice. (B-C) Representative FACS profiles of EYFP expression in myeloid progenitor subsets (B) or LSKCD150+CD48− HSCs (also gated as FLT3−; C) in the BM of Flt3-Cretg/+R26REYFP/+ mice. Numbers in histograms are mean percentages from analysis of 3-6 mice. GMP indicates GM progenitor. (D) Quantitative RT-PCR analysis of Flt3 mRNA expression in EYFP− LSKFLT3−CD150+ CD48− and EYFP+ LSKFLT3−CD150+CD48− HSCs and LSKFLT3hi LMPPs isolated from 3-week-old Flt3-Cretg/+R26REYFP/+ mice. Mean (SEM) expression relative to Hprt, 50-100 cells/ well, 2-3 wells/mouse, 4 separate mice in total. (E) Single EYFP+ LSKFLT3−CD150+CD48− HSCs and EYFP+ Lin−SCA1+KIT−CD41−FcgR−CD150−CD105+ erythroid progenitors isolated from 4-week-old Flt3-Cretg/+R26REYFP/+ mice were analyzed for Flt3 mRNA expression. Data are expressed as mean (SEM) percentage of single Kit+ cells. A total of 64 single EYFP+ HSCs were sorted in total, of which 63 cells were Kit+, and 24 single EYFP+ erythroid progenitors were sorted, of which 24 were Kit+. (F) Quantitative PCR analysis of VWF, Gfi1b, and Runx3 expression in EYFP+ LSKFLT3− CD150+CD48−, EYFP− LSKFLT3−CD150+CD48− HSCs, and LSKFLT3hi LMPPs isolated from 3-week-old Flt3-Cretg/+R26REYFP/+ mice. Mean (SEM) expression relative to Hprt, 50-100 cells/well, 2-3 wells/mouse, 4 separate mice in total. (G) Two million BM cells from Flt3-Cretg/+R26REYFP/+ CD45.2 mice were transplanted into lethally irradiated CD45.1 recipients. At 8 weeks after transplantation, donor-derived (CD45.2) LSKEYFP+ and LSKEYFP− cells were sorted for secondary transplantation. FACS profiles show representative distribution of LSKEYFP− and LSKEYFP+ cells in primary recipients and purity analysis after sorting. (H) Five thousand purified LSKEYFP− and LSKEYFP+ cells from primary recipients of Flt3-Cretg/+R26REYFP/+ CD45.2+ BM cells were transplanted in competition with 300 000 WT CD45.1 BM cells into secondary recipients. At 6 months after transplantation, BM from recipients who underwent transplantation was analyzed for contribution of CD45.2+ cells toward the B-cell and myeloid cell lineages. To the left FACS profiles from representative mice. Percentages are mean values relative to total BM cells. To the right mean (SD) contribution in a total of 4-6 recipients each of transplanted LSKEYFP+ and LSKEYFP− cells toward total (CD45.2+), B (CD19+) and myeloid (Gr1+Mac1+) lineages at 6 months after transplantation.

Flt3 fate mapping reveals that most erythroid and megakaryocyte progenitors are derived from Flt3-expressing progenitors. (A) EYFP expression in early thymic progenitors (LINCD25KIT+; bottom left) and BM B220+ B-cell progenitors (bottom right) of Flt3-Cretg/+R26REYFP/+ mice. (B-C) Representative FACS profiles of EYFP expression in myeloid progenitor subsets (B) or LSKCD150+CD48 HSCs (also gated as FLT3; C) in the BM of Flt3-Cretg/+R26REYFP/+ mice. Numbers in histograms are mean percentages from analysis of 3-6 mice. GMP indicates GM progenitor. (D) Quantitative RT-PCR analysis of Flt3 mRNA expression in EYFP LSKFLT3CD150+ CD48 and EYFP+ LSKFLT3CD150+CD48 HSCs and LSKFLT3hi LMPPs isolated from 3-week-old Flt3-Cretg/+R26REYFP/+ mice. Mean (SEM) expression relative to Hprt, 50-100 cells/ well, 2-3 wells/mouse, 4 separate mice in total. (E) Single EYFP+ LSKFLT3CD150+CD48 HSCs and EYFP+ LinSCA1+KITCD41FcgRCD150CD105+ erythroid progenitors isolated from 4-week-old Flt3-Cretg/+R26REYFP/+ mice were analyzed for Flt3 mRNA expression. Data are expressed as mean (SEM) percentage of single Kit+ cells. A total of 64 single EYFP+ HSCs were sorted in total, of which 63 cells were Kit+, and 24 single EYFP+ erythroid progenitors were sorted, of which 24 were Kit+. (F) Quantitative PCR analysis of VWF, Gfi1b, and Runx3 expression in EYFP+ LSKFLT3 CD150+CD48, EYFP LSKFLT3CD150+CD48 HSCs, and LSKFLT3hi LMPPs isolated from 3-week-old Flt3-Cretg/+R26REYFP/+ mice. Mean (SEM) expression relative to Hprt, 50-100 cells/well, 2-3 wells/mouse, 4 separate mice in total. (G) Two million BM cells from Flt3-Cretg/+R26REYFP/+ CD45.2 mice were transplanted into lethally irradiated CD45.1 recipients. At 8 weeks after transplantation, donor-derived (CD45.2) LSKEYFP+ and LSKEYFP cells were sorted for secondary transplantation. FACS profiles show representative distribution of LSKEYFP and LSKEYFP+ cells in primary recipients and purity analysis after sorting. (H) Five thousand purified LSKEYFP and LSKEYFP+ cells from primary recipients of Flt3-Cretg/+R26REYFP/+ CD45.2+ BM cells were transplanted in competition with 300 000 WT CD45.1 BM cells into secondary recipients. At 6 months after transplantation, BM from recipients who underwent transplantation was analyzed for contribution of CD45.2+ cells toward the B-cell and myeloid cell lineages. To the left FACS profiles from representative mice. Percentages are mean values relative to total BM cells. To the right mean (SD) contribution in a total of 4-6 recipients each of transplanted LSKEYFP+ and LSKEYFP cells toward total (CD45.2+), B (CD19+) and myeloid (Gr1+Mac1+) lineages at 6 months after transplantation.

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