Mice with FLT3wt/ITD mutation display multiple lineage disturbances in the BM
Immunophenotype . | Wild-type . | FLT3wt/ITD . |
---|---|---|
Immature population | ||
Lin−/low | 10.0 ± 3.6 | 36.7 ± 19.7* |
Sca-1+ | 1.9 ± 0.7 | 2.6 ± 1.4 |
c-KIT+ | 7.3 ± 4.2 | 15.6 ± 6.1* |
Myeloid lineage | ||
Mac-1+ | 30.9 ± 6.2 | 57.6 ± 14.9* |
Gr-1+ | 31.0 ± 7.6 | 62.2 ± 14.4* |
Ter119+ | 42.0 ± 9.6 | 12.4 ± 7.4* |
CD41a+ | 2.6 ± 1.4 | 1.7 ± 0.7 |
B-lymphoid lineage | ||
B220+ | 16.7 ± 5.2 | 5.6 ± 3.0* |
B220+/CD43+ | 3.3 ± 3.2 | 3.1 ± 1.8 |
B220+/CD43−/IgM− | 6.0 ± 1.8 | 1.3 ± 0.7* |
B220+/CD43−/IgM+ | 10.8 ± 4.0 | 4.4 ± 2.5* |
Dendritic cells, CD11c+ | 4.8 ± 3.6 | 14.0 ± 10.5† |
NK cells, NK1.1+ | 0.6 ± 0.6 | 0.7 ± 0.5 |
T-lymphoid lineage | ||
CD3+ | 1.8 ± 0.7 | 2.3 ± 0.6 |
CD4+ | 1.8 ± 0.6 | 1.9 ± 0.9 |
CD8a+ | 1.4 ± 0.9 | 1.6 ± 0.8 |
Immunophenotype . | Wild-type . | FLT3wt/ITD . |
---|---|---|
Immature population | ||
Lin−/low | 10.0 ± 3.6 | 36.7 ± 19.7* |
Sca-1+ | 1.9 ± 0.7 | 2.6 ± 1.4 |
c-KIT+ | 7.3 ± 4.2 | 15.6 ± 6.1* |
Myeloid lineage | ||
Mac-1+ | 30.9 ± 6.2 | 57.6 ± 14.9* |
Gr-1+ | 31.0 ± 7.6 | 62.2 ± 14.4* |
Ter119+ | 42.0 ± 9.6 | 12.4 ± 7.4* |
CD41a+ | 2.6 ± 1.4 | 1.7 ± 0.7 |
B-lymphoid lineage | ||
B220+ | 16.7 ± 5.2 | 5.6 ± 3.0* |
B220+/CD43+ | 3.3 ± 3.2 | 3.1 ± 1.8 |
B220+/CD43−/IgM− | 6.0 ± 1.8 | 1.3 ± 0.7* |
B220+/CD43−/IgM+ | 10.8 ± 4.0 | 4.4 ± 2.5* |
Dendritic cells, CD11c+ | 4.8 ± 3.6 | 14.0 ± 10.5† |
NK cells, NK1.1+ | 0.6 ± 0.6 | 0.7 ± 0.5 |
T-lymphoid lineage | ||
CD3+ | 1.8 ± 0.7 | 2.3 ± 0.6 |
CD4+ | 1.8 ± 0.6 | 1.9 ± 0.9 |
CD8a+ | 1.4 ± 0.9 | 1.6 ± 0.8 |
Cells obtained from 12-month-old wild-type and FLT3wt/ITD mice were stained with the indicated antibodies and analyzed by flow cytometry. Cell acquisition was performed on a 2-laser FACSCalibur using CellQuest software. Statistical analysis was performed based on results from 12 mice in each group. The mean percentage value plus or minus the SD of each indicated population in the total BM is shown.
P < .001.
P < .05.