Figure 5
Figure 5. Normal homing of menin-deficient hematopoietic progenitors. (A) Unirradiated hosts: BM from TAM-treated CD45.2+ Cre-ERTm+ Men1f/f or control Cre-ERTm− Men1f/f mice was injected into the tail vein of CD45.1+ B6-SJL recipients (2.5 × 107 cells/mouse). Three days later flow cytometry was used to analyze the homing efficiency of CD45.2+ donor LSK cells in the host bone marrow. Contour plots are representative of 3 individual recipients in each group. (B) Irradiated hosts: lethally irradiated (900 rads) B6 mice were transplanted with 3 × 107 CFSE-labeled cells from TAM-treated CD45.2+ Cre-ERTm+ Men1f/f or Cre-ERTm− Men1f/f mice. The host BM and spleen were analyzed by flow cytometry 6 hours after transfer. Graphs show the absolute number of CFSE+Lin− cells recovered from 2 hind legs (mean + SEM). Contour plots are representative of 4 individual recipients in each group. WT indicates recipients of control cells; and KO, recipients of menin-deficient cells.

Normal homing of menin-deficient hematopoietic progenitors. (A) Unirradiated hosts: BM from TAM-treated CD45.2+Cre-ERTm+Men1f/f or control Cre-ERTmMen1f/f mice was injected into the tail vein of CD45.1+ B6-SJL recipients (2.5 × 107 cells/mouse). Three days later flow cytometry was used to analyze the homing efficiency of CD45.2+ donor LSK cells in the host bone marrow. Contour plots are representative of 3 individual recipients in each group. (B) Irradiated hosts: lethally irradiated (900 rads) B6 mice were transplanted with 3 × 107 CFSE-labeled cells from TAM-treated CD45.2+Cre-ERTm+Men1f/f or Cre-ERTmMen1f/f mice. The host BM and spleen were analyzed by flow cytometry 6 hours after transfer. Graphs show the absolute number of CFSE+Lin cells recovered from 2 hind legs (mean + SEM). Contour plots are representative of 4 individual recipients in each group. WT indicates recipients of control cells; and KO, recipients of menin-deficient cells.

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