Figure 5
Figure 5. Msr1 deletion does not affect the function of normal HSCs. (A) Bone marrow cells from WT and Msr1−/− mice were analyzed by FACS for the percentages of total HSCs (Lin−c-Kit+Sca-1+), LT-HSCs (Lin−c-Kit+Sca-1+CD34−), ST-HSCs (Lin−c-Kit+Sca-1+CD34+Flt3−) and MPPs (Lin−c-Kit+Sca-1+CD34+Flt3+). (B) Cells from bone marrow and peripheral blood of WT and Msr1−/− mice were analyzed by FACS for the percentages of Gr-1+, B220+ and CD3E+cells. (C) 3 doses (1 × 105, 5 × 104 and 2.5 × 104) of WT or Msr1−/− bone marrow cells were injected into lethally irradiated recipient mice. Survival curves showed that there was only a minor engraftment defect of bone marrow cells in Msr1−/− mice. (D) Msr1−/− (CD45.2) and WT (CD45.1) bone marrow cells were 1:1 mixed and then transferred into recipient mice (n = 5). 12 weeks after transplantation, FACS analysis showed the percentages of WT and Msr1−/− cells in peripheral blood of recipient mice.

Msr1 deletion does not affect the function of normal HSCs. (A) Bone marrow cells from WT and Msr1−/− mice were analyzed by FACS for the percentages of total HSCs (Linc-Kit+Sca-1+), LT-HSCs (Linc-Kit+Sca-1+CD34), ST-HSCs (Linc-Kit+Sca-1+CD34+Flt3) and MPPs (Linc-Kit+Sca-1+CD34+Flt3+). (B) Cells from bone marrow and peripheral blood of WT and Msr1−/− mice were analyzed by FACS for the percentages of Gr-1+, B220+ and CD3E+cells. (C) 3 doses (1 × 105, 5 × 104 and 2.5 × 104) of WT or Msr1−/− bone marrow cells were injected into lethally irradiated recipient mice. Survival curves showed that there was only a minor engraftment defect of bone marrow cells in Msr1−/− mice. (D) Msr1−/− (CD45.2) and WT (CD45.1) bone marrow cells were 1:1 mixed and then transferred into recipient mice (n = 5). 12 weeks after transplantation, FACS analysis showed the percentages of WT and Msr1−/− cells in peripheral blood of recipient mice.

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