Figure 1
Figure 1. Akt-deficient progenitors generate marrow B-lineage precursors. (A) Representative flow cytometric analysis of BM cells from chimeras established with Akt1+/+Akt2+/− (top) or Akt1−/−Akt2−/− (bottom) progenitors 12 to 14 weeks previously. The left-most plots are gated on viable donor-derived (DAPI− Ly5B6+) cells. Numbers in plots indicate the frequency of events in the indicated gate as a function of the indicated parent population. Pro-B, CD43+ B220+ CD19+ AA4+; pre-B, CD43low B220+ IgM− AA4+; immature B, CD43− B220+ IgM+ AA4+; mature B, CD43− B220+ IgM+ AA4−. (B) Absolute cell numbers for respective BM populations were calculated using the gates shown in panel A. Error bars indicate the SEM for each group; n = 5. Data are representative of 2 separate experiments. *P ≤ .01.

Akt-deficient progenitors generate marrow B-lineage precursors. (A) Representative flow cytometric analysis of BM cells from chimeras established with Akt1+/+Akt2+/− (top) or Akt1−/−Akt2−/− (bottom) progenitors 12 to 14 weeks previously. The left-most plots are gated on viable donor-derived (DAPI Ly5B6+) cells. Numbers in plots indicate the frequency of events in the indicated gate as a function of the indicated parent population. Pro-B, CD43+ B220+ CD19+ AA4+; pre-B, CD43low B220+ IgM AA4+; immature B, CD43 B220+ IgM+ AA4+; mature B, CD43 B220+ IgM+ AA4. (B) Absolute cell numbers for respective BM populations were calculated using the gates shown in panel A. Error bars indicate the SEM for each group; n = 5. Data are representative of 2 separate experiments. *P ≤ .01.

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