Figure 3
Figure 3. Requirement for Akt1/2 for B1 B-cell development. (A) Representative analysis of peritoneal cavity lymphocytes from chimeras established with Akt1+/+Akt2+/− (top) or Akt1−/−Akt2−/− (bottom) progenitors 12 to 14 weeks previously. The leftmost plots are gated on viable donor-derived B cells (DAPI− Ly5B6+ CD19+). Numbers in plots show the frequency of events as a function of the indicated parent gate. (B) Average frequencies for the indicated subsets were calculated using the gates shown in panel A. B2, CD19+ B220+ CD43−; B1, CD19+ B220+ CD43+; B1a, CD19+ B220+ CD43+ CD5+; B1b, CD19+ B220+ CD43+ CD5−. Error bars indicate the SEM for each group; n = 5. Data are representative of 2 separate experiments. **P ≤ .01; ***P ≤ .005.

Requirement for Akt1/2 for B1 B-cell development. (A) Representative analysis of peritoneal cavity lymphocytes from chimeras established with Akt1+/+Akt2+/− (top) or Akt1−/−Akt2−/− (bottom) progenitors 12 to 14 weeks previously. The leftmost plots are gated on viable donor-derived B cells (DAPI Ly5B6+ CD19+). Numbers in plots show the frequency of events as a function of the indicated parent gate. (B) Average frequencies for the indicated subsets were calculated using the gates shown in panel A. B2, CD19+ B220+ CD43; B1, CD19+ B220+ CD43+; B1a, CD19+ B220+ CD43+ CD5+; B1b, CD19+ B220+ CD43+ CD5. Error bars indicate the SEM for each group; n = 5. Data are representative of 2 separate experiments. **P ≤ .01; ***P ≤ .005.

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