(A) Survivin expression in: (1) pro- and large pre-B cells (CD43+, B220+, IgM−, IgD−), (2) small pre-B cells (CD43−, B220+, IgM−, IgD−), (3) immature B cells (CD43−, B220+, IgM+, IgD−), (4) mature recirculating cells (CD43−, B220+, IgM+, IgD+), (5) GC B cells (CD11c−, CD43−, IgD−) and (6) non GC B cells (CD11c−, CD43−, GL7−) determined by western blot. Actin was used as a loading control. One of two independent experiments is shown. (B) Survivin expression in (1) unstimulated B cells or treated with (2, 3) 10µg/mL anti-IgM (intact or F(ab’)2 fragment, (4) 10 µg/mL LPS, (5) 5 µg/mL CpG (6) 5 µg/mL anti-CD40, (7) 25 ng/mL BAFF or (8) 100ng/mL APRIL (C) Flow cytometric analysis of splenocytes from survivinL/Lmb1Cre, survivinL/+mb1Cre, and survivin+/+mb1Cre mice with indicated antibodies. (D) Number of total splenocytes and splenic B cells from survivinL/Lmb1Cre, survivinL/+mb1Cre, and survivin+/+mb1Cre mice. (E) Flow cytometric analysis of early B cell compartment in the BM of survivinL/Lmb1Cre and survivin+/+mb1Cre mice. (F) Absolute numbers of B lineage cells at each stage of maturation in the BM of survivinL/Lmb1Cre and survivin+/+mb1Cre mice. (G) Cell cycle analysis of pro- and pre- B cells from survivinL/Lmb1Cre and survivin+/+mb1Cre mice. Results are representative of 2 independent experiments.