Figure 3.
Figure 3. Analysis of B lymphopoiesis in Lyl-1 KO mice. (A) Quantification of B cells in total BM from wt, Lyl-1+/– and Lyl-1–/– mice. The proportion of CD19+ cells among B220+ cells is shown. (B) Quantification of pro–B (B220+ CD19–D43+ IgM–), pre–B (B220+ CD19+ CD43+ IgM–), and immature B (B220+ CD19+ CD43–IgM+) cells in BM from wt, Lyl-1+/–, and Lyl-1–/– mice. (A-B) Mean ± SEM of 3 independent experiments (*P < .05). (C) Comparison of the quantity of CLPs in the BM of wt and Lyl-1–deficient mice. BM cells were incubated with a cocktail of biotin anti-Lin, PE–anti–IL-7R, FITC–anti–Sca-1, and APC–anti–c-Kit mAb in a first step and were stained with streptavidin-PE–Cy-7 in a second step. Shown are representative flow cytometric profiles determining the frequency of CLP cells obtained (Lin–, IL7R+, sca-1+/low, c-Kit+/low).

Analysis of B lymphopoiesis in Lyl-1 KO mice. (A) Quantification of B cells in total BM from wt, Lyl-1+/– and Lyl-1–/– mice. The proportion of CD19+ cells among B220+ cells is shown. (B) Quantification of pro–B (B220+ CD19D43+ IgM), pre–B (B220+ CD19+ CD43+ IgM), and immature B (B220+ CD19+ CD43IgM+) cells in BM from wt, Lyl-1+/–, and Lyl-1–/– mice. (A-B) Mean ± SEM of 3 independent experiments (*P < .05). (C) Comparison of the quantity of CLPs in the BM of wt and Lyl-1–deficient mice. BM cells were incubated with a cocktail of biotin anti-Lin, PE–anti–IL-7R, FITC–anti–Sca-1, and APC–anti–c-Kit mAb in a first step and were stained with streptavidin-PE–Cy-7 in a second step. Shown are representative flow cytometric profiles determining the frequency of CLP cells obtained (Lin, IL7R+, sca-1+/low, c-Kit+/low).

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