Figure 2
Detection of blood lymphocytes and B-cell development in the BM. (A) Top panel: B (B220+) and T (CD3+) cells detected in the peripheral blood of Rag-2−/−γc−/− mice reconstituted with Glce+/+ and Glce−/− FLHSCs at 4 weeks after transplantation; representative mice are shown. Scatter plot represents individual mice measured and the mean B-/T-cell ratios (n ≥ 10). **P < .01. Bottom panel: Expression of IdoA containing HS on the cell surface of B220+ B cells was measured. Bars represent mean ± SEM (n = 4). The dotted black line indicates background staining. **P < .01. (B) BM of Glce+/+ and Glce−/− mice was isolated and stained for B220, CD117 (c-Kit), and IgM. The dot plots show 3 distinct B220+ B-cell populations; pro-B cells (Pro, CD117+/IgM−), pre-B cells (Pre, CD117−/IgM−), and immature B cells (Imm, CD117−/IgM+). Bar diagram represents mean ± SD of each subsets as percentage of the total B-cell population (n = 4).

Detection of blood lymphocytes and B-cell development in the BM. (A) Top panel: B (B220+) and T (CD3+) cells detected in the peripheral blood of Rag-2−/−γc−/− mice reconstituted with Glce+/+ and Glce−/− FLHSCs at 4 weeks after transplantation; representative mice are shown. Scatter plot represents individual mice measured and the mean B-/T-cell ratios (n ≥ 10). **P < .01. Bottom panel: Expression of IdoA containing HS on the cell surface of B220+ B cells was measured. Bars represent mean ± SEM (n = 4). The dotted black line indicates background staining. **P < .01. (B) BM of Glce+/+ and Glce−/− mice was isolated and stained for B220, CD117 (c-Kit), and IgM. The dot plots show 3 distinct B220+ B-cell populations; pro-B cells (Pro, CD117+/IgM), pre-B cells (Pre, CD117/IgM), and immature B cells (Imm, CD117/IgM+). Bar diagram represents mean ± SD of each subsets as percentage of the total B-cell population (n = 4).

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