Figure 4
Figure 4. Ik−/− mice exhibit increased basophils in the absence of infection. (A) Proportion of c-kit− FcεRI+ cells in indicated tissues of naive Ik+/+ and Ik−/− mice assessed by flow cytometry. Blood basophils were evaluated for the expression of FcεRI and CD200R3 after gating on c-kit− cells. Numbers denote percentage of basophils. (B) Quantification of basophil (c-kit− FcεRI+ CD200R3+) and eosinophil (c-kit− Ly6G− Siglec-F+) numbers in bone marrow of wild-type and Ik−/− mice by TruCount bead assay. P < .05 (C) Cell surface expression of basophil markers in c-kit– FcεRI+ cells from Ik−/− bone marrow determined by flow cytometry. (D) Fluorescence-activated cell sorted Ik−/− c-kit– FcεRI+ bone marrow cells were subject to quantitative RT-PCR analysis to assess expression of lineage-specific transcription factors and proteases. Data represents mean of triplicates ± standard error of the mean. (E) Fluorescence-activated cell sorted Ik−/− c-kit– FcεRI+ cells bone marrow cells were Wright-Giemsa stained (original magnification, ×100). Results shown in panels A-B are representative of 4 (blood) and 6 (bone marrow, spleen, and liver) of mice of each genotype. (C-D) Representative of 4 mice. (E) Representative of 3 mice.

Ik−/− mice exhibit increased basophils in the absence of infection. (A) Proportion of c-kit FcεRI+ cells in indicated tissues of naive Ik+/+ and Ik−/− mice assessed by flow cytometry. Blood basophils were evaluated for the expression of FcεRI and CD200R3 after gating on c-kit cells. Numbers denote percentage of basophils. (B) Quantification of basophil (c-kit FcεRI+ CD200R3+) and eosinophil (c-kit Ly6G Siglec-F+) numbers in bone marrow of wild-type and Ik−/− mice by TruCount bead assay. P < .05 (C) Cell surface expression of basophil markers in c-kit FcεRI+ cells from Ik−/− bone marrow determined by flow cytometry. (D) Fluorescence-activated cell sorted Ik−/− c-kit FcεRI+ bone marrow cells were subject to quantitative RT-PCR analysis to assess expression of lineage-specific transcription factors and proteases. Data represents mean of triplicates ± standard error of the mean. (E) Fluorescence-activated cell sorted Ik−/− c-kit FcεRI+ cells bone marrow cells were Wright-Giemsa stained (original magnification, ×100). Results shown in panels A-B are representative of 4 (blood) and 6 (bone marrow, spleen, and liver) of mice of each genotype. (C-D) Representative of 4 mice. (E) Representative of 3 mice.

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