Fig. 3.
Fig. 3. Accumulation of phenotypically-immature myeloid cells in the bone marrow of IL-2−/− mice. Bone marrow cells from 6-week old wild-type (+/+) and IL-2−/− (−/−) littermates were stained with biotin-labeled Mac-1 or Gr-1 antibodies followed by SA-PE and analyzed by flow cytometry. Note the reduction in the size of the mature granulocytes (Gr-1hi) and myelomonocytic (Mac-1hi) cell populations in IL-2−/− mice. The level of staining obtained with isotype-matched control antibodies was used to determine the frequency of cells stained with Mac-1 and Gr-1 antibodies (% values shown in each histogram). The results shown are representative of eight independent experiments.

Accumulation of phenotypically-immature myeloid cells in the bone marrow of IL-2−/− mice. Bone marrow cells from 6-week old wild-type (+/+) and IL-2−/− (−/−) littermates were stained with biotin-labeled Mac-1 or Gr-1 antibodies followed by SA-PE and analyzed by flow cytometry. Note the reduction in the size of the mature granulocytes (Gr-1hi) and myelomonocytic (Mac-1hi) cell populations in IL-2−/− mice. The level of staining obtained with isotype-matched control antibodies was used to determine the frequency of cells stained with Mac-1 and Gr-1 antibodies (% values shown in each histogram). The results shown are representative of eight independent experiments.

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