Figure 4
Figure 4. Phenotypic evaluation of the immune-suppressive subset CD11blow/−/CD16− contained within BM-MDSCs. (A) Flow cytometric analysis of CD11blow/−/CD16− cells sorted from BM-MDSCs. The expression of putative MDSCs markers, markers of mature and immature myeloid cells, and markers associated with tolerance was evaluated relative to isotype control (black histograms). In the figure is presented 1 representative of 2 independent experiments. (B) Confocal microscopic localization of MPO and ARG1 in CD11blow/−/CD16− cells, freshly isolated neutrophils, and monocytes. Scale bars = 12 μm. (C) Localization of MPO and ARG1 in CD11blow/−/CD16−, CD11b+/CD16−, and CD11b+/CD16+ cells isolated from fresh BM samples determined by confocal microscopy. Scale bars = 20 μm.

Phenotypic evaluation of the immune-suppressive subset CD11blow/−/CD16 contained within BM-MDSCs. (A) Flow cytometric analysis of CD11blow/−/CD16 cells sorted from BM-MDSCs. The expression of putative MDSCs markers, markers of mature and immature myeloid cells, and markers associated with tolerance was evaluated relative to isotype control (black histograms). In the figure is presented 1 representative of 2 independent experiments. (B) Confocal microscopic localization of MPO and ARG1 in CD11blow/−/CD16 cells, freshly isolated neutrophils, and monocytes. Scale bars = 12 μm. (C) Localization of MPO and ARG1 in CD11blow/−/CD16, CD11b+/CD16, and CD11b+/CD16+ cells isolated from fresh BM samples determined by confocal microscopy. Scale bars = 20 μm.

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