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. Author manuscript; available in PMC: 2013 Dec 30.
Published in final edited form as: Clin Cancer Res. 2010 Aug 11;16(18):10.1158/1078-0432.CCR-10-0733. doi: 10.1158/1078-0432.CCR-10-0733

Fig. 5.

Fig. 5

Docetaxel differentiates MDSC into M1-like phenotype in vitro and selectively inhibits M2-like phenotype of MDSCs. A, MACS column–purified MDSCs were assayed by flow cytometry, confirmed to be >90% Gr-1+CD11b+ cells, and further used for in vitro assays. MDSCs were cultured in the presence or absence of docetaxel at 11 nmol/L for 24 h followed by analysis for M1 (CCR7) and M2 (MR) markers. A, flow cytometric analysis of the percentage of CCR7- and MR-expressing MDSCs before and after docetaxel culture. B, flow cytometric analysis of Annexin V+ MDSCs before and after docetaxel culture. C and D, percentage of Annexin V+ and Annexin V cells in CCR7+ or MR+ MDSCs. Docetaxel induced apoptosis on MDSCs, and the cells that were differentiated into M1-like phenotype were negative for Annexin V but positive for CCR7. E, cytokine analysis of supernatants of MDSCs cultured in the presence or absence of docetaxel for 24 h. Docetaxel-treated MDSCs enhance IL-12 and suppress IL-10 production.