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. 2022 Jun 20;72(1):73–85. doi: 10.1007/s00262-022-03226-0

Figure. 5.

Figure. 5

IL-10 derived from B10 activates MDSCs through the STAT3 pathway. a MDSCs were isolated from the spleens of the two groups of tumor-bearing mice on day 28 by CD115 magnetic beads and cocultured with mouse MCs isolated by density gradient centrifugation from BAFF WT and BAFF KO mouse spleens at a ratio of 1:3 for 72 h or alone, under the stimulation of LPS (1 µg/ml). The concentration of INOS in the coculture supernatant was detected by ELISA. b The culture supernatant of BWT, MDSCs cocultured with BWT, MDSCs cocultured with B.WT in the presence of IL-10 neutralizing antibody was collected and then cocultured with MDSCs for 48 h. The STAT3 phosphorylation level of MDSCs was detected by western bolt. c Statistical analysis of the STAT3 phosphorylation level of MDSCs. d Mouse MCs isolated by density gradient centrifugation were cocultured with MDSCs at a ratio of 1:3 for 72 h with or without WP1066 or colivelin stimulation. The differentiation ratio of B10 cells was detected by flow cytometry. e Statistical analysis of B10 differentiation in vitro. f Graphical abstract of MDSCs cross-talk with B10 cells by BAFF/BAFF-R pathway to promote immunosuppression in cervical cancer. Data from at least three independent experiments were analyzed using Student’s t test and are expressed as the mean ± SD. Symbols represent statistical significance. (*p < 0.05; **p < 0.01; ***p < 0.001; ****p < 0.0001)