Figure 6.
Figure 6. Expression of SLAM molecules on immature DCs inhibits IL-12 production upon CD40 stimulation. Immature (nonactivated), monocyte-derived DCs were transiently transfected with the human SLAM cDNAby electroporation (Nucleofection; AMAXA). SLAM expression was measured 5 hours following transfection by flow cytometry. A representative of 4 independent experiments is shown (A). The filled histogram shows SLAM expression on DCs following transfection; the dashed line represents staining with an isotype control antibody. SLAM-transfected SLAM+ and SLAM– cells were separated 5 hours after transfection on a cell sorter. IL-12 (B) or IL-10 (C) present in the supernatants of CD40L-Lcell–activated, SLAM-sorted SLAM+ and SLAM– populations or vector-transfected controls were measured at 24 hours by ELISA. Error bars represent the standard deviation of triplicate cultures.

Expression of SLAM molecules on immature DCs inhibits IL-12 production upon CD40 stimulation. Immature (nonactivated), monocyte-derived DCs were transiently transfected with the human SLAM cDNAby electroporation (Nucleofection; AMAXA). SLAM expression was measured 5 hours following transfection by flow cytometry. A representative of 4 independent experiments is shown (A). The filled histogram shows SLAM expression on DCs following transfection; the dashed line represents staining with an isotype control antibody. SLAM-transfected SLAM+ and SLAM cells were separated 5 hours after transfection on a cell sorter. IL-12 (B) or IL-10 (C) present in the supernatants of CD40L-Lcell–activated, SLAM-sorted SLAM+ and SLAM populations or vector-transfected controls were measured at 24 hours by ELISA. Error bars represent the standard deviation of triplicate cultures.

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