Figure 5.
Figure 5. Migratory capacity of immature and mature MoDCs and CD1c+ PBDCs. Immature MoDCs (GM-CSF plus IL-4); freshly sorted CD1c+ PBDCs, or CD1c+ PBDCs were stimulated for 8 hours (A-B) or 24 hours (C-D) with TNF-α plus IFN-α plus PGE2, with CD40L in the presence or absence of PGE2, or with intact E coli in the presence or absence of PGE2. These were then loaded into the upper transwell chambers and examined for their capacity to migrate toward either medium alone or CCL21 present in the lower transwell chambers. The y-axis shows the number of DCs migrating through the transwell membrane (8 μm) after 2 hours. Data in panels A-D are representative of 4 separate experiments. (E) Secretion of PGE2 by unstimulated or stimulated MoDCs or CD1c+ PBDCs. Data are representative of 5 separate experiments.

Migratory capacity of immature and mature MoDCs and CD1c+ PBDCs. Immature MoDCs (GM-CSF plus IL-4); freshly sorted CD1c+ PBDCs, or CD1c+ PBDCs were stimulated for 8 hours (A-B) or 24 hours (C-D) with TNF-α plus IFN-α plus PGE2, with CD40L in the presence or absence of PGE2, or with intact E coli in the presence or absence of PGE2. These were then loaded into the upper transwell chambers and examined for their capacity to migrate toward either medium alone or CCL21 present in the lower transwell chambers. The y-axis shows the number of DCs migrating through the transwell membrane (8 μm) after 2 hours. Data in panels A-D are representative of 4 separate experiments. (E) Secretion of PGE2 by unstimulated or stimulated MoDCs or CD1c+ PBDCs. Data are representative of 5 separate experiments.

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