Figure 5.
Figure 5. B-cell–DC cocultures induce CD11c+ cell maturation and increase cell division. Splenic CD11c+ cells were purified by FACS sorting and CFSE-labeled prior cocultures with B cells. CD11c+ cells alone have been used as control in these experiments. After 72 hours cells were collected and analyzed for cell division and expression of the CD86 maturation marker. Splenic CD11c+ were analyzed for purity after FACS sorting (A). SSC indicates side scatter. CFSE dilutions are shown in panel B, where B-cell–DC cocultures are represented by solid histograms and DCs alone by dotted histograms. Confirming previous results, CD86 was expressed in the large majority of the CD11c+ cells cocultured with B cells (C, top right quadrant). As expected, DC induced B-cell maturation through BLyS (C, top left quadrant).

B-cell–DC cocultures induce CD11c+ cell maturation and increase cell division. Splenic CD11c+ cells were purified by FACS sorting and CFSE-labeled prior cocultures with B cells. CD11c+ cells alone have been used as control in these experiments. After 72 hours cells were collected and analyzed for cell division and expression of the CD86 maturation marker. Splenic CD11c+ were analyzed for purity after FACS sorting (A). SSC indicates side scatter. CFSE dilutions are shown in panel B, where B-cell–DC cocultures are represented by solid histograms and DCs alone by dotted histograms. Confirming previous results, CD86 was expressed in the large majority of the CD11c+ cells cocultured with B cells (C, top right quadrant). As expected, DC induced B-cell maturation through BLyS (C, top left quadrant).

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