Fig. 6.
Fig. 6. The day 6 DC precursors differentiate into cells with typical DC markers. CD11b−/dullCD11c+and CD11b+hiCD11c+ precursors were sorted from murine Lin−c-kit+ HPC cultures stimulated with GM-CSF + SCF + TNF-α for 6 days and were cultured in the presence of GMCSF + TNF-α for an additional 5 to 8 days. At days 12 to 14, the phenotype of the CD11b−/dullCD11c+ DC-like cells derived from either CD11b−/dullCD11c+ or CD11b+hiCD11c+ precursors was determined using three-color analyses as described in the legend to Fig 2.

The day 6 DC precursors differentiate into cells with typical DC markers. CD11b−/dullCD11c+and CD11b+hiCD11c+ precursors were sorted from murine Linc-kit+ HPC cultures stimulated with GM-CSF + SCF + TNF-α for 6 days and were cultured in the presence of GMCSF + TNF-α for an additional 5 to 8 days. At days 12 to 14, the phenotype of the CD11b−/dullCD11c+ DC-like cells derived from either CD11b−/dullCD11c+ or CD11b+hiCD11c+ precursors was determined using three-color analyses as described in the legend to Fig 2.

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