Figure 5
Figure 5. DCs generated from CLPs in response to TLR9 ligation are functional. CLPs were sorted from CpG-injected mice and cultured under conditions designed to support B lymphopoiesis. Harvested cells were then evaluated after 8 days by flow cytometry. (A) B220+CD19−CD11c+CD11b− cells were further fractionated into pDC and NK-like IKDC populations by the NK1.1 marker, whereas B220−CD19−CD11c+CD11b+ cDCs were NK1.1−. (B) The 3 categories of DCs were sorted, and their competence to respond to CpG stimulation by production of cytokines was evaluated.

DCs generated from CLPs in response to TLR9 ligation are functional. CLPs were sorted from CpG-injected mice and cultured under conditions designed to support B lymphopoiesis. Harvested cells were then evaluated after 8 days by flow cytometry. (A) B220+CD19CD11c+CD11b cells were further fractionated into pDC and NK-like IKDC populations by the NK1.1 marker, whereas B220CD19CD11c+CD11b+ cDCs were NK1.1. (B) The 3 categories of DCs were sorted, and their competence to respond to CpG stimulation by production of cytokines was evaluated.

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