Fig. 3.
Fig. 3. Generation of DCs. / (A) Flow cytometric analysis on splenic cells of Balb/cRAG2−/− (H-2d) mice that received transplantations 3 months earlier of Pax5−/−H-2b/d pre-B I cells. (B) Mixed lymphocyte reaction. CD11c+CD8α+ and CD8α− cells ofPax5−/− origin (H-2b) and of host Balb/c RAG2−/− (H-2d) were sorted and γ-irradiated, and 3 × 103 of these were incubated for 5 days with 2 × 105 Balb/c or C57Bl/6 lymph node cells. γ-Irradiated spleen cells (1 × 106) of Balb/c or C57Bl/6 mice were used as controls. [3H]-thymidine incorporation was measured during the last 14 hours of incubation. Stimulators were CD11+CD8α+H-2b/d, CD11+CD8α+H-2d, CD11+CD8α−H-2b/d, CD11+CD8α−H-2d, and Balb/c H-2d splenocytes, and C57Bl/6 H-2b splenocytes.

Generation of DCs.

(A) Flow cytometric analysis on splenic cells of Balb/cRAG2−/−(H-2d) mice that received transplantations 3 months earlier of Pax5−/−H-2b/d pre-B I cells. (B) Mixed lymphocyte reaction. CD11c+CD8α+ and CD8α cells ofPax5−/−origin (H-2b) and of host Balb/c RAG2−/−(H-2d) were sorted and γ-irradiated, and 3 × 103 of these were incubated for 5 days with 2 × 105 Balb/c or C57Bl/6 lymph node cells. γ-Irradiated spleen cells (1 × 106) of Balb/c or C57Bl/6 mice were used as controls. [3H]-thymidine incorporation was measured during the last 14 hours of incubation. Stimulators were CD11+CD8α+H-2b/d, CD11+CD8α+H-2d, CD11+CD8αH-2b/d, CD11+CD8αH-2d, and Balb/c H-2d splenocytes, and C57Bl/6 H-2b splenocytes.

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