Figure 6
Figure 6. Flow cytometric analysis of Ag transfer from loaded DCs to B cells in vivo. (A-E) DCs purified from spleen and lymph nodes were analyzed for the expression of CD11c, MHCII, and CD317 (A). Conventional DC (CD11chi MHC II +) were analyzed for CD8α and CD11b expression (B). Expression of CD103 gated on cDC CD8α+, CD11b (C) and expression of CD103 gated on cDC CD11b+ (D). Uptake of QDot605-coupled F(ab)′2 anti–mouse IgG in CD11c+ cells (E). (F-G) DCs purified as in panel A were pulsed with 50 μg/mL of QDot655 (H-I) or 605 (E-G)–coupled F(ab)′2 anti–mouse IgG as in Figure 6. Three or 4 C57Bl/6 mice in each recipient group were injected subcutaneously into the hind footpads with 2.5 × 106 pulsed DCs. PLNs were collected after 24 hours. DCs (CD11c+) and B cells (CD19+) were analyzed by flow cytometry for the presence of QDot-F(ab)′2 and CD103 (G), QDot-F(ab)′2 (F,H-I). Quantifications show the total number of DCs and B cells positive for F(ab)′2 within the collected draining PLNs.

Flow cytometric analysis of Ag transfer from loaded DCs to B cells in vivo. (A-E) DCs purified from spleen and lymph nodes were analyzed for the expression of CD11c, MHCII, and CD317 (A). Conventional DC (CD11chi MHC II +) were analyzed for CD8α and CD11b expression (B). Expression of CD103 gated on cDC CD8α+, CD11b (C) and expression of CD103 gated on cDC CD11b+ (D). Uptake of QDot605-coupled F(ab)′2 anti–mouse IgG in CD11c+ cells (E). (F-G) DCs purified as in panel A were pulsed with 50 μg/mL of QDot655 (H-I) or 605 (E-G)–coupled F(ab)′2 anti–mouse IgG as in Figure 6. Three or 4 C57Bl/6 mice in each recipient group were injected subcutaneously into the hind footpads with 2.5 × 106 pulsed DCs. PLNs were collected after 24 hours. DCs (CD11c+) and B cells (CD19+) were analyzed by flow cytometry for the presence of QDot-F(ab)′2 and CD103 (G), QDot-F(ab)′2 (F,H-I). Quantifications show the total number of DCs and B cells positive for F(ab)′2 within the collected draining PLNs.

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