Figure 3
Figure 3. Reconstitution of DCs, numbers, and phenotype in the [B6 → B6Ly5.2] and [Ik−/− → B6 Ly5.2] chimeras. WT B6 Ly5.2 animals were lethally irradiated with 11 Gy and infused with 5 × 106 BM cells and 5 × 106 splenocytes from syngeneic Ly5.1 WT B6 or Ik−/− B6 donors. Four months later, these animals (n = 4-5 animals/group) were killed and the splenocytes were harvested and analyzed for total splenocyte count (A), frequency and number of CD11c+ DCs (B), and frequency and absolute numbers of CD8+CD11c+ DCs and CD8−CD11c+ DCs (C). The CD8+CD11c+ and CD8−CD11c+ DCs were analyzed for expression of CD80 (D), CD86 (E), CD40 (F), CD83 (G), and B7H1 (PD-L1) (I) I-Ab. *P < .05, **P < .01.

Reconstitution of DCs, numbers, and phenotype in the [B6 → B6Ly5.2] and [Ik−/− → B6 Ly5.2] chimeras. WT B6 Ly5.2 animals were lethally irradiated with 11 Gy and infused with 5 × 106 BM cells and 5 × 106 splenocytes from syngeneic Ly5.1 WT B6 or Ik−/− B6 donors. Four months later, these animals (n = 4-5 animals/group) were killed and the splenocytes were harvested and analyzed for total splenocyte count (A), frequency and number of CD11c+ DCs (B), and frequency and absolute numbers of CD8+CD11c+ DCs and CD8CD11c+ DCs (C). The CD8+CD11c+ and CD8CD11c+ DCs were analyzed for expression of CD80 (D), CD86 (E), CD40 (F), CD83 (G), and B7H1 (PD-L1) (I) I-Ab. *P < .05, **P < .01.

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