Figure 1
Figure 1. Type I IFN production and viral replication in MHV-infected splenic cDCs and pDCs. (A) Flow cytometric analysis of splenic cDCs (CD11c+PDCA-1−) and (B) splenic pDCs CD11clow B220+ PDCA-1− before FACS sorting. Gates for sorting are indicated. (C) Primary FACS-purified murine splenic cDCs or pDCs were infected with MHV at a multiplicity of infection (moi) of 1. IFN-α secretion to culture supernatants was determined by ELISA at the indicated time points. (D) Virus titers in culture supernatants were determined by plaque assay. (C-D) Data represent mean values ± SD pooled from 2 experiments. Statistical analysis was performed using Student t test (*P < .05; **P < .01).

Type I IFN production and viral replication in MHV-infected splenic cDCs and pDCs. (A) Flow cytometric analysis of splenic cDCs (CD11c+PDCA-1) and (B) splenic pDCs CD11clow B220+ PDCA-1 before FACS sorting. Gates for sorting are indicated. (C) Primary FACS-purified murine splenic cDCs or pDCs were infected with MHV at a multiplicity of infection (moi) of 1. IFN-α secretion to culture supernatants was determined by ELISA at the indicated time points. (D) Virus titers in culture supernatants were determined by plaque assay. (C-D) Data represent mean values ± SD pooled from 2 experiments. Statistical analysis was performed using Student t test (*P < .05; **P < .01).

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