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. 2007 Dec 26;76(3):1207–1213. doi: 10.1128/IAI.01134-07

FIG. 3.

FIG. 3.

MHC-I cell surface levels and CD4/CD8 T-cell ratios of LMP7pos plus MECL-1pos and LMP7neg plus MECL-1neg T-cell subsets in mixed BM-chimeric mice. Lethally irradiated LMP7−/− plus MECL-1−/− mice were reconstituted with a mixture of BM from B6.SJL (wt; CD45.1pos) and LMP7−/− plus MECL-1−/− (ko; CD45.2pos) mice and 28 days later were infected with rLM-E1. (A) Splenocytes of mixed BM-chimeric mice were stained at day 28 after BM injection with fluorochrome-conjugated anti-CD45.1, anti-CD45.2, anti-CD19, and biotin-conjugated anti-H-2Kb and SAV-APC to determine the H-2Kb expression levels on the CD45.1 and CD45.2 B-cell subsets. Mean fluorescence channels are depicted (means plus standard deviations [SD]; n = 2). (B) Relative frequencies of CD45.1pos and CD45.2pos CD4 and CD8 T cells in the spleens of mixed BM-chimeric mice were determined at day 28 after BM injection and at days 7 and 46 following Listeria infection by staining with fluorochrome-conjugated anti-CD45.1, anti-CD45.2, anti-TCRβ, anti-CD4, and anti-CD8α antibodies. CD4/CD8 T-cell ratios are depicted (means plus SD; n = 2 to 5). The data are representative of two independent experiments. (C) Relative frequencies of CD4 and CD8 T cells in the spleens of CD45.1pos wt recipients reconstituted with CD45.2pos LMP7−/− plus MECL-1−/− BM and LMP7−/− plus MECL-1−/− recipients reconstituted with wt BM (means plus SD; n = 4).