Figure 2
Figure 2. DC accumulation and spontaneous activation of T cells in perforin−/−DC-Fas−/− mice. (A) Flow cytometry of CD11chighI-Ab+ DCs and CD11clowPDCA-1+ pDCs in 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (B) Staining of I-Ab, CD80, CD86, and ICAM-1 on CD11chighCD11b+ DCs from 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (C) Flow cytometry of F4/80+CD11b+ macrophages in 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (D) CD69 staining on CD4+, CD8+, and CD19+ cells from the spleen of 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice were analyzed by flow cytometry. Splenocytes were also stained with APC–anti-CD4 or APC–anti-CD8, and PE–anti-CD44 and cychrome–anti-CD62L. The cells were analyzed by flow cytometry. CD44 and CD62L staining of CD4+ or CD8+ cells were plotted. Data are representative of 5 independent experiments.

DC accumulation and spontaneous activation of T cells in perforin−/−DC-Fas−/− mice. (A) Flow cytometry of CD11chighI-Ab+ DCs and CD11clowPDCA-1+ pDCs in 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (B) Staining of I-Ab, CD80, CD86, and ICAM-1 on CD11chighCD11b+ DCs from 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (C) Flow cytometry of F4/80+CD11b+ macrophages in 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice. (D) CD69 staining on CD4+, CD8+, and CD19+ cells from the spleen of 4-week-old WT, perforin−/−, DC-Fas−/−, and perforin−/−DC-Fas−/− mice were analyzed by flow cytometry. Splenocytes were also stained with APC–anti-CD4 or APC–anti-CD8, and PE–anti-CD44 and cychrome–anti-CD62L. The cells were analyzed by flow cytometry. CD44 and CD62L staining of CD4+ or CD8+ cells were plotted. Data are representative of 5 independent experiments.

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