Fig. 8.
Fig. 8. The surface phenotype of thymic plasmacytoid cells. / (A) Plasmacytoid cells were released from a thymus tissue sample and light-density cells selected. The enriched preparation was immunofluorescent stained for IL-3Rα (PE) and HLA-DR (Cy5). HLA-DRlowIL-3Rαhigh plasmacytoid cells represented 1.5% to 2% of the preparation. HLA-DRhighIL-3Rαlow cells were composed of DCs and B cells. (B) By means of 4-color immunofluorescence staining, the phenotype of HLA-DRlow(Cy5)IL-3Rαhigh(Texas-Red) plasmacytoid cells was analyzed with the use of FITC and PE-labeled antibodies. This analysis is representative of 3 separate thymus samples.

The surface phenotype of thymic plasmacytoid cells.

(A) Plasmacytoid cells were released from a thymus tissue sample and light-density cells selected. The enriched preparation was immunofluorescent stained for IL-3Rα (PE) and HLA-DR (Cy5). HLA-DRlowIL-3Rαhigh plasmacytoid cells represented 1.5% to 2% of the preparation. HLA-DRhighIL-3Rαlow cells were composed of DCs and B cells. (B) By means of 4-color immunofluorescence staining, the phenotype of HLA-DRlow(Cy5)IL-3Rαhigh(Texas-Red) plasmacytoid cells was analyzed with the use of FITC and PE-labeled antibodies. This analysis is representative of 3 separate thymus samples.

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