Fig. 5.
Fig. 5. The expression of Thy-1 antigen and its mRNA in thymic DCs, splenic DCs, and DCs generated from Lin−c-kit+ HPCs.Ia+CD11c+CD3−CDB220−Gr-1−NK1.1−TER-119− thymic and splenic DCs were highly purified by sorting them from low-density thymocytes and splenocytes after centrifuging on 14.5% metrizamid medium. The expression of Thy-1 antigen was reanalyzed on either freshly isolated or cultured thymic and splenic DCs upon stimulation with GM-CSF + mouse TNFα for 3 days. The percentage of Thy-1+ cells is indicated in the histograms (A). Thy-1 mRNA was examined in the indicated cells using RT-PCR (B). Total RNAs were extracted from 1 × 105 cells of splenocytes, thymocytes, splenic DCs, thymic DCs, and Lin−c-kit+ HPC-derived DCs. DCs generated from Lin−c-kit+ HPCs were further sorted into Thy-1+ and Thy-1− subpopulations. The β-actin transcripts were used as control (B). Similar experiments were performed three times and representative results are shown here.

The expression of Thy-1 antigen and its mRNA in thymic DCs, splenic DCs, and DCs generated from Linc-kit+ HPCs.Ia+CD11c+CD3CDB220Gr-1NK1.1TER-119 thymic and splenic DCs were highly purified by sorting them from low-density thymocytes and splenocytes after centrifuging on 14.5% metrizamid medium. The expression of Thy-1 antigen was reanalyzed on either freshly isolated or cultured thymic and splenic DCs upon stimulation with GM-CSF + mouse TNFα for 3 days. The percentage of Thy-1+ cells is indicated in the histograms (A). Thy-1 mRNA was examined in the indicated cells using RT-PCR (B). Total RNAs were extracted from 1 × 105 cells of splenocytes, thymocytes, splenic DCs, thymic DCs, and Linc-kit+ HPC-derived DCs. DCs generated from Linc-kit+ HPCs were further sorted into Thy-1+ and Thy-1 subpopulations. The β-actin transcripts were used as control (B). Similar experiments were performed three times and representative results are shown here.

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