Figure 3
Figure 3. Stability of CD147 expression. (A) CD4+ T cells, either enriched or depleted for CD25, were stimulated for 48 hours by anti-CD3/anti-CD2/anti-CD28–coated beads at a 1:2 ratio of beads to cells. Resting and activated T cells were then analyzed for their expression of CD25, FoxP3, and CD45RO versus CD147. Mean fluorescence intensities (MFI) in doubly positive cells are indicated. (B) CD4+CD25+CD147+ and CD4+CD25+CD147− T cells were FACS sorted to > 96% purity as determined by their CD147 expression and activated by CD23/CD3/CD28-coated beads for 48 hours. Expression profiles of CD25, CD147, and FoxP3 under resting and stimulating conditions were analyzed by flow cytometry and compared in histogram-overlay analysis.

Stability of CD147 expression. (A) CD4+ T cells, either enriched or depleted for CD25, were stimulated for 48 hours by anti-CD3/anti-CD2/anti-CD28–coated beads at a 1:2 ratio of beads to cells. Resting and activated T cells were then analyzed for their expression of CD25, FoxP3, and CD45RO versus CD147. Mean fluorescence intensities (MFI) in doubly positive cells are indicated. (B) CD4+CD25+CD147+ and CD4+CD25+CD147 T cells were FACS sorted to > 96% purity as determined by their CD147 expression and activated by CD23/CD3/CD28-coated beads for 48 hours. Expression profiles of CD25, CD147, and FoxP3 under resting and stimulating conditions were analyzed by flow cytometry and compared in histogram-overlay analysis.

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