Figure 2
Figure 2. High expression of CD147 correlates with high levels of FoxP3 and CD45RO and low levels of CD127 expression. (A-C) CD4+ T cells from human buffy coats were analyzed for their FoxP3 expression with respect to CD147. Total CD4 (A-B), CD4+CD25 enriched or CD4+CD25 depleted (C) T-cell fractions were analyzed by FACS using anti-CD4, anti-CD25, anti-CD147, and anti-FoxP3 under nonstimulating conditions. The ratio of CD4+CD25+CD147+ versus CD4+CD25+CD147− T cells in CD4 enriched cell fractions from 13 healthy individual blood donors is shown (B). Distribution of the obtained ratios of CD4+CD25+CD147+ versus CD4+CD25+CD147− T cells in n = 13 donors with median (line), 25-75 (box), and 2.5-97.5 (bar) percentiles shown. (D) CD147 expression in 3 subsets of CD4+ FoxP3+ T cells as defined by CD25 expression. (E) Phenotypical analysis of CD4+CD147−FoxP3+ and CD4+CD147+FoxP3+ T cells. Cell surface marker staining was determined by flow cytometry. Similar results were observed in at least 3 independent experiments for each marker, and the results of a representative experiment are shown. (F) Flow cytometric analysis using anti-CD4, anti-CD25, anti-CD147, and anti-CD127 demonstrates the negative correlation between CD147 and CD127.

High expression of CD147 correlates with high levels of FoxP3 and CD45RO and low levels of CD127 expression. (A-C) CD4+ T cells from human buffy coats were analyzed for their FoxP3 expression with respect to CD147. Total CD4 (A-B), CD4+CD25 enriched or CD4+CD25 depleted (C) T-cell fractions were analyzed by FACS using anti-CD4, anti-CD25, anti-CD147, and anti-FoxP3 under nonstimulating conditions. The ratio of CD4+CD25+CD147+ versus CD4+CD25+CD147 T cells in CD4 enriched cell fractions from 13 healthy individual blood donors is shown (B). Distribution of the obtained ratios of CD4+CD25+CD147+ versus CD4+CD25+CD147 T cells in n = 13 donors with median (line), 25-75 (box), and 2.5-97.5 (bar) percentiles shown. (D) CD147 expression in 3 subsets of CD4+ FoxP3+ T cells as defined by CD25 expression. (E) Phenotypical analysis of CD4+CD147FoxP3+ and CD4+CD147+FoxP3+ T cells. Cell surface marker staining was determined by flow cytometry. Similar results were observed in at least 3 independent experiments for each marker, and the results of a representative experiment are shown. (F) Flow cytometric analysis using anti-CD4, anti-CD25, anti-CD147, and anti-CD127 demonstrates the negative correlation between CD147 and CD127.

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