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. 2010 Jan 14;5(1):e8706. doi: 10.1371/journal.pone.0008706

Figure 3. Cytokine and transcription factor profile of memory CD4+CD25CD45RO+ T cells activated with IL-4+TGF-β.

Figure 3

A) Log-transformed quantities of cytokines (pg/ml) are shown. CD4+CD25CD45RO+ T cells (1.0×106/ml in 24 well plates) were activated with pbCD3/sCD28 in presence or absence of IL-4+TGF-β. Supernatants were collected at 96hrs post activation and IFNγ, IL-2, IL-5, IL-9, IL-10, IL-13, and IL-17 were quantified by ELISA. IL-4+TGF-β treated CD4+ T cells produced significantly high IL-2 and IL-9, but significantly low IFNγ, IL-13, and IL-17, as compared to CD4+CD25CD45RO+ T cells not treated with IL-4+TGF-β (n = 3). Data is expressed as the mean±SD. B) Log-transformed ratios of mRNA copies to GAPDH mRNA copies for GATA3, RORC, IL-9, and Tbet are shown. CD4+CD25CD45RO+ T cells (1.0×106/ml in 24 well plates) were activated with pbCD3/sCD28 in presence of IL-4+TGF-β. Cells were harvested and single cell sorted. IL-9 transcripts were quantified by qt-RT-PCR. 10,000 cells comprising of total cell population (TC) was also taken and the gene expression was averaged for single cell for reference. Cells positive for IL-9 transcripts were further quantitated for GATA3, RORC, and Tbet (n = 3). As IL-9 is expressed in only 10% of all CD4+ T cells activated with pbCD3/sCD28 in presence of IL-4+TGF-β, average IL-9 mRNA copies of TC are always lower than that of a single IL-9+ cell. CD4+IL-9+ T cells expressed GATA3 and RORC, but not Tbet. C) CD4+CD25CD45RO+ T cells (1.0×106/ml in 24 well plates) were activated with pbCD3/sCD28 in presence of IL-4+TGF-β. Cells were surface stained for CD4 and intracellular stained for IL-9 and FOXP3. Cells were gated for CD4 and then IL-9+ or/and FOXP3+ cells were analyzed. 25% of CD4+IL-9+ T cells were also FOXP3+. Data are representative of seven independent experiments. D) CD4+CD25CD45RO+ T cells (1.0×106/ml in 24 well plates) were activated with pbCD3/sCD28 in presence or absence of IL-4 or TGF-β or IL-4 plus TGF-β for 96hrs and analyzed by flow cytometry for FOXP3 expression. IL-4 significantly inhibited TGF-β induced FOXP3 expression (n = 3). Data is expressed as the mean±SD.