Figure 7
Figure 7. Differentiated IL-17–producing CD25highCD27pos Tregs are characterized by the expression of CCR6. Sorted CD25highCD27posCD45RAnegCD4pos (CD25highCD27pos) Tregs and CD25negCD27pos CD45RAnegCD4pos (CD25negCD27pos) Teffs that were stimulated with allogeneic PBMCs and rIL-2 plus rIL-15 for 8 days. (A) Cell surface analysis of the indicated receptors (top) at day 8 of culture in the CD27neg and CD27pos cell gates (indicated at the left) after stimulation of CD25highCD27pos Tregs (top 2 rows) and CD25negCD27pos Teffs (bottom 2 rows). Histograms show forward scatter (FSC; y-axis) and fluorescence intensity (x-axis); numbers indicated percentage of positive cells. (B) Dot plots show combined CCR6 and CCR4 expression of the cells as described in panel A. (C) Sorted CD25highCD27pos Tregs were cultured for 8 days with allogeneic PBMCs in the presence of the indicated recombinant cytokines (left). After restimulation with PMA plus ionomycin in the presence of Brefeldin A intracellular IL-17 expression in CCR4- (left) and CCR6- (right) expressing cells was analyzed in the CD27neg cell gate. (D) Sorted CD25highCD27pos Tregs were cultured with allogeneic PBMCs in the presence of rIL-2, rIL-15, and rIL-1β. At day 8 of the culture the cells were stained with anti–CD27-FITC plus anti–CCR6-PE mAb, and subsequently the CD27negCCR6pos (CCR6pos) and CD27negCCR6neg (CCR6neg) cell populations were sorted by high-purity flow cytometric cell sorting. IL-17 production was measured as described in panel C. Density plots show IL-17 production (x-axis) and CD3 expression (y-axis). Explanatory figures are provided in Figure S3. (E) Real-time quantitative RT-PCR of the mRNA expression of RORγt and IL-17 in sorted CD27negCCR6pos (CCR6pos) and CD27negCCR6neg (CCR6neg) cell populations. The RT-PCR data shown were normalized to human HPRT1 levels, and expression in sorted CD27negCCR6neg cells obtained after differentiation of CD25negCD27pos Teffs was set as 1.0. Data in panels A through E are representative of 3 separate experiments performed with cells obtained form different blood donors. (F) Freshly peripheral blood sorted CD25highCD27posCD45RAnegCCR6pos Tregs and CD25highCD27posCD45RAnegCCR6neg Tregs were stimulated and analyzed as described in panel C. One of 3 similar experiments is shown. (Explanatory figures are provided in Figure S3.)

Differentiated IL-17–producing CD25highCD27pos Tregs are characterized by the expression of CCR6. Sorted CD25highCD27posCD45RAnegCD4pos (CD25highCD27pos) Tregs and CD25negCD27pos CD45RAnegCD4pos (CD25negCD27pos) Teffs that were stimulated with allogeneic PBMCs and rIL-2 plus rIL-15 for 8 days. (A) Cell surface analysis of the indicated receptors (top) at day 8 of culture in the CD27neg and CD27pos cell gates (indicated at the left) after stimulation of CD25highCD27pos Tregs (top 2 rows) and CD25negCD27pos Teffs (bottom 2 rows). Histograms show forward scatter (FSC; y-axis) and fluorescence intensity (x-axis); numbers indicated percentage of positive cells. (B) Dot plots show combined CCR6 and CCR4 expression of the cells as described in panel A. (C) Sorted CD25highCD27pos Tregs were cultured for 8 days with allogeneic PBMCs in the presence of the indicated recombinant cytokines (left). After restimulation with PMA plus ionomycin in the presence of Brefeldin A intracellular IL-17 expression in CCR4- (left) and CCR6- (right) expressing cells was analyzed in the CD27neg cell gate. (D) Sorted CD25highCD27pos Tregs were cultured with allogeneic PBMCs in the presence of rIL-2, rIL-15, and rIL-1β. At day 8 of the culture the cells were stained with anti–CD27-FITC plus anti–CCR6-PE mAb, and subsequently the CD27negCCR6pos (CCR6pos) and CD27negCCR6neg (CCR6neg) cell populations were sorted by high-purity flow cytometric cell sorting. IL-17 production was measured as described in panel C. Density plots show IL-17 production (x-axis) and CD3 expression (y-axis). Explanatory figures are provided in Figure S3. (E) Real-time quantitative RT-PCR of the mRNA expression of RORγt and IL-17 in sorted CD27negCCR6pos (CCR6pos) and CD27negCCR6neg (CCR6neg) cell populations. The RT-PCR data shown were normalized to human HPRT1 levels, and expression in sorted CD27negCCR6neg cells obtained after differentiation of CD25negCD27pos Teffs was set as 1.0. Data in panels A through E are representative of 3 separate experiments performed with cells obtained form different blood donors. (F) Freshly peripheral blood sorted CD25highCD27posCD45RAnegCCR6pos Tregs and CD25highCD27posCD45RAnegCCR6neg Tregs were stimulated and analyzed as described in panel C. One of 3 similar experiments is shown. (Explanatory figures are provided in Figure S3.)

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