Figure 1
Figure 1. RORγt+ iNKT cells respond weakly to IL-15 but are highly sensitive to TGFβ. Flow cytometry analysis to compare IL-15Rβ (CD122) and TGFβRII surface expression, and intracellular phospho-STAT5 (p-STAT5) and phospho-SMAD2/3 (p-SMAD2/3) levels in RORγt+ iNKT, RORγt− iNKT, and non-iNKT cells in the thymus of 6- to 8-week-old C57BL/6 WT mice. Dashed lines represent staining of the secondary antibody without the primary antibody. For p-STAT5 staining, cells were incubated with IL-15. Invariant NKT cells were identified by excluding B220+ and CD8+ cells and gating on CD1d tetramer+ TCRβ+ cells. Data are representative of at least 3 experiments with 1 to 2 individual mice per experiment.

RORγt+ iNKT cells respond weakly to IL-15 but are highly sensitive to TGFβ. Flow cytometry analysis to compare IL-15Rβ (CD122) and TGFβRII surface expression, and intracellular phospho-STAT5 (p-STAT5) and phospho-SMAD2/3 (p-SMAD2/3) levels in RORγt+ iNKT, RORγt iNKT, and non-iNKT cells in the thymus of 6- to 8-week-old C57BL/6 WT mice. Dashed lines represent staining of the secondary antibody without the primary antibody. For p-STAT5 staining, cells were incubated with IL-15. Invariant NKT cells were identified by excluding B220+ and CD8+ cells and gating on CD1d tetramer+ TCRβ+ cells. Data are representative of at least 3 experiments with 1 to 2 individual mice per experiment.

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