Figure 1.
Figure 1. MSCs inhibit T-cell effector function without interfering with T-cell activation. Splenocytes from C6 mice transgenic for a Kk-restricted HY-specific T-cell receptor (TCR) (5 × 106) were stimulated for 24 hours with irradiated female syngeneic (CBA, H2k) spleen cells (5 × 106) pulsed with the cognate HY KkSmcy (TENSGKDI) peptide in the absence (A) or the presence (B) of MSCs (1 × 105). After 24 hours, CD8+ cells were analyzed for intracellular IFN-γ and for the expression of activation molecules using anti-CD25 or anti-CD69 monoclonal antibodies. For IFN-γ staining, T cells were treated with Brefeldin A for the last 4 hours of cultures. Cells were permeabilized, and the proportion of CD8+/IFN-γ+ T cells was quantified. The fluorescence-activated cell sorter (FACS) plot is representative of 1 of 6 experiments of identical design (see “Results” for mean ± SD values).

MSCs inhibit T-cell effector function without interfering with T-cell activation. Splenocytes from C6 mice transgenic for a Kk-restricted HY-specific T-cell receptor (TCR) (5 × 106) were stimulated for 24 hours with irradiated female syngeneic (CBA, H2k) spleen cells (5 × 106) pulsed with the cognate HY KkSmcy (TENSGKDI) peptide in the absence (A) or the presence (B) of MSCs (1 × 105). After 24 hours, CD8+ cells were analyzed for intracellular IFN-γ and for the expression of activation molecules using anti-CD25 or anti-CD69 monoclonal antibodies. For IFN-γ staining, T cells were treated with Brefeldin A for the last 4 hours of cultures. Cells were permeabilized, and the proportion of CD8+/IFN-γ+ T cells was quantified. The fluorescence-activated cell sorter (FACS) plot is representative of 1 of 6 experiments of identical design (see “Results” for mean ± SD values).

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