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. 2020 Apr 13;24(10):5817–5831. doi: 10.1111/jcmm.15250

Figure 7.

Figure 7

MSCs suppresses CD103+ DCs‐mediated CD8 T cells proliferation and activation. A, Representative FACS analysis showing the gating strategy to identify CD8+ T cells in vitro. Spleen mononuclear cells were incubated with CFSE and cocultured with or without CD103+ DCs (sorted form TNFα‐induced DCs) or/and MSC‐CM for 2 days. Then after pregating on CD8α+ T cells, CFSE intensity and the expression of Granzyme B in CD8α+ T cells was analysed. B and C, Percentage of CD8α+ T cells in the group of CD8α+ T cells cocultured with or without CD103+ DCs (sorted form TNFα‐induced DCs) or/and MSC‐CM for 2 days. Data shown represent the mean ± SD of each group (n = 5 per group). ***P < .001 vs NC group, ###P < .001 vs DN + Saline group. D, Representative FACS analysis showing expression of Granzyme B on CD8α+ T cells in the group of CD8α+ T cells cocultured with or without CD103+ DCs (sorted form TNFα‐induced DCs) or/and MSC‐CM for 2 days. E, Flow cytometric analysis of mean fluorescence intensity of Granzyme B on CD8α+ T cells in the group of CD8α+ T cells cocultured with or without CD103+ DCs (sorted form TNFα‐induced DCs) or/and MSC‐CM for 2 days. Data shown are the mean ± SD of each group (n = 5 per group). ***P < .001 vs NC group, ###P < .001 vs DN + Saline group. F, Real‐time PCR analysis of mRNA expression of TNFα and IFNγ in freshly isolated CD8α+ T from the group of CD8α+ T cells cocultured with or without CD103+ DCs (sorted form TNFα‐induced DCs) or/and MSC‐CM for 2 days. Data shown are the mean ± SD (n = 5 per group). ***P < .001 vs NC group, ##P < .01 vs DN + Saline group