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Inhibition of allogeneic stimulatory function of BMDCs generated over 7 days from CD38−/− mice. DCs cultured from the bone marrow of the WT and CD38−/− mice (n = 3/group, DCs in each group were combined and distributed into 3 wells independently) were used as stimulator cells and incubated with allogeneic T cells from BALB/c mice for 3 days in an MLR. T cell proliferation was detected by CCK-8 assay. The data presented one of three independent experiments (∗p < 0.05, ∗∗p < 0.01).
