Abe N, Katamura K, Shintaku N, Fukui T, Kiyomasu T, Iio J, Ueno H, Tai G, Mayumi M, Furusho K
Faculty of Medicine, Kyoto University, Kyoto, 606, Japan.
Cell Immunol. 1997 Oct 10;181(1):86-92. doi: 10.1006/cimm.1997.1180.
We investigated the effects of prostaglandin E2 and IL-4 on the acquisition of cytokine-producing ability by naive CD4(+) T cells in human umbilical cord blood. The presence of PGE2 or IL-4 at primary stimulation inhibited the production of IFN-gamma at secondary stimulation, and the combination of these stimuli resulted in cooperative effects. During primary stimulation with anti-CD3, the intracellular cAMP level was elevated in PGE2-treated cells but not in IL-4-treated or control cells. The signal provided by PGE2, but not by IL-4, was inhibited with RpcAMP, indicating that it was mediated by cAMP. After differentiation into Th2-like cells, cAMP levels in PGE2- and IL-4-treated cells were not different. Our results suggest that both PGE2 and IL-4 play important roles with distinct mechanisms in inhibiting the priming of IFN-gamma production of naive CD4(+) T cells.
我们研究了前列腺素E2和白细胞介素-4对人脐带血中初始CD4(+) T细胞产生细胞因子能力获得的影响。初次刺激时PGE2或IL-4的存在抑制了再次刺激时IFN-γ的产生,并且这些刺激的组合产生了协同作用。在用抗CD3进行初次刺激期间,PGE2处理的细胞中细胞内cAMP水平升高,而IL-4处理的细胞或对照细胞中则没有。PGE2提供的信号而非IL-4提供的信号被RpcAMP抑制,表明它是由cAMP介导的。分化为Th2样细胞后,PGE2和IL-4处理的细胞中的cAMP水平没有差异。我们的结果表明,PGE2和IL-4在抑制初始CD4(+) T细胞IFN-γ产生的启动过程中均通过不同机制发挥重要作用。