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Role of Ca/CaN/NFAT signaling in IL-4 expression by splenic lymphocytes exposed to phthalate (2-ethylhexyl) ester in spleen lymphocytes

机译:Ca / CaN / NFAT信号传导在脾淋巴细胞中暴露于邻苯二甲酸(2-乙基己基)酯的脾淋巴细胞IL-4表达中的作用

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The aims of present study were to investigate the effect of phthalate (2-ethylhexyl) ester (DEHP) and mono-(2-ethylhexyl) phthalate (MEHP) on Th1/Th2 balance signaling for interleukin 4 (IL-4) expression in splenic lymphocytes, and contribution of MEHP to any hypothesized changes in vitro. Primary splenic lymphocytes were exposed to DEHP/MEHP. ELISA and Western blotting were used to detect proteins. Confocal-microscopy was used to examine nuclear translocation. Nuclear factor of activated T cells (NFAT) DNA binding activity was examined by electrophoretic mobility-shift assay. DEHP significantly increased IL-4 and interferon gamma (IFN-gamma) level, and reduced Th1/Th2 ratio (reflected by IFN-gamma/IL-4) with 5 mu g/L Concanavalin A (ConA) treatment. While MEHP reduced Th1/Th2 ratio (represented by IFN-gamma/IL-6). IL-4 mRNA was significantly increased by DEHP but not by MEHP after PMA and Ion treatment. DEHP significantly inhibited NFATp protein in cytosol and nucleus. DEHP augmented nuclear translocation of NFATc in transfected EL4 cells and NFAT DNA-binding activity. DEHP-mediated enhancement of calcium-dependent phosphatase calcineurin (CaN) protein, and NFAT and IL-4 expression were abrogated by calcium antagonist verapamil and CaN inhibitor tarcolimus. Ca2+/calmodulin antagonist chlorpromazine significantly suppressed IL-4 and CaN production with no NFAT mRNA change. Our study suggests that DEHP and MEHP impact Th1/Th2 balance by modulating different cytokines. DEHP-affected IL-4 expression through Ca/CaN/NFAT signaling pathway, but no effect was discovered for MEHP.
机译:本研究的目的是研究邻苯二甲酸(2-乙基己基)酯(DEHP)和邻苯二甲酸单-(2-乙基己基)酯(MEHP)对脾脏中白介素4(IL-4)表达的Th1 / Th2平衡信号的影响。淋巴细胞,以及MEHP对任何假设的体外变化的贡献。将原代脾淋巴细胞暴露于DEHP / MEHP。 ELISA和蛋白质印迹法用于检测蛋白质。共聚焦显微镜用于检查核易位。通过电泳迁移率变动分析检查了活化的T细胞(NFAT)DNA结合活性的核因子。用5μg / L伴刀豆球蛋白A(ConA)处理后,DEHP显着提高了IL-4和干扰素(IFN-γ)的水平,并降低了Th1 / Th2比率(被IFN-γ/ IL-4反映)。而MEHP降低了Th1 / Th2比(以IFN-γ/ IL-6表示)。在PMA和离子处理后,DEHP显着提高了IL-4 mRNA的水平,而MEHP则没有。 DEHP显着抑制胞浆和细胞核中的NFATp蛋白。 DEHP增强了NFATc在转染的EL4细胞中的核易位和NFAT DNA结合活性。钙拮抗剂维拉帕米和CaN抑制剂酒石酸废除了DEHP介导的钙依赖性磷酸酶钙调磷酸酶(CaN)蛋白的增强,以及NFAT和IL-4的表达。 Ca2 + /钙调蛋白拮抗剂氯丙嗪可显着抑制IL-4和CaN的产生,而NFAT mRNA无变化。我们的研究表明,DEHP和MEHP通过调节不同的细胞因子影响Th1 / Th2平衡。 DEHP通过Ca / CaN / NFAT信号通路影响IL-4的表达,但未发现MEHP的作用。

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