Department of Life Science, Shantou University, Shantou, People's Republic of China.
Fertil Steril. 2012 May;97(5):1199-205.e1-9. doi: 10.1016/j.fertnstert.2012.02.011. Epub 2012 Feb 25.
To investigate the role of arachidonic acid (AA) in mouse endometrial stromal cells.
Experimental animal study.
University research laboratory.
ANIMAL(S): Sexually mature female CD1-strain mice.
INTERVENTION(S): Primary culture of endometrial stromal cells.
MAIN OUTCOME MEASURE(S): Western blot and real-time polymerase chain reaction for gene expression and/or phosphorylation analysis. Luciferase assay for Cox-2 promoter analysis.
RESULT(S): AA-derived prostaglandins play important roles during embryo implantation and decidualization. However, the function of AA itself in reproduction is largely unknown. In this study, exogenous AA stimulated cPLA(2α) phosphorylation and COX-2 expression, mainly through ERK1/2 in mouse endometrial stromal cells, and p38 inhibitor modestly inhibited cPLA(2α) phosphorylation induced by AA. The induction of COX-2 by AA was diminished by short interfering RNA against C/EBPβ and inhibitory C/EBPβ (LIP). C/EBPβ binding site at -872--864 of Cox-2 promoter contributes to Cox-2 promoter activation induced by C/EBPβ transfection. The expression of C/EBPβ protein induced by AA was inhibited by p38 inhibitor, and the phosphorylation of C/EBPβ induced by AA was inhibited by p38 inhibitor and ERK1/2 inhibitor. A nonmetabolized analogue of AA (ETYA) also enhanced cPLA(2α) phosphorylation and COX-2 expression. The activation of cPLA(2α)/COX-2 by AA was not inhibited by COX inhibitor indomethacin.
CONCLUSION(S): AA can induce cPLA(2α)/COX-2 pathway activation in mouse endometrial stromal cells.
探讨花生四烯酸(AA)在小鼠子宫内膜基质细胞中的作用。
实验动物研究。
大学研究实验室。
性成熟的 CD1 品系雌性小鼠。
子宫内膜基质细胞的原代培养。
Western blot 和实时聚合酶链反应进行基因表达和/或磷酸化分析;Cox-2 启动子分析的荧光素酶测定。
AA 衍生的前列腺素在胚胎着床和蜕膜化过程中发挥重要作用。然而,AA 本身在生殖中的功能在很大程度上尚不清楚。在这项研究中,外源性 AA 刺激 cPLA(2α)磷酸化和 COX-2 表达,主要通过 ERK1/2 在小鼠子宫内膜基质细胞中,p38 抑制剂轻度抑制 AA 诱导的 cPLA(2α)磷酸化。AA 诱导的 COX-2 被针对 C/EBPβ 的短干扰 RNA 和抑制性 C/EBPβ(LIP)减弱。C/EBPβ 结合位点-872 到-864 在 Cox-2 启动子上有助于 C/EBPβ 转染诱导的 Cox-2 启动子激活。AA 诱导的 C/EBPβ 蛋白表达被 p38 抑制剂抑制,AA 诱导的 C/EBPβ 磷酸化被 p38 抑制剂和 ERK1/2 抑制剂抑制。AA 的非代谢类似物(ETYA)也增强了 cPLA(2α)磷酸化和 COX-2 表达。AA 激活 cPLA(2α)/COX-2 途径不被 COX 抑制剂吲哚美辛抑制。
AA 可诱导小鼠子宫内膜基质细胞中 cPLA(2α)/COX-2 途径的激活。