Maldonado-Pérez David, Brown Pamela, Morgan Kevin, Millar Robert P, Thompson E Aubrey, Jabbour Henry N
Human Reproductive Sciences Unit, Medical Research Council, Edinburgh EH16 4TJ, UK.
Biochim Biophys Acta. 2009 Jul;1793(7):1315-24. doi: 10.1016/j.bbamcr.2009.03.008. Epub 2009 Apr 5.
Prokineticins and their receptors are expressed in various cellular compartments in human endometrium, with prokineticin 1 (PROK1) showing a dynamic pattern of expression across the menstrual cycle and during pregnancy. Previous studies suggest that PROK1 can play an important role in implantation and early pregnancy by inducing vascular remodeling and increasing vascular permeability. Here we demonstrate that PROK1 induces the expression of IL-8, a chemokine with angiogenic properties, in endometrial epithelial Ishikawa cells stably expressing prokineticin receptor 1 and in human first trimester decidua. We also show that IL-8 promoter activity is induced by PROK1 and that this requires the presence of AP1 and NFAT motifs. The role of calcineurin/NFAT signaling pathway is confirmed by the use of specific chemical inhibitors. Additionally, PROK1 induces the expression of the regulator of calcineurin 1 isoform 4 (RCAN1-4) via the calcineurin/NFAT pathway. A modulatory role for RCAN1-4 is demonstrated by RCAN1-4 overexpression which results in the inhibition of PROK1-induced IL-8 expression whereas reduction in RCAN1-4 endogenous expression results in an increase in PROK1-induced IL-8 production. Our findings show that in endometrial cells PROK1 can activate the calcineurin/NFAT pathway to induce IL-8 expression and that this is negatively modulated by the induction of expression of RCAN1-4.
促动力蛋白及其受体在人子宫内膜的各种细胞区室中表达,其中促动力蛋白1(PROK1)在整个月经周期和怀孕期间呈现动态表达模式。先前的研究表明,PROK1可通过诱导血管重塑和增加血管通透性在着床和早期妊娠中发挥重要作用。在此,我们证明PROK1在稳定表达促动力蛋白受体1的子宫内膜上皮 Ishikawa 细胞和人早孕蜕膜中诱导具有血管生成特性的趋化因子白细胞介素8(IL-8)的表达。我们还表明,PROK1可诱导IL-8启动子活性,且这需要AP1和NFAT基序的存在。使用特异性化学抑制剂证实了钙调神经磷酸酶/NFAT信号通路的作用。此外,PROK1通过钙调神经磷酸酶/NFAT途径诱导钙调神经磷酸酶调节因子1亚型4(RCAN1-4)的表达。RCAN1-4过表达证明了其调节作用,这导致PROK1诱导的IL-8表达受到抑制,而RCAN1-4内源性表达的降低导致PROK1诱导的IL-8产生增加。我们的研究结果表明,在子宫内膜细胞中,PROK1可激活钙调神经磷酸酶/NFAT途径以诱导IL-8表达,且这受到RCAN1-4表达诱导的负调节。