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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Prokineticin 1 modulates IL-8 expression via the calcineurin/NFAT signaling pathway.
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Prokineticin 1 modulates IL-8 expression via the calcineurin/NFAT signaling pathway.

机译:Prokineticin 1通过钙调神经磷酸酶/ NFAT信号通路调节IL-8表达。

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摘要

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.
机译:促动素及其受体在人子宫内膜的各个细胞区室中表达,促动素1(PROK1)在整个月经周期和怀孕期间表现出动态表达模式。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植入和早期妊娠中发挥重要作用。在这里,我们证明PROK1在稳定表达prokineticin受体1的子宫内膜上皮石川细胞和人的早孕蜕膜中诱导IL-8(一种具有血管生成特性的趋化因子)的表达。我们还显示IL-8启动子活性是由PROK1诱导的,这需要AP1和NFAT图案的存在。钙调神经磷酸酶/ NFAT信号通路的作用已通过使用特定的化学抑制剂得到证实。此外,PROK1通过钙调神经磷酸酶/ NFAT途径诱导钙调神经磷酸酶1同工型4(RCAN1-4)的调节剂的表达。 RCAN1-4的过表达证明了RCAN1-4的调节作用,这导致PROK1诱导的IL-8表达受到抑制,而RCAN1-4内源性表达的减少导致PROK1诱导的IL-8产生增加。我们的发现表明,在子宫内膜细胞中,PROK1可以激活钙调神经磷酸酶/ NFAT途径来诱导IL-8表达,而这通过诱导RCAN1-4的表达而受到负调控。

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