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Canonical Non-Canonical and Atypical Pathways of Nuclear Factor кb Activation in Preeclampsia

机译:预坦克西亚核因子кB活化的规范非规范和非典型途径

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摘要

Although higher nuclear factor κB (NFκB) expression and activity is observed in preeclamptic placentas, its mechanism of activation is unknown. This is the first study to investigate whether the canonical, non-canonical, or atypical NFκB activation pathways may be responsible for the higher activation of NFκB observed in preeclamptic placentas. The study included 268 cases (130 preeclamptic women and 138 controls). We studied the expression of the genes coding for NFκB activators (NIK, IKKα, IKKβ, and CK2α) and inhibitors (IκBα and IκBβ) using RT-PCR in real time. The RT-PCR results were verified on the protein level using ELISA and Western blot. To determine the efficiency of the pathways, the ratios of activator(s) to one of the inhibitors (IκBα or IκBβ) were calculated for each studied pathway. The preeclamptic placentas demonstrated significantly lower IKKα and CK2α but higher IκBα and IκBβ protein levels. In addition, the calculated activator(s) to inhibitor (IκBα or IκBβ) ratios suggested that all studied pathways might be downregulated in preeclamptic placentas. Our results indicate that preeclamptic placentas may demonstrate mechanisms of NFκB activation other than the canonical, non-canonical, and atypical forms. In these mechanisms, inhibitors of NFκB may play a key role. These observations broaden the existing knowledge regarding the molecular background of preeclampsia development.
机译:虽然在前羊膜胎盘中观察到更高的核因子κB(NFκB)表达和活性,但其活化机制未知。这是研究规范,非规范或非典型NFκB活化途径是否可能负责在捕食性胎盘中观察到的NFκB的较高激活的研究。该研究包括268例(130名预克里姆氏症妇女和138个控件)。我们研究了NFκB活化剂(NIK,IKKα,IKKβ和CK2α)和抑制剂(IκBα和IκBβ)的基因的表达,实时使用RT-PCR。使用ELISA和Western印迹在蛋白质水平上验证RT-PCR结果。为了确定途径的效率,针对每个研究的途径计算活化剂与抑制剂之一的比例(IκBα或IκBβ)。初始胎儿胎盘显着降低IKKα和CK2α,但较高的IκBα和IκBβ蛋白水平。此外,计算的活化剂至抑制剂(IκBα或IκBβ)比率表明,所有研究的途径可能在素粘性胎盘中下调。我们的结果表明,除规范,非规范和非典型形式之外,牙槌胎盘可能表现出NFκB活化的机制。在这些机制中,NFκB的抑制剂可能发挥关键作用。这些观察结果扩大了有关先兆子痫发展的现有知识。

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