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首页> 外文期刊>Journal of Reproductive Immunology >Increased expression of NLRP3 inflammasome in placentas from pregnant women with severe preeclampsia
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Increased expression of NLRP3 inflammasome in placentas from pregnant women with severe preeclampsia

机译:孕妇中孕妇中NLRP3炎症的表达增加了严重的预先普利坦克西亚

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Highlights ? Hyperactivation of NLRP3 inflammasome was proposed in placentas from pregnant women with severe preeclampsia. ? IL-1β, TNF-α and HMGB1may be involved in the exaggerated systemic inflammation of preeclampsia. ? Placental inflammasome activation may be involved in the pathogenesis of preeclampsia. Abstract Preeclampsia is a pregnancy disorder characterized by imbalance between pro- and anti-inflammatory cytokines associated with high plasma levels of uric acid and Interleukin-1 beta (IL-1β). The inflammasome is a protein complex that mediates innate immune responses via caspase-1 activation promoting secretion of IL-1β and IL-18 in their active forms, and also release of the high-mobility group box 1 protein (HMGB1). As the placenta seems to play an important role in the pathogenesis of PE, the present study investigated the expression of genes and proteins related to the inflammasome in placentas from pregnant women with severe preeclampsia. Placental tissue was collected from 20 normotensive pregnant women and 20 preeclamptic women, and inflammasome components, NLRP3 (NOD-like receptor family, pyrin domain-containing protein 3), caspase-1, IL-1β and IL-18, as well as tumor necrosis factor-alpha (TNF-α) and HMGB1 were evaluated by immunohistochemistry, enzyme-linked immunosorbent assay (ELISA) and also quantified by reverse transcription-qPCR (RT-qPCR). Compared with normotensive pregnant women, placenta from women with PE showed a significant increase in NLRP3, caspase-1, IL-1β, TNF-α and HMGB1 mRNA. Immunohistochemical staining of NLRP3, caspase-1, IL-1β and TNF-α in placental villi, as well as the levels of caspase-1, IL-1β, TNF-α and HMGB1 in placental homogenate were significantly higher in the preeclamptic group than in the normotensive group. However, mRNA expression of IL-18 and its protein concentrations were lower in placentas from preeclamptic women. The results suggest that placentas from pregnant women with preeclampsia show higher expression of NLRP3 inflammasome, which may be involved in the exaggerated inflammatory state in preeclampsia.
机译:强调 ? NLRP3炎性炎症的孕妇在孕妇来自严重的预先普拉克西亚的孕妇。还IL-1β,TNF-α和HMGB1May参与夸张的先兆子痫炎症。还胎盘炎炎症激活可参与预坦克敏的发病机制。摘要预液柱是一种妊娠障碍,其特征在于与高血浆水平的尿酸和白细胞介素-1β(IL-1β)相关的亲属和抗炎细胞因子之间的不平衡。炎症组是一种蛋白质复合物,其通过其活性形式通过Caspase-1激活促进IL-1β和IL-18的分泌物介导先天免疫应答,以及释放高迁移率组箱1蛋白(HMGB1)。由于胎盘似乎在体育病发病机制中发挥着重要作用,本研究研究了来自孕妇的孕妇与严重的预先普拉克西亚孕妇的孕产量相关的基因和蛋白质的表达。从20名正常孕妇和20名初始母羊女性和炎症组分中收集胎盘组织,NLRP3(NOD样受体家庭,含吡啶结构域蛋白3),Caspase-1,IL-1β和IL-18以及肿瘤通过免疫组织化学,酶联免疫吸附试验(ELISA)评估坏死因子-α(TNF-α)和HMGB1,并通过逆转录QPCR(RT-QPCR)量化。与全面孕妇的孕妇相比,来自PE妇女的胎盘显示出NLRP3,Caspase-1,IL-1β,TNF-α和HMGB1 mRNA的显着增加。在胎盘绒毛中的NLRP3,Caspase-1,IL-1β和TNF-α的免疫组织化学染色以及胎盘匀浆中的Caspase-1,IL-1β,TNF-α和HMGB1的水平明显高于在正规的群体中。然而,胎儿的胎儿妇女的IL-18和其蛋白质浓度的mRNA表达较低。结果表明,孕妇具有预先普利坦斯患者的胎盘表现出较高的NLRP3炎性炎症的表达,这可能参与预坦克敏的夸张炎症状态。

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