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首页> 外文期刊>Reproductive sciences >Hypoxia-Mediated Soluble Fms-Like Tyrosine Kinase 1 Increase Is Not Attenuated in Interleukin 6-Deficient Mice
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Hypoxia-Mediated Soluble Fms-Like Tyrosine Kinase 1 Increase Is Not Attenuated in Interleukin 6-Deficient Mice

机译:低氧介导的可溶性Fms样酪氨酸激酶1增加在白细胞介素6缺陷小鼠中没有减弱。

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摘要

The soluble fms-like tyrosine kinase 1 (sFlt-1), known to be increased in the serum of preeclamptic patients, is a relevant factor in causing maternal symptoms like hypertension and proteinuria. In this study, we aimed to reveal whether hypoxia is a cause of increased sFlt-1 levels and inflammation markers in vivo and whether these symptoms can be attenuated by interleukin 6 (IL-6) depletion. For this purpose, pregnant wild-type (wt) mice or IL-6(-/-) mice on embryonic day 16 were placed under either normoxic (20.9% oxygen) or hypoxic (6% oxygen) conditions for 6 hours. This led to a rise of sFlt-1 levels in maternal serum, independent of the IL-6 status of the dam. Increased maternal sFlt-1 serum levels were, however, not due to an increase in sFlt-1 messenger RNA levels in the placenta. Moreover, there was no increase in inflammatory markers in neither wt mice nor IL-6(-/-) mice. This suggests that hypoxia alone does not contribute to the induction of an inflammatory placenta. Also, the hypoxia-induced rise in sFlt-1 levels seems not to be mediated by IL-6 in vivo.
机译:已知先兆子痫患者血清中可溶性fms样酪氨酸激酶1(sFlt-1)升高,是引起诸如高血压和蛋白尿的孕妇症状的相关因素。在这项研究中,我们旨在揭示缺氧是否是体内sFlt-1水平和炎症标志物增加的原因,以及这些症状是否可以通过白介素6(IL-6)耗竭而减轻。为此,将在胚胎第16天的怀孕野生型(wt)小鼠或IL-6(-/-)小鼠置于常氧(20.9%氧气)或低氧(6%氧气)条件下6小时。这导致母体血清中sFlt-1水平升高,与大坝的IL-6状态无关。然而,母亲sFlt-1血清水平升高并不是由于胎盘中sFlt-1信使RNA水平升高。此外,wt小鼠和IL-6(-/-)小鼠的炎症标志物均未增加。这表明单独的缺氧并不有助于炎症性胎盘的诱导。同样,缺氧诱导的sFlt-1水平升高似乎不是由体内IL-6介导的。

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