针对子痫前期血管紧张素II, AT1受体的激动抗体。

Ralf Dechend, Volker Homuth, Gerd Wallukat, Dominik N Müller, Manja Krause, Joachim Dudenhausen, Hermann Haller, Friedrich C Luft
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引用次数: 81

摘要

免疫机制和循环介质可能在子痫前期的发病机制中起重要作用。我们回顾了针对血管紧张素II (Ang II)受体(AT1-AA)的激动抗体及其在该疾病发病机制中的可能作用的研究结果。AT1-AA出现在子痫前期,并在分娩后6周基本消失。AT1-AA检测依赖于使用自发跳动的新生大鼠心肌细胞进行生物测定。它们的特异性已被其他方法证实,包括免疫印迹、共定位和共免疫沉淀实验。AT1-AA诱导血管细胞和滋养细胞信号传导,包括转录因子激活。该信号导致组织因子的产生和活性氧的产生,这两者都与子痫前期有关。AT1-AA在子痫前期和其他严重高血压疾病中的作用尚未得到肯定的证实。然而,我们相信这些发现是令人信服的,值得进一步研究。
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Agonistic antibodies directed at the angiotensin II, AT1 receptor in preeclampsia.

Immune mechanisms and circulating mediators may be important in the pathogenesis of preeclampsia. We review our findings on agonistic antibodies against the angiotensin II (Ang II) receptor (AT1-AA) and their possible role in the pathogenesis of this disorder. AT1-AA appear in the course of preeclampsia and are largely gone by 6 weeks after delivery. AT1-AA detection relies on a bioassay using spontaneously beating neonatal rat cardiomyocytes. Their specificity has been documented by other methods, including Western blotting, co-localization, and co-immunoprecipitation experiments. AT1-AA induce signaling in vascular cells and trophoblasts including transcription factor activation. The signaling results in tissue factor production and reactive oxygen species generation, both of which have been implicated in preeclampsia. The role of AT1-AA in preeclampsia and other severe hypertensive conditions has not yet been proved with certainty. However, we believe the findings are compelling and warrant further study.

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