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人源血管紧张素受体 AT1R、AT2R 和 AT4R 的表达及其在外绒毛膜滋养细胞侵袭中的作用。

Expression of AT1R, AT2R and AT4R and their roles in extravillous trophoblast invasion in the human.

机构信息

School of Clinical Sciences, University of Nottingham, City Hospital Nottingham, Nottingham NG5 1PB, United Kingdom.

出版信息

Placenta. 2010 May;31(5):448-55. doi: 10.1016/j.placenta.2010.02.014. Epub 2010 Mar 20.

Abstract

The placental renin-angiotensin system (RAS) is active from early pregnancy and may have a role in placentation. Angiotensin II (AngII) acts via binding to receptor types AT1R and AT2R. Recently smaller peptide members of the angiotensin family have been recognised as having biological relevance. Angiotensin (3-8) (AngIV) has a specific receptor (AT4R) and evokes hypertrophy, vasodilatation and vascular inflammatory response. The aim of this study was to characterise placental expression of AT1R, AT2R and AT4R, and to determine whether AngII and AngIV regulate extravillous trophoblast (EVT) invasion, apoptosis and proliferation. Placental samples were obtained from women undergoing elective surgical termination of pregnancy (TOP) at 8-10 weeks gestation (early TOP), 12-14 weeks gestation (mid TOP) or at delivery following normal pregnancy or with pre-eclampsia (PE). Immunohistochemistry and qRT-PCR were performed to determine placental mRNA and protein expression of AT1R, AT2R and AT4R at all gestational ages. EVT invasion following culture with AngII or AngIV was assessed in early placental tissue using Matrigel invasion assays. Invasion was assessed on day 6 of culture and placental explants were harvested for immunohistochemical analysis of apoptosis and proliferation. The results from qRT-PCR and immunohistochemistry showed placental AT1R expression which did not vary with gestation. The highest levels of expression of AT2R were found in early and mid TOP placentae compared to term pregnancy. Expression of AT4R was increased in term placentae, with a significant reduction in PE placentae. Moreover, culture with AngIV or AngII increased EVT invasion from placental explants, which showed increased trophoblast proliferation and reduced apoptosis. This study has characterised expression of AT4R and AT1R and AT2R in human placenta throughout normal pregnancy and in PE. Both AngIV and AngII may play an important role in normal pregnancy.

摘要

胎盘肾素-血管紧张素系统(RAS)在早孕时活跃,并可能在胎盘形成中发挥作用。血管紧张素 II(AngII)通过与受体类型 AT1R 和 AT2R 结合发挥作用。最近,血管紧张素家族的较小肽成员已被认为具有生物学相关性。血管紧张素(3-8)(AngIV)具有特定的受体(AT4R),并引起肥大、血管舒张和血管炎症反应。本研究旨在描述胎盘 AT1R、AT2R 和 AT4R 的表达,并确定 AngII 和 AngIV 是否调节绒毛外滋养层(EVT)浸润、凋亡和增殖。从因选择性终止妊娠(TOP)而接受手术的女性中获得胎盘样本,妊娠 8-10 周(早期 TOP)、12-14 周(中期 TOP)或正常妊娠或子痫前期(PE)分娩时。进行免疫组织化学和 qRT-PCR 以确定所有妊娠年龄胎盘 AT1R、AT2R 和 AT4R 的 mRNA 和蛋白表达。使用 Matrigel 侵袭测定法在早期胎盘组织中培养 AngII 或 AngIV 后评估 EVT 浸润。在培养的第 6 天评估浸润,并从胎盘组织中提取组织用于凋亡和增殖的免疫组织化学分析。qRT-PCR 和免疫组织化学的结果显示胎盘 AT1R 的表达不随妊娠而变化。与足月妊娠相比,早期和中期 TOP 胎盘 AT2R 的表达水平最高。AT4R 的表达在足月胎盘中增加,PE 胎盘中减少。此外,用 AngIV 或 AngII 培养可增加胎盘组织中 EVT 的浸润,这表明滋养层增殖增加,凋亡减少。本研究描述了 AT4R 和 AT1R 以及 AT2R 在正常妊娠和 PE 中的表达。AngIV 和 AngII 都可能在正常妊娠中发挥重要作用。

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