SARS-CoV-2 colonization of maternal and fetal cells of the human placenta promotes alteration of local renin-angiotensin system.

Med (New York, N.y.) Pub Date : 2021-05-14 Epub Date: 2021-04-13 DOI:10.1016/j.medj.2021.04.009
Sonam Verma, Chetanchandra S Joshi, Rachel B Silverstein, Mai He, Ebony B Carter, Indira U Mysorekar
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引用次数: 39

Abstract

Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection appears to increase the risk of adverse pregnancy outcomes, such as pre-eclampsia in pregnant women. The mechanism(s) by which this occurs remains unclear.

Methods: We investigated the pathophysiology of SARS-CoV-2 at maternal-fetal interface in pregnant women who tested positive for the virus using RNA in situ hybridization (viral RNA), immunohistochemistry, and hematoxylin and eosin staining. To investigate whether viral infection alters the renin angiotensin system (RAS) in placenta, which controls blood pressure, we treated human trophoblasts with recombinant spike protein or a live modified virus with a vesicular stomatitis viral backbone expressing spike protein (VSV-S).

Findings: Viral colonization was highest in maternal decidua, fetal trophoblasts, Hofbauer cells, and in placentas delivered prematurely. We localized SARS-CoV-2 to cells expressing angiotensin-converting enzyme 2 (ACE2) and demonstrate that infected placentas had significantly reduced ACE2. In response to both spike protein and VSV-S, cellular ACE2 decreased although angiotensin II receptor type 1 (AT1R) increased with concomitant increase in soluble fms-like tyrosine kinase-1 (sFlt1). Viral infection decreased pro-angiogenic factors, AT2R, and placental growth factor, which competitively binds to sFlt1. Sera from infected pregnant women had elevated levels of sFlt1 and angiotensin II type 1-receptor autoantibodies prior to delivery, both signatory markers of pre-eclampsia.

Conclusions: SARS-CoV-2 colonizes ACE2-expressing maternal and fetal cells in the placenta. Infection in pregnant women correlates with alteration of placental RAS. As RAS regulates blood pressure, SARS-CoV-2 infection may thus increase adverse hemodynamic outcomes, such as pre-eclampsia in pregnant women.

Funding: NIH/NICHD grants R01 HD091218 and 3R01HD091218-04S1 (RADx-UP Supplement).

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人胎盘母体和胎儿细胞的SARS-CoV-2定植促进局部肾素-血管紧张素系统的改变。
背景:严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染似乎会增加孕妇发生不良妊娠结局的风险,如先兆子痫。这种现象发生的机制尚不清楚。方法:采用RNA原位杂交(病毒RNA)、免疫组织化学、苏木精和伊红染色等方法,对病毒检测呈阳性的孕妇在母胎界面进行SARS-CoV-2的病理生理研究。为了研究病毒感染是否会改变胎盘中控制血压的肾素血管紧张素系统(RAS),我们用重组刺突蛋白或表达刺突蛋白的水疱性口炎病毒主干修饰活病毒(VSV-S)处理人滋养细胞。结果:病毒定植在母体蜕膜、胎儿滋养细胞、霍夫鲍尔细胞和早产胎盘中最高。我们将SARS-CoV-2定位到表达血管紧张素转换酶2 (ACE2)的细胞上,并证明受感染的胎盘显著降低了ACE2。在对刺突蛋白和VSV-S的反应中,细胞ACE2降低,尽管血管紧张素II受体1型(AT1R)升高,同时可溶性膜样酪氨酸激酶1 (sFlt1)升高。病毒感染降低了与sFlt1竞争性结合的促血管生成因子、AT2R和胎盘生长因子。受感染孕妇的血清在分娩前sFlt1和血管紧张素II型1受体自身抗体水平升高,两者都是先兆子痫的标志性标志物。结论:SARS-CoV-2在胎盘中定植表达ace2的母体和胎儿细胞。孕妇感染与胎盘RAS的改变有关。由于RAS调节血压,SARS-CoV-2感染可能因此增加不利的血流动力学结果,如孕妇先兆子痫。资助:NIH/NICHD资助R01HD091218和3R01HD091218-04S1 (RADx-UP补充)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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