Degrelle Séverine A, Buchrieser Julian, Dupressoir Anne, Porrot Françoise, Loeuillet Laurence, Schwartz Olivier, Fournier Thierry
Université Paris Cité, INSERM, UMR-S1139, Pathophysiology & Pharmacotoxicology of the Human Placenta, Pre- & Post-natal Microbiota (3PHM), 75006 Paris, France.
Inovarion, 75005 Paris, France.
iScience. 2023 Jun 15;26(7):107147. doi: 10.1016/j.isci.2023.107147. eCollection 2023 Jul 21.
Interferon-induced transmembrane proteins (IFITMs) are restriction factors that block many viruses from entering cells. High levels of type I interferon (IFN) are associated with adverse pregnancy outcomes, and IFITMs have been shown to impair the formation of syncytiotrophoblast. Here, we examine whether IFITMs affect another critical step of placental development, extravillous cytotrophoblast (EVCT) invasion. We conducted experiments using / models of EVCT, mice treated with the IFN-inducer poly (I:C), and human pathological placental sections. Cells treated with IFN-β demonstrated upregulation of IFITMs and reduced invasive abilities. Transduction experiments confirmed that IFITM1 contributed to the decreased cell invasion. Similarly, migration of trophoblast giant cells, the mouse equivalent of human EVCTs, was significantly reduced in poly (I:C)-treated mice. Finally, analysis of CMV- and bacterial-infected human placentas revealed upregulated IFITM1 expression. These data demonstrate that high levels of IFITM1 impair trophoblast invasion and could explain the placental dysfunctions associated with IFN-mediated disorders.
干扰素诱导跨膜蛋白(IFITMs)是一类限制因子,可阻止多种病毒进入细胞。高水平的I型干扰素(IFN)与不良妊娠结局相关,并且已证明IFITMs会损害合体滋养层的形成。在此,我们研究IFITMs是否会影响胎盘发育的另一个关键步骤,即绒毛外细胞滋养层(EVCT)侵袭。我们使用EVCT模型、用IFN诱导剂聚肌胞苷酸(poly (I:C))处理的小鼠以及人类病理性胎盘切片进行了实验。用IFN-β处理的细胞显示出IFITMs上调且侵袭能力降低。转导实验证实IFITM1导致细胞侵袭减少。同样,在经聚肌胞苷酸(poly (I:C))处理的小鼠中,相当于人类EVCT的滋养层巨细胞的迁移也显著减少。最后,对感染巨细胞病毒(CMV)和细菌的人类胎盘的分析显示IFITM1表达上调。这些数据表明高水平的IFITM1会损害滋养层侵袭,并可能解释与IFN介导的疾病相关的胎盘功能障碍。