Dumont Tina M F, Mouillet Jean-Francois, Bayer Avaraham, Gardner Christina L, Klimstra William B, Wolf Dana G, Yagel Simcha, Balmir Fabiola, Binstock Anna, Sanfilippo Joseph S, Coyne Carolyn B, Larkin Jacob C, Sadovsky Yoel
Magee-Womens Research Institute, Pittsburgh, PA, United States; Department of OBGYN and Reproductive Sciences, University of Pittsburgh, Pittsburgh, PA, United States.
Center for Vaccine Research, University of Pittsburgh, Pittsburgh, PA, United States; Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA, United States.
Placenta. 2017 May;53:23-29. doi: 10.1016/j.placenta.2017.03.011. Epub 2017 Mar 16.
We have previously shown that miRNAs produced from the Chromosome 19 MiRNA Cluster (C19MC), which are expressed almost exclusively in primate trophoblasts and are released into the maternal circulation, reduce viral replication in non-placental cells and can modulate migratory behavior of extravillous trophoblast. We sought to define the expression pattern of C19MC miRNA in early pregnancy and in response to viral infection in vitro and in vivo.
We prospectively followed women undergoing in vitro fertilization (IVF) and determined their blood level of C19MC miRNA using RT-qPCR. To examine the effect of viral exposure on C19MC miRNAs expression, we used three systems: (1) a transgenic mouse overexpressing the C19MC cluster and exposed to Togaviridae during pregnancy, (2) cultured primary human trophoblasts exposed to Vesicular Stomatitis Virus in vitro, and (3) amniotic fluid from women exposed to cytomegalovirus during pregnancy.
In 27 IVF pregnancies, C19MC miRNAs were detected as early as 2 weeks after implantation, and their levels increased thereafter. There was no change in C19MC miRNA expression levels in the mouse placenta in response to viral exposure. Similarly, Vesicular Stomatitis Virus infection of primary human trophoblast did not selectively increase C19MC miRNA expression. C19MC miRNA expression in the amniotic fluid was not affected by vertical transmission of cytomegalovirus.
The expression of C19MC miRNAs in maternal circulation very early in pregnancy suggests a role in the establishment of the maternal-fetal interface. The levels of C19MC miRNA are not influenced by diverse types of viral infection.
我们之前已经表明,由19号染色体微小RNA簇(C19MC)产生的微小RNA几乎只在灵长类滋养层细胞中表达,并释放到母体循环中,它们可减少非胎盘细胞中的病毒复制,并能调节绒毛外滋养层细胞的迁移行为。我们试图确定C19MC微小RNA在早孕期间以及体外和体内对病毒感染的反应中的表达模式。
我们前瞻性地跟踪接受体外受精(IVF)的女性,并使用逆转录定量聚合酶链反应(RT-qPCR)测定她们血液中C19MC微小RNA的水平。为了研究病毒暴露对C19MC微小RNA表达的影响,我们使用了三个系统:(1)在孕期过表达C19MC簇并暴露于披膜病毒科的转基因小鼠,(2)体外暴露于水疱性口炎病毒的原代人滋养层细胞培养物,以及(3)孕期暴露于巨细胞病毒的女性的羊水。
在27例IVF妊娠中,早在着床后2周就检测到了C19MC微小RNA,此后其水平升高。病毒暴露后,小鼠胎盘中C19MC微小RNA的表达水平没有变化。同样,原代人滋养层细胞感染水疱性口炎病毒并没有选择性地增加C19MC微小RNA的表达。羊水中C19MC微小RNA的表达不受巨细胞病毒垂直传播的影响。
C19MC微小RNA在妊娠早期母体循环中的表达表明其在母胎界面建立中发挥作用。C19MC微小RNA的水平不受多种病毒感染类型的影响。