Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Biol Reprod. 2021 Jul 2;105(1):244-257. doi: 10.1093/biolre/ioab068.
The obstetrical conditions placenta accreta spectrum (PAS) and placenta previa are a significant source of pregnancy-associated morbidity and mortality, yet the specific molecular and cellular underpinnings of these conditions are not known. In this study, we identified misregulated gene expression patterns in tissues from placenta previa and percreta (the most extreme form of PAS) compared with control cases. By comparing this gene set with existing placental single-cell and bulk RNA-Seq datasets, we show that the upregulated genes predominantly mark extravillous trophoblasts. We performed immunofluorescence on several candidate molecules and found that PRG2 and AQPEP protein levels are upregulated in both the fetal membranes and the placental disk in both conditions. While this increased AQPEP expression remains restricted to trophoblasts, PRG2 is mislocalized and is found throughout the fetal membranes. Using a larger patient cohort with a diverse set of gestationally aged-matched controls, we validated PRG2 as a marker for both previa and PAS and AQPEP as a marker for only previa in the fetal membranes. Our findings suggest that the extraembryonic tissues surrounding the conceptus, including both the fetal membranes and the placental disk, harbor a signature of previa and PAS that is characteristic of EVTs and that may reflect increased trophoblast invasiveness.
胎盘部位滋养细胞肿瘤谱(PAS)和前置胎盘是妊娠相关发病率和死亡率的重要来源,但这些疾病的具体分子和细胞基础尚不清楚。在这项研究中,我们与对照组相比,确定了胎盘前置和胎盘植入(PAS 的最极端形式)组织中基因表达失调的模式。通过将这个基因集与现有的胎盘单细胞和批量 RNA-Seq 数据集进行比较,我们表明上调的基因主要标记了绒毛外滋养细胞。我们对几个候选分子进行了免疫荧光染色,发现 PRG2 和 AQPEP 蛋白水平在两种情况下的胎膜和胎盘盘都上调。虽然这种增加的 AQPEP 表达仍然局限于滋养细胞,但 PRG2 被错误定位并在整个胎膜中发现。使用具有多样化妊娠年龄匹配对照组的更大患者队列,我们验证了 PRG2 是前置胎盘和 PAS 的标志物,AQPEP 是胎膜中仅前置胎盘的标志物。我们的研究结果表明,胚胎周围的胚胎外组织,包括胎膜和胎盘盘,都具有前置胎盘和 PAS 的特征,这是 EVT 的特征,可能反映了滋养细胞的侵袭性增加。