Suppr超能文献

PRG2 和 AQPEP 在前置胎盘和胎盘植入的胎膜中表达异常†。

PRG2 and AQPEP are misexpressed in fetal membranes in placenta previa and percreta†.

机构信息

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.

出版信息

Biol Reprod. 2021 Jul 2;105(1):244-257. doi: 10.1093/biolre/ioab068.

Abstract

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.

摘要

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。

相似文献

1
PRG2 and AQPEP are misexpressed in fetal membranes in placenta previa and percreta†.
Biol Reprod. 2021 Jul 2;105(1):244-257. doi: 10.1093/biolre/ioab068.
3
Expression of β-catenin in human trophoblast and its role in placenta accreta and placenta previa.
J Int Med Res. 2019 Jan;47(1):206-214. doi: 10.1177/0300060518799265. Epub 2018 Nov 22.
4
Impact of placenta previa with placenta accreta spectrum disorder on fetal growth.
Ultrasound Obstet Gynecol. 2019 Nov;54(5):643-649. doi: 10.1002/uog.20244.
5
Shedding of Syncytiotrophoblast-Derived Extracellular Vesicles Is Increased in Placenta Previa and Accreta Spectrum.
Reprod Sci. 2024 Jul;31(7):2043-2048. doi: 10.1007/s43032-024-01491-1. Epub 2024 Mar 7.
8
Expression of sirtuin 2 and 7 in placenta accreta spectrum.
Rev Assoc Med Bras (1992). 2023 Aug 14;69(8):e20230360. doi: 10.1590/1806-9282.20230360. eCollection 2023.
10
Decreased placental and maternal serum TRAIL-R2 levels are associated with placenta accreta.
Placenta. 2016 Mar;39:1-6. doi: 10.1016/j.placenta.2016.01.004. Epub 2016 Jan 6.

引用本文的文献

1
Placenta: an old organ with new functions.
Front Immunol. 2024 Apr 19;15:1385762. doi: 10.3389/fimmu.2024.1385762. eCollection 2024.
2
Structural insights into the covalent regulation of PAPP-A activity by proMBP and STC2.
Cell Discov. 2022 Dec 22;8(1):137. doi: 10.1038/s41421-022-00502-2.

本文引用的文献

2
Proteomic patterns associated with response to breast cancer neoadjuvant treatment.
Mol Syst Biol. 2020 Sep;16(9):e9443. doi: 10.15252/msb.20209443.
3
Long non-coding RNA BCAR4 promotes liver cancer progression by regulating proliferation, migration and invasion.
Oncol Lett. 2020 Sep;20(3):2779-2787. doi: 10.3892/ol.2020.11826. Epub 2020 Jul 8.
4
SOX18 promotes gastric cancer metastasis through transactivating MCAM and CCL7.
Oncogene. 2020 Aug;39(33):5536-5552. doi: 10.1038/s41388-020-1378-1. Epub 2020 Jul 2.
5
Quiescin Sulfhydryl Oxidase 1 Regulates the Proliferation, Migration and Invasion of Human Glioblastoma Cells via PI3K/Akt Pathway.
Onco Targets Ther. 2020 Jun 17;13:5721-5729. doi: 10.2147/OTT.S255941. eCollection 2020.
6
Up-regulated cytotrophoblast DOCK4 contributes to over-invasion in placenta accreta spectrum.
Proc Natl Acad Sci U S A. 2020 Jul 7;117(27):15852-15861. doi: 10.1073/pnas.1920776117. Epub 2020 Jun 23.
8
Inhibition of glioma proliferation and migration by magnetic nanoparticle mediated JAM-2 silencing.
J Mater Chem B. 2014 Nov 7;2(41):7168-7175. doi: 10.1039/c4tb00954a. Epub 2014 Sep 17.
9
The JAM-B/c-src/MMP9 pathway is associated with progression and regulates the invasion of pancreatic cancer.
J Cancer. 2020 Mar 5;11(11):3246-3255. doi: 10.7150/jca.40953. eCollection 2020.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验