Associations between maternal plasma concentrations of corticotrophin releasing hormone and the placental transcriptome

IF 3 2区 医学 Q2 DEVELOPMENTAL BIOLOGY Placenta Pub Date : 2025-02-01 DOI:10.1016/j.placenta.2024.12.021
Alison Paquette , Mariana Parenti , Samantha Lapehn , Chaini Konwar , Leena Kadam , Evan J. Firsick , Emily S. Barrett , Julie MacIsaac , James MacDonald , Theo Bammler , Kecia Carroll , Daniel Enquobahrie , Michael Kobor , Kaja Z. LeWinn , Ruby Nguyen , Roger Smith , Adam Spirzo , Qi Zhao , Leslie Myatt , Nicole R. Bush , Sheela Sathyanarayana
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Abstract

Introduction

The placenta produces corticotrophin releasing hormone (CRH), which rises exponentially in maternal plasma across pregnancy. CRH plays a functional role in fetal development, labor initiation, and the regulation of gestational length. We aimed to understand how maternal plasma CRH during pregnancy reflects placental physiology during parturition by characterizing placental transcriptomic signatures of maternal plasma CRH and comparing to transcriptomic signatures of gestational age at birth.

Methods

Maternal plasma CRH concentrations were measured via radioimmunoassay at two timepoints and the placental transcriptome was quantified via RNA sequencing in 516 pregnant participants enrolled in the CANDLE cohort. Robust linear models were fitted to estimate associations between CRH and placental gene expression at birth. We conducted a functional validation in primary trophoblast cells before and after syncytialization.

Results

Plasma CRH concentrations in the mid-pregnancy visit were associated with placental expression of 8 differentially expressed genes (DEGs), and concentrations in late pregnancy were associated with 283 DEGs. These genes were involved in several metabolic pathways. Seven genes were significantly associated with both plasma CRH and gestational length. Four genes were concordantly decreased and 7 genes were concordantly increased in primary trophoblasts treated with CRH.

Discussion

Overall, this study reveals potential novel transcriptional mechanisms by which CRH may regulate metabolic pathways important for placental function and identifies genes associated with both CRH and gestational length.
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母体血浆促肾上腺皮质激素释放激素浓度与胎盘转录组的关系。
胎盘产生促肾上腺皮质激素释放激素(CRH),在妊娠期间母体血浆中的CRH呈指数级上升。CRH在胎儿发育、分娩起始和妊娠期长短的调节中发挥着功能作用。我们旨在通过分析母体血浆CRH的胎盘转录组特征,并与出生时胎龄的转录组特征进行比较,了解妊娠期母体血浆CRH如何反映分娩期间的胎盘生理。方法:通过放射免疫法在两个时间点测量孕妇血浆CRH浓度,并通过RNA测序对516名参加CANDLE队列的孕妇的胎盘转录组进行量化。拟合了稳健的线性模型来估计CRH与出生时胎盘基因表达之间的关系。我们在原代滋养细胞合胞前后进行了功能验证。结果:妊娠中期血浆CRH浓度与胎盘8个差异表达基因(DEGs)表达相关,妊娠晚期血浆CRH浓度与283个差异表达基因(DEGs)表达相关。这些基因参与了几种代谢途径。7个基因与血浆CRH和妊娠期长度均显著相关。CRH处理的原代滋养细胞中有4个基因一致降低,7个基因一致升高。讨论:总的来说,这项研究揭示了潜在的新的转录机制,通过该机制CRH可能调节对胎盘功能重要的代谢途径,并确定了与CRH和妊娠长度相关的基因。
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来源期刊
Placenta
Placenta 医学-发育生物学
CiteScore
6.30
自引率
10.50%
发文量
391
审稿时长
78 days
期刊介绍: Placenta publishes high-quality original articles and invited topical reviews on all aspects of human and animal placentation, and the interactions between the mother, the placenta and fetal development. Topics covered include evolution, development, genetics and epigenetics, stem cells, metabolism, transport, immunology, pathology, pharmacology, cell and molecular biology, and developmental programming. The Editors welcome studies on implantation and the endometrium, comparative placentation, the uterine and umbilical circulations, the relationship between fetal and placental development, clinical aspects of altered placental development or function, the placental membranes, the influence of paternal factors on placental development or function, and the assessment of biomarkers of placental disorders.
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