Metabolic reprogramming and heterogeneity during the decidualization process of endometrial stromal cells.

IF 8.2 2区 生物学 Q1 CELL BIOLOGY
Zhaoyu Jia, Yuan Wei, Ye Zhang, Kun Song, Jia Yuan
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引用次数: 0

Abstract

The human endometrial decidualization is a transformative event in the pregnant uterus that involves the differentiation of stromal cells into decidual cells. While crucial to the establishment of a successful pregnancy, the metabolic characteristics of decidual cells in vivo remain largely unexplored. Here, we integrated the single-cell RNA sequencing (scRNA-seq) datasets on the endometrium of the menstrual cycle and the maternal-fetal interface in the first trimester to comprehensively decrypt the metabolic characteristics of stromal fibroblast cells. Our results revealed that the differentiation of stromal cells into decidual cells is accompanied by increased amino acid and sphingolipid metabolism. Furthermore, metabolic heterogeneity exists in decidual cells with differentiation maturity disparities. Decidual cells with high metabolism exhibit higher cellular activity and show a strong propensity for signaling. In addition, significant metabolic reprogramming in amino acids and lipids also occurs during the transition from non-pregnancy to pregnancy in the uteri of pigs, cattle, and mice. Our analysis provides comprehensive insights into the dynamic landscape of stromal fibroblast cell metabolism, contributing to our understanding of the metabolism at the molecular dynamics underlying the decidualization process in the human endometrium.

子宫内膜基质细胞蜕膜化过程中的代谢重编程和异质性。
人类子宫内膜蜕膜化是妊娠子宫的一个转变过程,包括基质细胞向蜕膜细胞的分化。虽然蜕膜细胞对成功怀孕至关重要,但它们在体内的新陈代谢特征在很大程度上仍未得到研究。在这里,我们整合了月经周期子宫内膜和妊娠头三个月母胎界面的单细胞RNA测序(scRNA-seq)数据集,全面解密了基质成纤维细胞的代谢特征。我们的研究结果表明,基质细胞向蜕膜细胞分化的过程中氨基酸和鞘脂代谢增加。此外,蜕膜细胞的代谢异质性与分化成熟度存在差异。新陈代谢旺盛的蜕膜细胞表现出更高的细胞活性,并显示出强烈的信号传导倾向。此外,在猪、牛和小鼠的子宫从非妊娠期向妊娠期过渡的过程中,氨基酸和脂质的代谢也发生了显著的重编程。我们的分析全面揭示了基质成纤维细胞新陈代谢的动态变化,有助于我们了解人类子宫内膜蜕膜化过程的分子动态新陈代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
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