LIF-STAT in decidual cells: possible role in embryo implantation and early pregnancy

蜕膜 细胞生物学 间质细胞 细胞粘附分子 蜕膜细胞 小RNA 滋养层 化学 炎症体 细胞粘附 胚胎 生物 癌症研究 粘附 免疫学 炎症 怀孕 胎盘 胎儿 生物化学 遗传学 有机化学 基因
作者
Hsien‐Ming Wu,Liang‐Hsuan Chen,Wei‐Jung Chiu,Chia-Lung Tsai
出处
期刊:Journal of Molecular Endocrinology [Bioscientifica]
卷期号:73 (2) 被引量:1
标识
DOI:10.1530/jme-24-0006
摘要

In this study, we investigate the effects of miRNA-138-5p and probable G-protein coupled receptor 124 (GPR124)-regulated inflammasome and downstream leukemia inhibitory factor (LIF)-STAT and adhesion molecule signaling in human decidual stromal cells. After informed consent was obtained from women aged 25-38 years undergoing surgical termination of the normal pregnancy and spontaneous miscarriage after 6-9 weeks of gestation, human decidual stromal cells were extracted from the decidual tissue. Extracellular vesicles (EVs) with microRNA (miRNA) between cells have been regarded as critical factors for embryo-maternal interactions on embryo implantation and programming of human pregnancy. MicroRNA-138-5p acts as the transcriptional regulator of GPR124 and the mediator of downstream inflammasome. LIF-regulated STAT activation and expression of integrins might influence embryo implantation. Hence, a better understanding of LIF-STAT and adhesion molecule signaling would elucidate the mechanism of microRNA-138-5p- and GPR124-regulated inflammasome activation on embryo implantation and pregnancy. Our results show that microRNA-138-5p, purified from the EVs of decidual stromal cells, inhibits the expression of GPR124 and the inflammasome, and activates the expression of LIF-STAT and adhesion molecules in human decidual stromal cells. Additionally, the knockdown of GPR124 and NLRP3 through siRNA increases the expression of LIF-STAT and adhesion molecules. The findings of this study help us gain a better understanding the role of EVs, microRNA-138-5p, GPR124, inflammasomes, LIF-STAT, and adhesion molecules in embryo implantation and programming of human pregnancy.

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