Urothelial Cancer Associated 1 (UCA1) and miR-193 Are Two Non-coding RNAs Involved in Trophoblast Fusion and Placental Diseases

被引:11
作者
Apicella, Clara [1 ]
Ruano, Camino S. M. [1 ]
Jacques, Sebastien [1 ]
Gascoin, Geraldine [2 ,3 ]
Mehats, Celine [1 ]
Vaiman, Daniel [1 ]
Miralles, Francisco [1 ]
机构
[1] Univ Paris, CNRS, Inst Cochin, INSERM,UMR 8104,U1016, Paris, France
[2] Univ Angers, CNRS 6015, Unite Mixte Rech MITOVASC, Equipe Mitolab,INSERM,U1083, Angers, France
[3] Ctr Hosp Univ, Reanimat & Med Neonatales, Angers, France
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 9卷
基金
欧盟地平线“2020”;
关键词
trophoblast; placenta; preeclampsia; intra uterine growth restriction; syncytialisation; non-coding RNAs; INTRAUTERINE GROWTH RESTRICTION; GENE-EXPRESSION; INHIBITS APOPTOSIS; CELL-PROLIFERATION; PREECLAMPSIA; CHORIOCARCINOMA; STOX1; MICRORNAS; SYNCYTIUM; SYNCYTIALIZATION;
D O I
10.3389/fcell.2021.633937
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A bioinformatics screen for non-coding genes was performed from microarrays analyzing on the one hand trophoblast fusion in the BeWo cell model, and on the other hand, placental diseases (preeclampsia and Intra-Uterine Growth Restriction). Intersecting the deregulated genes allowed to identify two miRNA (mir193b and miR365a) and one long non-coding RNA (UCA1) that are pivotal for trophoblast fusion, and deregulated in placental diseases. We show that miR-193b is a hub for the down-regulation of 135 cell targets mainly involved in cell cycle progression and energy usage/nutrient transport. UCA1 was explored by siRNA knock-down in the BeWo cell model. We show that its down-regulation is associated with the deregulation of important trophoblast physiology genes, involved in differentiation, proliferation, oxidative stress, vacuolization, membrane repair and endocrine production. Overall, UCA1 knockdown leads to an incomplete gene expression profile modification of trophoblast cells when they are induced to fuse into syncytiotrophoblast. Then we performed the same type of analysis in cells overexpressing one of the two major isoforms of the STOX1 transcription factor, STOX1A and STOX1B (associated previously to impaired trophoblast fusion). We could show that when STOX1B is abundant, the effects of UCA1 down-regulation on forskolin response are alleviated.
引用
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页数:16
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