LncRNA MEG3 inhibits trophoblast invasion and trophoblast‐mediated VSMC loss in uterine spiral artery remodeling

2019 ◽  
Vol 86 (6) ◽  
pp. 686-695 ◽  
Author(s):  
Hui Tao ◽  
Xiaoping Liu ◽  
Xiaoxia Liu ◽  
Weifang Liu ◽  
Di Wu ◽  
...  
Keyword(s):  
Trophoblast Invasion ◽  
Spiral Artery ◽  
Artery Remodeling

Extracellular ATP decreases trophoblast invasion, spiral artery remodeling and immune cells in the mesometrial triangle in pregnant rats

Placenta ◽  
2014 ◽  
Vol 35 (8) ◽  
pp. 587-595 ◽  
Author(s):  
F. Spaans ◽  
B.N. Melgert ◽  
C. Chiang ◽  
T. Borghuis ◽  
P.A. Klok ◽  
...  
Keyword(s):  
Immune Cells ◽  
Extracellular Atp ◽  
Trophoblast Invasion ◽  
Spiral Artery ◽  
Pregnant Rats ◽  
Artery Remodeling

Angiopoietin 2 stimulates trophoblast invasion via a mechanism associated with JNK signaling

2021 ◽  
Author(s):  
Huomei Hou ◽  
Fen Ning ◽  
Joy Yue Zhang ◽  
Qinsheng Lu ◽  
Min Zhang ◽  
...  
Keyword(s):  
Trophoblast Cell ◽  
Extravillous Trophoblast ◽  
Trophoblast Invasion ◽  
Integrin Signaling ◽  
Spiral Artery ◽  
Trophoblast Cells ◽  
Jnk Signaling ◽  
Tie2 Receptor ◽  
Artery Remodeling ◽  
Angiopoietin 2

Abstract Extravillous trophoblast cell (EVT) invasion is tightly controlled, and its dysregulation can lead to altered spiral artery remodeling and contribute to a number of different pregnancy complications. Angiopoietin-2 (Ang-2) is expressed by trophoblast cells and various cells in the decidua, and trophoblast cells express its receptor, Tie2. Ang-2 has been shown to play roles in tumor progression and metastasis but it is not known if it also regulates EVT invasion. Here we show that both the HTR-8/SVneo cell line and primary isolates of human EVT expressed various integrins and the Tie2 receptor, and Ang-2 stimulated their migration and/or invasion. Ang-2 increased expression of matrix metalloproteinase (MMP)2 and MMP9, altered the cytoskeleton of HTR-8/SVneo cells and also induced phosphorylation of Tie2, JNK and c-Jun. Inhibition of p-JNK (using SP600125) blocked the Ang-2 induced invasion of HTR-8/SVneo cells. In addition, inhibition of Tie2 (pexmetinib) and integrin signaling (RGDS and ATN-161) also blocked Ang-2 induced invasion. In conclusion, we demonstrate that Ang-2 can stimulate EVT invasion via a mechanism associated with activation of both the Tie2 receptor and integrins, which appear to work through different pathways; Tie2 through the JNK/c-JUN pathway and integrins through an as yet unidentified pathway(s). We therefore propose that any alterations in Ang-2 expression in the decidua would lead to an imbalance in pro- and anti-invasive factors, disrupting regulation of EVT invasion and spiral artery remodeling and thereby contribute to the aetiology of several complications of pregnancy.

scholarly journals HIF-KDM3A-MMP12 regulatory circuit ensures trophoblast plasticity and placental adaptations to hypoxia

2016 ◽  
Vol 113 (46) ◽  
pp. E7212-E7221 ◽  
Author(s):  
Damayanti Chakraborty ◽  
Wei Cui ◽  
Gracy X. Rosario ◽  
Regan L. Scott ◽  
Pramod Dhakal ◽  
...  
Keyword(s):  
Genome Editing ◽  
Methylation Status ◽  
Trophoblast Cell ◽  
Trophoblast Invasion ◽  
Spiral Artery ◽  
Low Oxygen ◽  
Transcription Activator ◽  
Regulatory Circuit ◽  
Artery Remodeling

The hemochorial placenta develops from the coordinated multilineage differentiation of trophoblast stem (TS) cells. An invasive trophoblast cell lineage remodels uterine spiral arteries, facilitating nutrient flow, failure of which is associated with pathological conditions such as preeclampsia, intrauterine growth restriction, and preterm birth. Hypoxia plays an instructive role in influencing trophoblast cell differentiation and regulating placental organization. Key downstream hypoxia-activated events were delineated using rat TS cells and tested in vivo, using trophoblast-specific lentiviral gene delivery and genome editing. DNA microarray analyses performed on rat TS cells exposed to ambient or low oxygen and pregnant rats exposed to ambient or hypoxic conditions showed up-regulation of genes characteristic of an invasive/vascular remodeling/inflammatory phenotype. Among the shared up-regulated genes was matrix metallopeptidase 12 (MMP12). To explore the functional importance of MMP12 in trophoblast cell-directed spiral artery remodeling, we generated an Mmp12 mutant rat model using transcription activator-like nucleases-mediated genome editing. Homozygous mutant placentation sites showed decreased hypoxia-dependent endovascular trophoblast invasion and impaired trophoblast-directed spiral artery remodeling. A link was established between hypoxia/HIF and MMP12; however, evidence did not support Mmp12 as a direct target of HIF action. Lysine demethylase 3A (KDM3A) was identified as mediator of hypoxia/HIF regulation of Mmp12. Knockdown of KDM3A in rat TS cells inhibited the expression of a subset of the hypoxia–hypoxia inducible factor (HIF)-dependent transcripts, including Mmp12, altered H3K9 methylation status, and decreased hypoxia-induced trophoblast cell invasion in vitro and in vivo. The hypoxia-HIF-KDM3A-MMP12 regulatory circuit is conserved and facilitates placental adaptations to environmental challenges.

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