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Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy
During pregnancy, the uterus undergoes intense neovascularization and vascular remodeling to supply oxygen and nutrients to the embryo. During this period, progesterone secreted from the ovary has effects on vascular remodeling in the endometrium and interacts with angiogenic factors. However, the e...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339584/ https://www.ncbi.nlm.nih.gov/pubmed/32468067 http://dx.doi.org/10.3892/mmr.2020.11185 |
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author | Park, Yang-Gyu Choi, Jawun Seol, Jae-Won |
author_facet | Park, Yang-Gyu Choi, Jawun Seol, Jae-Won |
author_sort | Park, Yang-Gyu |
collection | PubMed |
description | During pregnancy, the uterus undergoes intense neovascularization and vascular remodeling to supply oxygen and nutrients to the embryo. During this period, progesterone secreted from the ovary has effects on vascular remodeling in the endometrium and interacts with angiogenic factors. However, the exact mechanism of uterine vascular remodeling during pregnancy is poorly understood. Therefore, the aim of the present study was to investigate the association between angiopoietin-2 (Ang-2), one of the angiopoietins, and intrauterine vessel remodeling during pregnancy, and to determine the effect of progesterone on Ang-2 levels. Changes in Ang-2 expression were observed according to quantitative modification of progesterone using pregnant mice and human uterine microvascular endothelial cells. As a result, Ang-2 was observed mainly in the mesometrial region (MR) of the uterus during the period between implantation and placentation. Furthermore, a substantial amount of Ang-2 also appeared in endothelial cells, particularly of the venous sinus region (VSR). Interestingly, Ang-2 expression was increased by progesterone, whereas estrogen had limited effects. To confirm the association between Ang-2 and progesterone, the function of the progesterone receptor (PR) was inhibited using RU486, a blocker of PR. Ang-2 expression and vascular remodeling of the VSR in the uterus were decreased when the functions of progesterone were inhibited. Overall, the regulation of Ang-2 by progesterone/PR was associated with vascular remodeling in the VSR during pregnancy. The present study proposed a solution to prevent pregnancy failure due to a lack of vascularity in the uterus in advance. |
format | Online Article Text |
id | pubmed-7339584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-73395842020-07-09 Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy Park, Yang-Gyu Choi, Jawun Seol, Jae-Won Mol Med Rep Articles During pregnancy, the uterus undergoes intense neovascularization and vascular remodeling to supply oxygen and nutrients to the embryo. During this period, progesterone secreted from the ovary has effects on vascular remodeling in the endometrium and interacts with angiogenic factors. However, the exact mechanism of uterine vascular remodeling during pregnancy is poorly understood. Therefore, the aim of the present study was to investigate the association between angiopoietin-2 (Ang-2), one of the angiopoietins, and intrauterine vessel remodeling during pregnancy, and to determine the effect of progesterone on Ang-2 levels. Changes in Ang-2 expression were observed according to quantitative modification of progesterone using pregnant mice and human uterine microvascular endothelial cells. As a result, Ang-2 was observed mainly in the mesometrial region (MR) of the uterus during the period between implantation and placentation. Furthermore, a substantial amount of Ang-2 also appeared in endothelial cells, particularly of the venous sinus region (VSR). Interestingly, Ang-2 expression was increased by progesterone, whereas estrogen had limited effects. To confirm the association between Ang-2 and progesterone, the function of the progesterone receptor (PR) was inhibited using RU486, a blocker of PR. Ang-2 expression and vascular remodeling of the VSR in the uterus were decreased when the functions of progesterone were inhibited. Overall, the regulation of Ang-2 by progesterone/PR was associated with vascular remodeling in the VSR during pregnancy. The present study proposed a solution to prevent pregnancy failure due to a lack of vascularity in the uterus in advance. D.A. Spandidos 2020-08 2020-05-27 /pmc/articles/PMC7339584/ /pubmed/32468067 http://dx.doi.org/10.3892/mmr.2020.11185 Text en Copyright: © Park et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Park, Yang-Gyu Choi, Jawun Seol, Jae-Won Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title | Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title_full | Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title_fullStr | Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title_full_unstemmed | Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title_short | Angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
title_sort | angiopoietin-2 regulated by progesterone induces uterine vascular remodeling during pregnancy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339584/ https://www.ncbi.nlm.nih.gov/pubmed/32468067 http://dx.doi.org/10.3892/mmr.2020.11185 |
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