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Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity

BACKGROUND: The establishment of uterine receptivity is essential for embryo implantation initiation and involves a significant morphological transformation in the endometrial epithelial cells (EECs). The remodeling of junctional complexes and membrane-associated cytoskeleton is crucial for epitheli...

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Autores principales: Liang, Jingjie, Li, Kui, Chen, Kaiyu, Liang, Junyong, Qin, Ti, He, Jiayi, Shi, Shuang, Tan, Qiang, Wang, Zhengguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788769/
https://www.ncbi.nlm.nih.gov/pubmed/33407571
http://dx.doi.org/10.1186/s12958-020-00689-7
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author Liang, Jingjie
Li, Kui
Chen, Kaiyu
Liang, Junyong
Qin, Ti
He, Jiayi
Shi, Shuang
Tan, Qiang
Wang, Zhengguang
author_facet Liang, Jingjie
Li, Kui
Chen, Kaiyu
Liang, Junyong
Qin, Ti
He, Jiayi
Shi, Shuang
Tan, Qiang
Wang, Zhengguang
author_sort Liang, Jingjie
collection PubMed
description BACKGROUND: The establishment of uterine receptivity is essential for embryo implantation initiation and involves a significant morphological transformation in the endometrial epithelial cells (EECs). The remodeling of junctional complexes and membrane-associated cytoskeleton is crucial for epithelial transformation. However, little is known about how this process is regulated in EECs during the receptive phase. ARHGAP19 is a Rho GTPase-activating protein that participates in various cytoskeletal-related events, including epithelial morphogenesis. Here, we investigated the role of ARHGAP19 in endometrial epithelial transformation during the establishment of uterine receptivity. The upstream regulator of ARHGAP19 was also investigated. METHODS: ARHGAP19 expression was examined in mouse uteri during early pregnancy and in human EEC lines. The role of ARHGAP19 was investigated by manipulating its expression in EECs. The effect of ARHGAP19 on junctional proteins in EECs was examined by western blotting and immunofluorescence. The effect of ARHGAP19 on microvilli was examined by scanning electron microscopy. The upstream microRNA (miRNA) was predicted using online databases and validated by the dual-luciferase assay. The in vivo and in vitro effect of miRNA on endogenous ARHGAP19 was examined by uterine injection of miRNA agomirs and transfection of miRNA mimics or inhibitors. RESULTS: ARHGAP19 was upregulated in the receptive mouse uteri and human EECs. Overexpression of ARHGAP19 in non-receptive EECs downregulated the expression of junctional proteins and resulted in their redistribution. Meanwhile, upregulating ARHGAP19 reorganized the cytoskeletal structure of EECs, leading to a decline of microvilli and changes in cell configuration. These changes weakened epithelial cell polarity and promoted the transition of non-receptive EECs to a receptive phenotype. Besides, miR-192-5p, a miRNA that plays a key role in maintaining epithelial properties, was validated as an upstream regulator of ARHGAP19. CONCLUSION: These results suggested that ARHGAP19 may contribute to the transition of EECs from a non-receptive to a receptive state by regulating the remodeling of junctional proteins and membrane-associated cytoskeleton.
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spelling pubmed-77887692021-01-07 Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity Liang, Jingjie Li, Kui Chen, Kaiyu Liang, Junyong Qin, Ti He, Jiayi Shi, Shuang Tan, Qiang Wang, Zhengguang Reprod Biol Endocrinol Research BACKGROUND: The establishment of uterine receptivity is essential for embryo implantation initiation and involves a significant morphological transformation in the endometrial epithelial cells (EECs). The remodeling of junctional complexes and membrane-associated cytoskeleton is crucial for epithelial transformation. However, little is known about how this process is regulated in EECs during the receptive phase. ARHGAP19 is a Rho GTPase-activating protein that participates in various cytoskeletal-related events, including epithelial morphogenesis. Here, we investigated the role of ARHGAP19 in endometrial epithelial transformation during the establishment of uterine receptivity. The upstream regulator of ARHGAP19 was also investigated. METHODS: ARHGAP19 expression was examined in mouse uteri during early pregnancy and in human EEC lines. The role of ARHGAP19 was investigated by manipulating its expression in EECs. The effect of ARHGAP19 on junctional proteins in EECs was examined by western blotting and immunofluorescence. The effect of ARHGAP19 on microvilli was examined by scanning electron microscopy. The upstream microRNA (miRNA) was predicted using online databases and validated by the dual-luciferase assay. The in vivo and in vitro effect of miRNA on endogenous ARHGAP19 was examined by uterine injection of miRNA agomirs and transfection of miRNA mimics or inhibitors. RESULTS: ARHGAP19 was upregulated in the receptive mouse uteri and human EECs. Overexpression of ARHGAP19 in non-receptive EECs downregulated the expression of junctional proteins and resulted in their redistribution. Meanwhile, upregulating ARHGAP19 reorganized the cytoskeletal structure of EECs, leading to a decline of microvilli and changes in cell configuration. These changes weakened epithelial cell polarity and promoted the transition of non-receptive EECs to a receptive phenotype. Besides, miR-192-5p, a miRNA that plays a key role in maintaining epithelial properties, was validated as an upstream regulator of ARHGAP19. CONCLUSION: These results suggested that ARHGAP19 may contribute to the transition of EECs from a non-receptive to a receptive state by regulating the remodeling of junctional proteins and membrane-associated cytoskeleton. BioMed Central 2021-01-07 /pmc/articles/PMC7788769/ /pubmed/33407571 http://dx.doi.org/10.1186/s12958-020-00689-7 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liang, Jingjie
Li, Kui
Chen, Kaiyu
Liang, Junyong
Qin, Ti
He, Jiayi
Shi, Shuang
Tan, Qiang
Wang, Zhengguang
Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title_full Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title_fullStr Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title_full_unstemmed Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title_short Regulation of ARHGAP19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
title_sort regulation of arhgap19 in the endometrial epithelium: a possible role in the establishment of uterine receptivity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788769/
https://www.ncbi.nlm.nih.gov/pubmed/33407571
http://dx.doi.org/10.1186/s12958-020-00689-7
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