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The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes
BACKGROUND: Implantation failure limits the success of in vitro fertilization and embryo transfer (IVF-ET). Well-organized embryo-maternal crosstalk is essential for successful implantation. Previous studies mainly focused on the aberrant development of in vitro fertilized (IVF) embryos. In contrast...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958772/ https://www.ncbi.nlm.nih.gov/pubmed/31956410 http://dx.doi.org/10.1186/s40104-019-0405-y |
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author | Yang, Qianying Fu, Wei Wang, Yue Miao, Kai Zhao, Haichao Wang, Rui Guo, Min Wang, Zhilong Tian, Jianhui An, Lei |
author_facet | Yang, Qianying Fu, Wei Wang, Yue Miao, Kai Zhao, Haichao Wang, Rui Guo, Min Wang, Zhilong Tian, Jianhui An, Lei |
author_sort | Yang, Qianying |
collection | PubMed |
description | BACKGROUND: Implantation failure limits the success of in vitro fertilization and embryo transfer (IVF-ET). Well-organized embryo-maternal crosstalk is essential for successful implantation. Previous studies mainly focused on the aberrant development of in vitro fertilized (IVF) embryos. In contrast, the mechanism of IVF-induced aberrant embryo-maternal crosstalk is not well defined. RESULTS: In the present study, using ewes as the model, we profiled the proteome that features aberrant IVF embryo-maternal crosstalk following IVF-ET. By comparing in vivo (IVO) and IVF conceptuses, as well as matched endometrial caruncular (C) and intercaruncular (IC) areas, we filtered out 207, 295, and 403 differentially expressed proteins (DEPs) in each comparison. Proteome functional analysis showed that the IVF conceptuses were characterized by the increased abundance of energy metabolism and proliferation-related proteins, and the decreased abundance of methyl metabolism-related proteins. In addition, IVF endometrial C areas showed the decreased abundance of endometrial remodeling and redox homeostasis-related proteins; while IC areas displayed the aberrant abundance of protein homeostasis and extracellular matrix (ECM) interaction-related proteins. Based on these observations, we propose a model depicting the disrupted embryo-maternal crosstalk following IVF-ET: Aberrant energy metabolism and redox homeostasis of IVF embryos, might lead to an aberrant endometrial response to conceptus-derived pregnancy signals, thus impairing maternal receptivity. In turn, the suboptimal uterine environment might stimulate a compensation effect of the IVF conceptuses, which was revealed as enhanced energy metabolism and over-proliferation. CONCLUSION: Systematic proteomic profiling provides insights to understand the mechanisms that underlie the aberrant IVF embryo-maternal crosstalk. This might be helpful to develop practical strategies to prevent implantation failure following IVF-ET. |
format | Online Article Text |
id | pubmed-6958772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69587722020-01-17 The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes Yang, Qianying Fu, Wei Wang, Yue Miao, Kai Zhao, Haichao Wang, Rui Guo, Min Wang, Zhilong Tian, Jianhui An, Lei J Anim Sci Biotechnol Research BACKGROUND: Implantation failure limits the success of in vitro fertilization and embryo transfer (IVF-ET). Well-organized embryo-maternal crosstalk is essential for successful implantation. Previous studies mainly focused on the aberrant development of in vitro fertilized (IVF) embryos. In contrast, the mechanism of IVF-induced aberrant embryo-maternal crosstalk is not well defined. RESULTS: In the present study, using ewes as the model, we profiled the proteome that features aberrant IVF embryo-maternal crosstalk following IVF-ET. By comparing in vivo (IVO) and IVF conceptuses, as well as matched endometrial caruncular (C) and intercaruncular (IC) areas, we filtered out 207, 295, and 403 differentially expressed proteins (DEPs) in each comparison. Proteome functional analysis showed that the IVF conceptuses were characterized by the increased abundance of energy metabolism and proliferation-related proteins, and the decreased abundance of methyl metabolism-related proteins. In addition, IVF endometrial C areas showed the decreased abundance of endometrial remodeling and redox homeostasis-related proteins; while IC areas displayed the aberrant abundance of protein homeostasis and extracellular matrix (ECM) interaction-related proteins. Based on these observations, we propose a model depicting the disrupted embryo-maternal crosstalk following IVF-ET: Aberrant energy metabolism and redox homeostasis of IVF embryos, might lead to an aberrant endometrial response to conceptus-derived pregnancy signals, thus impairing maternal receptivity. In turn, the suboptimal uterine environment might stimulate a compensation effect of the IVF conceptuses, which was revealed as enhanced energy metabolism and over-proliferation. CONCLUSION: Systematic proteomic profiling provides insights to understand the mechanisms that underlie the aberrant IVF embryo-maternal crosstalk. This might be helpful to develop practical strategies to prevent implantation failure following IVF-ET. BioMed Central 2020-01-14 /pmc/articles/PMC6958772/ /pubmed/31956410 http://dx.doi.org/10.1186/s40104-019-0405-y Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Yang, Qianying Fu, Wei Wang, Yue Miao, Kai Zhao, Haichao Wang, Rui Guo, Min Wang, Zhilong Tian, Jianhui An, Lei The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title | The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title_full | The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title_fullStr | The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title_full_unstemmed | The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title_short | The proteome of IVF-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
title_sort | proteome of ivf-induced aberrant embryo-maternal crosstalk by implantation stage in ewes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958772/ https://www.ncbi.nlm.nih.gov/pubmed/31956410 http://dx.doi.org/10.1186/s40104-019-0405-y |
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