Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol

Abstract Background Uterine receptivity is one of the determinants of embryo implantation, which is responsible for pregnancy success. Aberrant embryo implantation due to disrupted uterine receptivity is usually found in ovarian hyperstimulation induced hyperoestrogen patients. Results This study id...

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Main Authors: He Zhang, Huashan Zhao, Xi Wang, Xiaolin Cui, Lingling Jin
Format: Article
Language:English
Published: BMC 2020-02-01
Series:BMC Developmental Biology
Subjects:
Online Access:https://doi.org/10.1186/s12861-020-0208-6
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spelling doaj-cc07e2bf71cb457f9f9a973371cc24432021-02-07T12:25:14ZengBMCBMC Developmental Biology1471-213X2020-02-012011810.1186/s12861-020-0208-6Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiolHe Zhang0Huashan Zhao1Xi Wang2Xiaolin Cui3Lingling Jin4College of Basic Medical Sciences, Dalian Medical UniversityCenter for Reproduction and Health Development, Shenzhen Institutes of Advanced Technology, Chinese Academy of SciencesCollege of Basic Medical Sciences, Dalian Medical UniversityCollege of Basic Medical Sciences, Dalian Medical UniversityCollege of Basic Medical Sciences, Dalian Medical UniversityAbstract Background Uterine receptivity is one of the determinants of embryo implantation, which is responsible for pregnancy success. Aberrant embryo implantation due to disrupted uterine receptivity is usually found in ovarian hyperstimulation induced hyperoestrogen patients. Results This study identified keratin 86 (KRT86), a fibrous structural protein, which was upregulated in uterine endometrium during peri-implantation. Using a hyperoestrogen mouse model established in a previous study, we found abnormal oestradiol (E2) levels during pre-implantation could trigger high expression of Krt86 in the uterine epithelium. In an ovariectomised mouse model, combining oestrogen receptors ERα and ERβ knockout mice models, uterine Krt86 was found to be up-regulated after E2 treatment, mediated by nuclear ERα. Furthermore, we found progesterone (P4) could ameliorate Krt86 expression, induced by abnormal E2. Conclusions These results revealed the dynamic expression and regulation of Krt86, especially in hyperoestrogen treated mice, indicating it might act as a marker for non-receptive uterus.https://doi.org/10.1186/s12861-020-0208-6ImplantationUterusOestrogenProgesteroneKeratin 86
collection DOAJ
language English
format Article
sources DOAJ
author He Zhang
Huashan Zhao
Xi Wang
Xiaolin Cui
Lingling Jin
spellingShingle He Zhang
Huashan Zhao
Xi Wang
Xiaolin Cui
Lingling Jin
Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
BMC Developmental Biology
Implantation
Uterus
Oestrogen
Progesterone
Keratin 86
author_facet He Zhang
Huashan Zhao
Xi Wang
Xiaolin Cui
Lingling Jin
author_sort He Zhang
title Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
title_short Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
title_full Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
title_fullStr Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
title_full_unstemmed Keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
title_sort keratin 86 is up-regulated in the uterus during implantation, induced by oestradiol
publisher BMC
series BMC Developmental Biology
issn 1471-213X
publishDate 2020-02-01
description Abstract Background Uterine receptivity is one of the determinants of embryo implantation, which is responsible for pregnancy success. Aberrant embryo implantation due to disrupted uterine receptivity is usually found in ovarian hyperstimulation induced hyperoestrogen patients. Results This study identified keratin 86 (KRT86), a fibrous structural protein, which was upregulated in uterine endometrium during peri-implantation. Using a hyperoestrogen mouse model established in a previous study, we found abnormal oestradiol (E2) levels during pre-implantation could trigger high expression of Krt86 in the uterine epithelium. In an ovariectomised mouse model, combining oestrogen receptors ERα and ERβ knockout mice models, uterine Krt86 was found to be up-regulated after E2 treatment, mediated by nuclear ERα. Furthermore, we found progesterone (P4) could ameliorate Krt86 expression, induced by abnormal E2. Conclusions These results revealed the dynamic expression and regulation of Krt86, especially in hyperoestrogen treated mice, indicating it might act as a marker for non-receptive uterus.
topic Implantation
Uterus
Oestrogen
Progesterone
Keratin 86
url https://doi.org/10.1186/s12861-020-0208-6
work_keys_str_mv AT hezhang keratin86isupregulatedintheuterusduringimplantationinducedbyoestradiol
AT huashanzhao keratin86isupregulatedintheuterusduringimplantationinducedbyoestradiol
AT xiwang keratin86isupregulatedintheuterusduringimplantationinducedbyoestradiol
AT xiaolincui keratin86isupregulatedintheuterusduringimplantationinducedbyoestradiol
AT linglingjin keratin86isupregulatedintheuterusduringimplantationinducedbyoestradiol
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