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Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period

Recent studies indicate that FoxO1 has roles in female reproductive system, especially in maternal endometrium. Although various cellular aspects and molecular pathways have been identified, the exact molecular characteristics of embryo implantation are still not completely understood. In this study...

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Autores principales: Adiguzel, Dileyra, Sahin, Pinar, Kuscu, Nilay, Ozkavukcu, Sinan, Bektas, Nayce Ilayda, Celik-Ozenci, Ciler
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532854/
https://www.ncbi.nlm.nih.gov/pubmed/31120913
http://dx.doi.org/10.1371/journal.pone.0216814
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author Adiguzel, Dileyra
Sahin, Pinar
Kuscu, Nilay
Ozkavukcu, Sinan
Bektas, Nayce Ilayda
Celik-Ozenci, Ciler
author_facet Adiguzel, Dileyra
Sahin, Pinar
Kuscu, Nilay
Ozkavukcu, Sinan
Bektas, Nayce Ilayda
Celik-Ozenci, Ciler
author_sort Adiguzel, Dileyra
collection PubMed
description Recent studies indicate that FoxO1 has roles in female reproductive system, especially in maternal endometrium. Although various cellular aspects and molecular pathways have been identified, the exact molecular characteristics of embryo implantation are still not completely understood. In this study, we aimed to investigate uterine expression and regulation of FoxO1 during peri-implantation period in mice. Experimental mouse models including, normal pregnancy, pseudopregnancy, artificial decidualization, and delayed implantation and activation were performed. Our results showed that FoxO1 expression was spatiotemporal in mouse endometrial tissue throughout peri-implantation period and its expression was significantly upregulated in luminal and glandular epithelium at the time of implantation. Moreover, on day 5 morning (09:00 AM) of pregnancy, expression of FoxO1 was cytoplasmic in endometrial luminal epithelial cells where embryo homing takes place. With progressing time on day 5 evening (19:00 PM) of pregnancy FoxO1 expression was nuclear in luminal epithelium at implantation site. Pseudopregnancy and artificial decidualization models indicated that FoxO1 expression was regulated by pregnancy hormones. Delayed implantation and activation model indicated that FoxO1 expression at the time of implantation is dependent upon activation status of blastocyst due to E2 induction and uterine sensitivity to implantation. In conclusion, our findings highlight a perspective for FoxO1 expression and regulation in mouse uterus during peri-implantation period indicating that its expression is regulated by implanting embryo and pregnancy hormones.
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spelling pubmed-65328542019-06-05 Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period Adiguzel, Dileyra Sahin, Pinar Kuscu, Nilay Ozkavukcu, Sinan Bektas, Nayce Ilayda Celik-Ozenci, Ciler PLoS One Research Article Recent studies indicate that FoxO1 has roles in female reproductive system, especially in maternal endometrium. Although various cellular aspects and molecular pathways have been identified, the exact molecular characteristics of embryo implantation are still not completely understood. In this study, we aimed to investigate uterine expression and regulation of FoxO1 during peri-implantation period in mice. Experimental mouse models including, normal pregnancy, pseudopregnancy, artificial decidualization, and delayed implantation and activation were performed. Our results showed that FoxO1 expression was spatiotemporal in mouse endometrial tissue throughout peri-implantation period and its expression was significantly upregulated in luminal and glandular epithelium at the time of implantation. Moreover, on day 5 morning (09:00 AM) of pregnancy, expression of FoxO1 was cytoplasmic in endometrial luminal epithelial cells where embryo homing takes place. With progressing time on day 5 evening (19:00 PM) of pregnancy FoxO1 expression was nuclear in luminal epithelium at implantation site. Pseudopregnancy and artificial decidualization models indicated that FoxO1 expression was regulated by pregnancy hormones. Delayed implantation and activation model indicated that FoxO1 expression at the time of implantation is dependent upon activation status of blastocyst due to E2 induction and uterine sensitivity to implantation. In conclusion, our findings highlight a perspective for FoxO1 expression and regulation in mouse uterus during peri-implantation period indicating that its expression is regulated by implanting embryo and pregnancy hormones. Public Library of Science 2019-05-23 /pmc/articles/PMC6532854/ /pubmed/31120913 http://dx.doi.org/10.1371/journal.pone.0216814 Text en © 2019 Adiguzel et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Adiguzel, Dileyra
Sahin, Pinar
Kuscu, Nilay
Ozkavukcu, Sinan
Bektas, Nayce Ilayda
Celik-Ozenci, Ciler
Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title_full Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title_fullStr Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title_full_unstemmed Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title_short Spatiotemporal expression and regulation of FoxO1 in mouse uterus during peri-implantation period
title_sort spatiotemporal expression and regulation of foxo1 in mouse uterus during peri-implantation period
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532854/
https://www.ncbi.nlm.nih.gov/pubmed/31120913
http://dx.doi.org/10.1371/journal.pone.0216814
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