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Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos

OBJECTIVE: The Hippo pathway plays an important role in embryo development, and separation of trophectoderm (TE) and inner cell mass (ICM) cell lines. Therefore, this study investigated effect of maternal age on activity of Hippo pathway in human embryos. MATERIALS AND METHODS: In this experimental...

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Autores principales: Gharanfoli, Sahar, Shahverdi, Abdolhossein, Dalman, Azam, Ghaznavi, Pooneh, Alipour, Hiva, Eftekhari-Yazdi, Poopak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481894/
https://www.ncbi.nlm.nih.gov/pubmed/32779436
http://dx.doi.org/10.22074/cellj.2020.6860
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author Gharanfoli, Sahar
Shahverdi, Abdolhossein
Dalman, Azam
Ghaznavi, Pooneh
Alipour, Hiva
Eftekhari-Yazdi, Poopak
author_facet Gharanfoli, Sahar
Shahverdi, Abdolhossein
Dalman, Azam
Ghaznavi, Pooneh
Alipour, Hiva
Eftekhari-Yazdi, Poopak
author_sort Gharanfoli, Sahar
collection PubMed
description OBJECTIVE: The Hippo pathway plays an important role in embryo development, and separation of trophectoderm (TE) and inner cell mass (ICM) cell lines. Therefore, this study investigated effect of maternal age on activity of Hippo pathway in human embryos. MATERIALS AND METHODS: In this experimental study, the developed up embryos to the blastocyst stage and the embryos whose growth stopped at the morula stage were collected from women aged 20-30 years old (young group, 94 embryos) and >37 years (old group, 89 embryos). Expression of OCT4, SOX2, CDX2, GATA3, YAP genes and the relevant proteins, in the both groups were evaluated using respectively quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunofluorescence methods. RESULTS: There was no significant difference in the expression level of OCT4, SOX2, CDX2, GATA3 and YAP genes in blastocyst and morula stages, between the two groups. However, SOX2 and CDX2 gene expressions in morula stage embryos of the old group was statistically lower than that of the young group (P=0.007 and P=0.008, respectively). Additionally, in the embryos collected from women with >37 years of age, at the blastocyst stage, phospho-YAP (p-YAP) protein was found to be accumulated in the TE, but it was almost disappeared from the ICM. Additionally, in the old group, contrary to the expectation, YAP protein was expressed in the ICM, rather than TE. CONCLUSION: The results of this study showed that YAP and P-YAP among the Hippo signalling pathway may be altered by increasing age.
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spelling pubmed-74818942020-09-21 Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos Gharanfoli, Sahar Shahverdi, Abdolhossein Dalman, Azam Ghaznavi, Pooneh Alipour, Hiva Eftekhari-Yazdi, Poopak Cell J Original Article OBJECTIVE: The Hippo pathway plays an important role in embryo development, and separation of trophectoderm (TE) and inner cell mass (ICM) cell lines. Therefore, this study investigated effect of maternal age on activity of Hippo pathway in human embryos. MATERIALS AND METHODS: In this experimental study, the developed up embryos to the blastocyst stage and the embryos whose growth stopped at the morula stage were collected from women aged 20-30 years old (young group, 94 embryos) and >37 years (old group, 89 embryos). Expression of OCT4, SOX2, CDX2, GATA3, YAP genes and the relevant proteins, in the both groups were evaluated using respectively quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and immunofluorescence methods. RESULTS: There was no significant difference in the expression level of OCT4, SOX2, CDX2, GATA3 and YAP genes in blastocyst and morula stages, between the two groups. However, SOX2 and CDX2 gene expressions in morula stage embryos of the old group was statistically lower than that of the young group (P=0.007 and P=0.008, respectively). Additionally, in the embryos collected from women with >37 years of age, at the blastocyst stage, phospho-YAP (p-YAP) protein was found to be accumulated in the TE, but it was almost disappeared from the ICM. Additionally, in the old group, contrary to the expectation, YAP protein was expressed in the ICM, rather than TE. CONCLUSION: The results of this study showed that YAP and P-YAP among the Hippo signalling pathway may be altered by increasing age. Royan Institute 2020 2020-09-08 /pmc/articles/PMC7481894/ /pubmed/32779436 http://dx.doi.org/10.22074/cellj.2020.6860 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gharanfoli, Sahar
Shahverdi, Abdolhossein
Dalman, Azam
Ghaznavi, Pooneh
Alipour, Hiva
Eftekhari-Yazdi, Poopak
Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title_full Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title_fullStr Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title_full_unstemmed Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title_short Effect of Maternal Age on Hippo Pathway Related Gene Expressions and Protein Localization Pattern in Human Embryos
title_sort effect of maternal age on hippo pathway related gene expressions and protein localization pattern in human embryos
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481894/
https://www.ncbi.nlm.nih.gov/pubmed/32779436
http://dx.doi.org/10.22074/cellj.2020.6860
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