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Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid
Pluripotent human amniotic fluid cells (HuAFCs) can differentiate into various types of somatic cell in vitro. However, their differentiation into oocyte-like cells has never been described to the best of our knowledge. In the present study, differentiation of E-cadherin(+) and E-cadherin(−) HuAFC s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4068722/ https://www.ncbi.nlm.nih.gov/pubmed/24788191 http://dx.doi.org/10.3892/mmr.2014.2199 |
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author | LIU, TE HUANG, YONGYI BU, YANZHEN ZHAO, YANHUI ZOU, GANG LIU, ZHIXUE |
author_facet | LIU, TE HUANG, YONGYI BU, YANZHEN ZHAO, YANHUI ZOU, GANG LIU, ZHIXUE |
author_sort | LIU, TE |
collection | PubMed |
description | Pluripotent human amniotic fluid cells (HuAFCs) can differentiate into various types of somatic cell in vitro. However, their differentiation into oocyte-like cells has never been described to the best of our knowledge. In the present study, differentiation of E-cadherin(+) and E-cadherin(−) HuAFC sub-populations into oocyte-like cells was induced via culture in medium containing bovine follicular fluid and β-mercaptoethanol. The E-cadherin(+) HuAFCs expressed DAZL highly. Post-induction, cells with an oocyte-like phenotype were found among the E-cadherin(+) HuAFCs, expressing markers specific to germ cells and oocytes (VASA, ZP3 and GDF9) and meiosis (DMC1 and SCP3). When specific small interfering RNA (siRNA) was used to suppress E-cadherin in the E-cadherin(+) HuAFCs, the levels of DAZL expression were reduced. Post-induction, the morphology of the siRNA-E-cadherin HuAFCs was poorer and the expression levels of germ cell-specific markers were lower compared with those of the siRNA-mock HuAFCs. Therefore, E-cadherin(+) HuAFCs could be more easily induced to differentiate into oocyte-like cells by bovine follicular fluid and β-mercaptoethanol. In addition, the E-cadherin(+) HuAFCs exhibited potential characteristics of DAZL protein expression, and thus it was conjectured that bovine follicular fluid acts on DAZL protein and promotes E-cadherin(+) HuAFC differentiation into oocyte-like cells. |
format | Online Article Text |
id | pubmed-4068722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-40687222014-06-25 Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid LIU, TE HUANG, YONGYI BU, YANZHEN ZHAO, YANHUI ZOU, GANG LIU, ZHIXUE Mol Med Rep Articles Pluripotent human amniotic fluid cells (HuAFCs) can differentiate into various types of somatic cell in vitro. However, their differentiation into oocyte-like cells has never been described to the best of our knowledge. In the present study, differentiation of E-cadherin(+) and E-cadherin(−) HuAFC sub-populations into oocyte-like cells was induced via culture in medium containing bovine follicular fluid and β-mercaptoethanol. The E-cadherin(+) HuAFCs expressed DAZL highly. Post-induction, cells with an oocyte-like phenotype were found among the E-cadherin(+) HuAFCs, expressing markers specific to germ cells and oocytes (VASA, ZP3 and GDF9) and meiosis (DMC1 and SCP3). When specific small interfering RNA (siRNA) was used to suppress E-cadherin in the E-cadherin(+) HuAFCs, the levels of DAZL expression were reduced. Post-induction, the morphology of the siRNA-E-cadherin HuAFCs was poorer and the expression levels of germ cell-specific markers were lower compared with those of the siRNA-mock HuAFCs. Therefore, E-cadherin(+) HuAFCs could be more easily induced to differentiate into oocyte-like cells by bovine follicular fluid and β-mercaptoethanol. In addition, the E-cadherin(+) HuAFCs exhibited potential characteristics of DAZL protein expression, and thus it was conjectured that bovine follicular fluid acts on DAZL protein and promotes E-cadherin(+) HuAFC differentiation into oocyte-like cells. D.A. Spandidos 2014-07 2014-04-29 /pmc/articles/PMC4068722/ /pubmed/24788191 http://dx.doi.org/10.3892/mmr.2014.2199 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles LIU, TE HUANG, YONGYI BU, YANZHEN ZHAO, YANHUI ZOU, GANG LIU, ZHIXUE Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title | Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title_full | Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title_fullStr | Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title_full_unstemmed | Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title_short | Induction of E-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
title_sort | induction of e-cadherin(+) human amniotic fluid cell differentiation into oocyte-like cells via culture in medium supplemented with follicular fluid |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4068722/ https://www.ncbi.nlm.nih.gov/pubmed/24788191 http://dx.doi.org/10.3892/mmr.2014.2199 |
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