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MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro

Previous work from our laboratory demonstrated the existence of miRNAs in human follicular fluid. In the current study, we have sought to identify miRNAs that might affect oocyte/embryo quality in patients undergoing intracytoplasmic sperm injection and to investigate their roles in in vitro fertili...

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Autores principales: Feng, Ruizhi, Sang, Qing, Zhu, Yan, Fu, Wei, Liu, Miao, Xu, Yan, Shi, Huijuan, Xu, Yao, Qu, Ronggui, Chai, Renjie, Shao, Ruijin, Jin, Li, He, Lin, Sun, Xiaoxi, Wang, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346788/
https://www.ncbi.nlm.nih.gov/pubmed/25732513
http://dx.doi.org/10.1038/srep08689
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author Feng, Ruizhi
Sang, Qing
Zhu, Yan
Fu, Wei
Liu, Miao
Xu, Yan
Shi, Huijuan
Xu, Yao
Qu, Ronggui
Chai, Renjie
Shao, Ruijin
Jin, Li
He, Lin
Sun, Xiaoxi
Wang, Lei
author_facet Feng, Ruizhi
Sang, Qing
Zhu, Yan
Fu, Wei
Liu, Miao
Xu, Yan
Shi, Huijuan
Xu, Yao
Qu, Ronggui
Chai, Renjie
Shao, Ruijin
Jin, Li
He, Lin
Sun, Xiaoxi
Wang, Lei
author_sort Feng, Ruizhi
collection PubMed
description Previous work from our laboratory demonstrated the existence of miRNAs in human follicular fluid. In the current study, we have sought to identify miRNAs that might affect oocyte/embryo quality in patients undergoing intracytoplasmic sperm injection and to investigate their roles in in vitro fertilization outcomes in mouse oocytes. 53 samples were classified as Group 1 (high quality) if the day-3 embryos had seven and more cells or as Group 2 (low quality) if the embryos had six and fewer cells. TaqMan Human microRNAs cards and qRT-PCR were performed to verify differently expressed miRNAs. The function of the corresponding miRNA was investigated in mouse oocytes by injecting them with miRNA-inhibitor oligonucleotides. We found that hsa-miR-320a and hsa-miR-197 had significantly higher expression levels in the Group 1 follicular fluids than in Group 2 (p = 0.0073 and p = 0.008, respectively). Knockdown of mmu-miR-320 in mouse oocytes strongly decreased the proportions of MII oocytes that developed into two-cell and blastocyst stage embryos (p = 0.0048 and p = 0.0069, respectively). Wnt signaling pathway components had abnormal expression level in miR-320 inhibitor-injected oocytes. This study provides the first evidence that miRNAs in human follicular fluid are indicative of and can influence embryo quality.
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spelling pubmed-43467882015-04-06 MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro Feng, Ruizhi Sang, Qing Zhu, Yan Fu, Wei Liu, Miao Xu, Yan Shi, Huijuan Xu, Yao Qu, Ronggui Chai, Renjie Shao, Ruijin Jin, Li He, Lin Sun, Xiaoxi Wang, Lei Sci Rep Article Previous work from our laboratory demonstrated the existence of miRNAs in human follicular fluid. In the current study, we have sought to identify miRNAs that might affect oocyte/embryo quality in patients undergoing intracytoplasmic sperm injection and to investigate their roles in in vitro fertilization outcomes in mouse oocytes. 53 samples were classified as Group 1 (high quality) if the day-3 embryos had seven and more cells or as Group 2 (low quality) if the embryos had six and fewer cells. TaqMan Human microRNAs cards and qRT-PCR were performed to verify differently expressed miRNAs. The function of the corresponding miRNA was investigated in mouse oocytes by injecting them with miRNA-inhibitor oligonucleotides. We found that hsa-miR-320a and hsa-miR-197 had significantly higher expression levels in the Group 1 follicular fluids than in Group 2 (p = 0.0073 and p = 0.008, respectively). Knockdown of mmu-miR-320 in mouse oocytes strongly decreased the proportions of MII oocytes that developed into two-cell and blastocyst stage embryos (p = 0.0048 and p = 0.0069, respectively). Wnt signaling pathway components had abnormal expression level in miR-320 inhibitor-injected oocytes. This study provides the first evidence that miRNAs in human follicular fluid are indicative of and can influence embryo quality. Nature Publishing Group 2015-03-03 /pmc/articles/PMC4346788/ /pubmed/25732513 http://dx.doi.org/10.1038/srep08689 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Feng, Ruizhi
Sang, Qing
Zhu, Yan
Fu, Wei
Liu, Miao
Xu, Yan
Shi, Huijuan
Xu, Yao
Qu, Ronggui
Chai, Renjie
Shao, Ruijin
Jin, Li
He, Lin
Sun, Xiaoxi
Wang, Lei
MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title_full MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title_fullStr MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title_full_unstemmed MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title_short MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
title_sort mirna-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4346788/
https://www.ncbi.nlm.nih.gov/pubmed/25732513
http://dx.doi.org/10.1038/srep08689
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