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Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome

Heat shock protein 27 (Hsp27) is a heat shock protein family member which can inhibit apoptosis. Our previous studies reported down-regulated Hsp27 in ovarian tissue derived from women with polycystic ovary syndrome (PCOS) however, the exact effect of Hsp27 on oocyte maturation and developmental com...

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Autores principales: Cai, Lingbo, Ma, Xiang, Liu, Shan, Liu, Jinjuan, Wang, Wei, Cui, Yugui, Ding, Wei, Mao, Yundong, Chen, Huiping, Huang, Jie, Zhou, Zuomin, Liu, Jiayin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877038/
https://www.ncbi.nlm.nih.gov/pubmed/24391762
http://dx.doi.org/10.1371/journal.pone.0083402
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author Cai, Lingbo
Ma, Xiang
Liu, Shan
Liu, Jinjuan
Wang, Wei
Cui, Yugui
Ding, Wei
Mao, Yundong
Chen, Huiping
Huang, Jie
Zhou, Zuomin
Liu, Jiayin
author_facet Cai, Lingbo
Ma, Xiang
Liu, Shan
Liu, Jinjuan
Wang, Wei
Cui, Yugui
Ding, Wei
Mao, Yundong
Chen, Huiping
Huang, Jie
Zhou, Zuomin
Liu, Jiayin
author_sort Cai, Lingbo
collection PubMed
description Heat shock protein 27 (Hsp27) is a heat shock protein family member which can inhibit apoptosis. Our previous studies reported down-regulated Hsp27 in ovarian tissue derived from women with polycystic ovary syndrome (PCOS) however, the exact effect of Hsp27 on oocyte maturation and developmental competence in PCOS is unclear. The effect of Hsp27 over-expression was studied in vitro using oocytes derived from PCOS patients. An artificial GFP-plasmid was injected into human oocyte to increase Hsp27 protein level. Oocyte maturation was evaluated by morphological observation. Mature oocytes were fertilized by intracytoplasmic sperm injection (ICSI) and embryonic developmental competence was evaluated. Critical apoptotic factors and cytokines were measured at both the mRNA and protein level. Our results revealed that Overexpression of HSP27 lowered the maturation rate of oocytes derived from PCOS patients. Meanwhile, fertilization rate and high quality embryo rate were similar between the Hsp27 overexpressing group and controls; however, the blastocyst formation rate in this group was significantly higher than control. Expression analysis revealed that the oocyte-secreted factors, BMP15 and GDF9, and the apoptotic-related regulators, Caspase 3, 8 and 9, were all significantly decreased in Hsp27 overexpressing oocytes. In conclusion, upregulation of Hsp27 inhibits oocyte maturation from PCOS patients, but improves embryonic developmental potential.
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spelling pubmed-38770382014-01-03 Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome Cai, Lingbo Ma, Xiang Liu, Shan Liu, Jinjuan Wang, Wei Cui, Yugui Ding, Wei Mao, Yundong Chen, Huiping Huang, Jie Zhou, Zuomin Liu, Jiayin PLoS One Research Article Heat shock protein 27 (Hsp27) is a heat shock protein family member which can inhibit apoptosis. Our previous studies reported down-regulated Hsp27 in ovarian tissue derived from women with polycystic ovary syndrome (PCOS) however, the exact effect of Hsp27 on oocyte maturation and developmental competence in PCOS is unclear. The effect of Hsp27 over-expression was studied in vitro using oocytes derived from PCOS patients. An artificial GFP-plasmid was injected into human oocyte to increase Hsp27 protein level. Oocyte maturation was evaluated by morphological observation. Mature oocytes were fertilized by intracytoplasmic sperm injection (ICSI) and embryonic developmental competence was evaluated. Critical apoptotic factors and cytokines were measured at both the mRNA and protein level. Our results revealed that Overexpression of HSP27 lowered the maturation rate of oocytes derived from PCOS patients. Meanwhile, fertilization rate and high quality embryo rate were similar between the Hsp27 overexpressing group and controls; however, the blastocyst formation rate in this group was significantly higher than control. Expression analysis revealed that the oocyte-secreted factors, BMP15 and GDF9, and the apoptotic-related regulators, Caspase 3, 8 and 9, were all significantly decreased in Hsp27 overexpressing oocytes. In conclusion, upregulation of Hsp27 inhibits oocyte maturation from PCOS patients, but improves embryonic developmental potential. Public Library of Science 2013-12-31 /pmc/articles/PMC3877038/ /pubmed/24391762 http://dx.doi.org/10.1371/journal.pone.0083402 Text en © 2013 Cai 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cai, Lingbo
Ma, Xiang
Liu, Shan
Liu, Jinjuan
Wang, Wei
Cui, Yugui
Ding, Wei
Mao, Yundong
Chen, Huiping
Huang, Jie
Zhou, Zuomin
Liu, Jiayin
Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title_full Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title_fullStr Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title_full_unstemmed Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title_short Effects of Upregulation of Hsp27 Expression on Oocyte Development and Maturation Derived from Polycystic Ovary Syndrome
title_sort effects of upregulation of hsp27 expression on oocyte development and maturation derived from polycystic ovary syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877038/
https://www.ncbi.nlm.nih.gov/pubmed/24391762
http://dx.doi.org/10.1371/journal.pone.0083402
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