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Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro

The aim of this study was to investigate the effect and mechanism of bone morphogenetic protein-6 (BMP-6) on the growth and maturation of mouse follicles in vitro. Preantral follicles isolated from mice were incubated with recombinant human BMP-6 (rhBMP-6) before analysis. BMP-6 expression was detec...

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Autores principales: Wang, Xiyan, Su, Li, Pan, Xiaoyan, Yao, Jian, Li, Zhixin, Wang, Xuenan, Xu, Bangsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434072/
https://www.ncbi.nlm.nih.gov/pubmed/26019649
http://dx.doi.org/10.1080/13102818.2014.996605
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author Wang, Xiyan
Su, Li
Pan, Xiaoyan
Yao, Jian
Li, Zhixin
Wang, Xuenan
Xu, Bangsheng
author_facet Wang, Xiyan
Su, Li
Pan, Xiaoyan
Yao, Jian
Li, Zhixin
Wang, Xuenan
Xu, Bangsheng
author_sort Wang, Xiyan
collection PubMed
description The aim of this study was to investigate the effect and mechanism of bone morphogenetic protein-6 (BMP-6) on the growth and maturation of mouse follicles in vitro. Preantral follicles isolated from mice were incubated with recombinant human BMP-6 (rhBMP-6) before analysis. BMP-6 expression was detected by immunofluorescence and western blot. Maturation of oocytes was observed microscopically. Estradiol (E(2)) and progesterone (P(4)) levels were measured by enzyme-linked immunosorbent assay. Expression of steroidogenesis-related genes was detected by reverse transcription quantitative polymerase chain reaction. There was a marked increase in the preantral follicles maturation in cells incubated with 50 ng/mL of rhBMP-6 for eight days, compared with the control. The levels of E(2), P(4) and steroidogenesis-related genes were also significantly increased in granulosa cells and theca cells cultured for 6, 10 and 11 days, respectively. Conversely, the preantral follicle maturing rate was remarkably decreased in cells incubated with 50 ng/mL of rhBMP-6 for day 11, accompanied with reduction in E(2), P(4) levels and steroidogenesis-related genes levels. Meanwhile, compared with the control, the maturing rate was not significantly different in cells incubated with 100 ng/mL of rhBMP-6 for day 8 or day 11. However, the E(2) levels and its relevant regulation gene expression all increased significantly, while the P(4) content and its relevant regulation gene expression decreased. The results indicate that BMP-6 can promote the maturation of preantral follicles in vitro in a concentration and time-dependent manner and may play a role in the regulation of steroid hormone synthesis and/or secretion.
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spelling pubmed-44340722015-05-25 Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro Wang, Xiyan Su, Li Pan, Xiaoyan Yao, Jian Li, Zhixin Wang, Xuenan Xu, Bangsheng Biotechnol Biotechnol Equip Articles; Medical Biotechnology The aim of this study was to investigate the effect and mechanism of bone morphogenetic protein-6 (BMP-6) on the growth and maturation of mouse follicles in vitro. Preantral follicles isolated from mice were incubated with recombinant human BMP-6 (rhBMP-6) before analysis. BMP-6 expression was detected by immunofluorescence and western blot. Maturation of oocytes was observed microscopically. Estradiol (E(2)) and progesterone (P(4)) levels were measured by enzyme-linked immunosorbent assay. Expression of steroidogenesis-related genes was detected by reverse transcription quantitative polymerase chain reaction. There was a marked increase in the preantral follicles maturation in cells incubated with 50 ng/mL of rhBMP-6 for eight days, compared with the control. The levels of E(2), P(4) and steroidogenesis-related genes were also significantly increased in granulosa cells and theca cells cultured for 6, 10 and 11 days, respectively. Conversely, the preantral follicle maturing rate was remarkably decreased in cells incubated with 50 ng/mL of rhBMP-6 for day 11, accompanied with reduction in E(2), P(4) levels and steroidogenesis-related genes levels. Meanwhile, compared with the control, the maturing rate was not significantly different in cells incubated with 100 ng/mL of rhBMP-6 for day 8 or day 11. However, the E(2) levels and its relevant regulation gene expression all increased significantly, while the P(4) content and its relevant regulation gene expression decreased. The results indicate that BMP-6 can promote the maturation of preantral follicles in vitro in a concentration and time-dependent manner and may play a role in the regulation of steroid hormone synthesis and/or secretion. Taylor & Francis 2015-03-04 2015-01-14 /pmc/articles/PMC4434072/ /pubmed/26019649 http://dx.doi.org/10.1080/13102818.2014.996605 Text en © 2015 The Author(s). Published by Taylor & Francis. 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 work is properly cited.
spellingShingle Articles; Medical Biotechnology
Wang, Xiyan
Su, Li
Pan, Xiaoyan
Yao, Jian
Li, Zhixin
Wang, Xuenan
Xu, Bangsheng
Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title_full Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title_fullStr Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title_full_unstemmed Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title_short Effect of BMP-6 on development and maturation of mouse preantral follicles in vitro
title_sort effect of bmp-6 on development and maturation of mouse preantral follicles in vitro
topic Articles; Medical Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434072/
https://www.ncbi.nlm.nih.gov/pubmed/26019649
http://dx.doi.org/10.1080/13102818.2014.996605
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