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The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells

The aim of this study was to determine the molecular mechanism of miR-205b targeting 11β-hydroxysteroid dehydrogenase type 1 (HSD11B1) on the apoptosis and proliferation of granulosa cells (GC) of pigeons. Our previous studies suggested that HSD11B1 was the target gene of miR-205b and played a key r...

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Autores principales: Wang, Ying, Yang, Hai-ming, Zi, Chen, Gu, Jing, Wang, Zhiyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647703/
https://www.ncbi.nlm.nih.gov/pubmed/33142527
http://dx.doi.org/10.1016/j.psj.2020.06.048
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author Wang, Ying
Yang, Hai-ming
Zi, Chen
Gu, Jing
Wang, Zhiyue
author_facet Wang, Ying
Yang, Hai-ming
Zi, Chen
Gu, Jing
Wang, Zhiyue
author_sort Wang, Ying
collection PubMed
description The aim of this study was to determine the molecular mechanism of miR-205b targeting 11β-hydroxysteroid dehydrogenase type 1 (HSD11B1) on the apoptosis and proliferation of granulosa cells (GC) of pigeons. Our previous studies suggested that HSD11B1 was the target gene of miR-205b and played a key role in steroid hormone biosynthesis and GC development. The adenovirus-miR-205b recombinant virus and adenovirus-cli-miR-205b-sh recombinant virus were generated, verified, and their characteristics determined. The recombinant viruses were used to infect the GC of pigeons, with real time quantitative PCR used to examine the expressions of HSD11B1 and related genes. The HSD11B1 antibody was obtained and verified, and Western blotting was used to detect the protein level of HSD11B1. The Cell Counting Kit–8 assay kit was used to detect cell viability, and the Annexin V-FITC/PI kit was used for the apoptosis assays. The expression of HSD11B1 was significantly lower in the overexpression (OE) than in OE negative control (OE-NC) treatments and significantly higher in short hairpin (SH) than in SH negative control (SH-NC) treatments. The expression levels of cytochrome P4503A5 was significantly higher in SH and lower in OE treatments, and the rhythms of cytochrome P450 aromatase mRNA levels were similar. The mRNA level of cytochrome P450scc in OE was lower than in OE-NC treatments and higher in SH than in SH-NC treatments. The protein expressions of HSD11B1 were decreased in the GC of OE, whereas increased in the SH group. The Cell Counting Kit–8 assay revealed that overexpression of miR-205b significantly suppressed proliferation of the GC of pigeons, whereas interference of miR-205b significantly induced the proliferation of the GC. The overexpression and the interference of miR-205b did not have a significant effect on cell cycle. The overexpression of miR-205b significantly increased the number of apoptotic cells, whereas the interference of miR-205b decreased the number of apoptotic cells. These findings indicated that miR-205b mediated pigeon egg production by regulating the steroid hormone biosynthesis of the pigeon ovarian GC by targeting HSD11B1, which may be useful in increasing pigeon egg production.
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spelling pubmed-76477032020-11-13 The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells Wang, Ying Yang, Hai-ming Zi, Chen Gu, Jing Wang, Zhiyue Poult Sci Physiology and Reproduction The aim of this study was to determine the molecular mechanism of miR-205b targeting 11β-hydroxysteroid dehydrogenase type 1 (HSD11B1) on the apoptosis and proliferation of granulosa cells (GC) of pigeons. Our previous studies suggested that HSD11B1 was the target gene of miR-205b and played a key role in steroid hormone biosynthesis and GC development. The adenovirus-miR-205b recombinant virus and adenovirus-cli-miR-205b-sh recombinant virus were generated, verified, and their characteristics determined. The recombinant viruses were used to infect the GC of pigeons, with real time quantitative PCR used to examine the expressions of HSD11B1 and related genes. The HSD11B1 antibody was obtained and verified, and Western blotting was used to detect the protein level of HSD11B1. The Cell Counting Kit–8 assay kit was used to detect cell viability, and the Annexin V-FITC/PI kit was used for the apoptosis assays. The expression of HSD11B1 was significantly lower in the overexpression (OE) than in OE negative control (OE-NC) treatments and significantly higher in short hairpin (SH) than in SH negative control (SH-NC) treatments. The expression levels of cytochrome P4503A5 was significantly higher in SH and lower in OE treatments, and the rhythms of cytochrome P450 aromatase mRNA levels were similar. The mRNA level of cytochrome P450scc in OE was lower than in OE-NC treatments and higher in SH than in SH-NC treatments. The protein expressions of HSD11B1 were decreased in the GC of OE, whereas increased in the SH group. The Cell Counting Kit–8 assay revealed that overexpression of miR-205b significantly suppressed proliferation of the GC of pigeons, whereas interference of miR-205b significantly induced the proliferation of the GC. The overexpression and the interference of miR-205b did not have a significant effect on cell cycle. The overexpression of miR-205b significantly increased the number of apoptotic cells, whereas the interference of miR-205b decreased the number of apoptotic cells. These findings indicated that miR-205b mediated pigeon egg production by regulating the steroid hormone biosynthesis of the pigeon ovarian GC by targeting HSD11B1, which may be useful in increasing pigeon egg production. Elsevier 2020-07-08 /pmc/articles/PMC7647703/ /pubmed/33142527 http://dx.doi.org/10.1016/j.psj.2020.06.048 Text en © 2020 Published by Elsevier Inc. on behalf of Poultry Science Association Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Physiology and Reproduction
Wang, Ying
Yang, Hai-ming
Zi, Chen
Gu, Jing
Wang, Zhiyue
The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title_full The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title_fullStr The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title_full_unstemmed The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title_short The mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
title_sort mediation of pigeon egg production by regulating the steroid hormone biosynthesis of pigeon ovarian granulosa cells
topic Physiology and Reproduction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647703/
https://www.ncbi.nlm.nih.gov/pubmed/33142527
http://dx.doi.org/10.1016/j.psj.2020.06.048
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