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MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells
The MEN1 gene, which encodes the protein Menin, was investigated for its regulatory role in milk protein synthesis in mammary glands. Menin responds to nutrient and hormone levels via the PI3K/Akt/mTOR pathway. Bovine mammary epithelial cells and tissues were used as experimental models in this stud...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511157/ https://www.ncbi.nlm.nih.gov/pubmed/28710500 http://dx.doi.org/10.1038/s41598-017-06054-w |
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author | Li, Honghui Liu, Xue Wang, Zhonghua Lin, Xueyan Yan, Zhengui Cao, Qiaoqiao Zhao, Meng Shi, Kerong |
author_facet | Li, Honghui Liu, Xue Wang, Zhonghua Lin, Xueyan Yan, Zhengui Cao, Qiaoqiao Zhao, Meng Shi, Kerong |
author_sort | Li, Honghui |
collection | PubMed |
description | The MEN1 gene, which encodes the protein Menin, was investigated for its regulatory role in milk protein synthesis in mammary glands. Menin responds to nutrient and hormone levels via the PI3K/Akt/mTOR pathway. Bovine mammary epithelial cells and tissues were used as experimental models in this study. The results revealed that the milk protein synthesis capacity of mammary epithelial cells could be regulated by MEN1/Menin. The overexpression of Menin caused significant suppression of factors involved in the mTOR pathway, as well as milk protein κ-casein (CSNK). In contrast, a significant increase in these factors and CSNK was observed upon MEN1/Menin knockdown. The repression of MEN1/Menin on the mTOR pathway was also observed in mammary gland tissues. Additionally, MEN1/Menin was found to elicit a negative response on prolactin (PRL) and/or insulin (INS), which caused a similar downstream impact on mTOR pathway factors and milk proteins. Collectively, our data indicate that MEN1/Menin could play a regulatory role in milk protein synthesis through mTOR signaling in the mammary gland by mediating the effects of hormones and nutrient status. The discovery of Menin’s role in mammary glands suggests Menin could be potential new target for the improvement of milk performance and adjustment of lactation period of dairy cows. |
format | Online Article Text |
id | pubmed-5511157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55111572017-07-17 MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells Li, Honghui Liu, Xue Wang, Zhonghua Lin, Xueyan Yan, Zhengui Cao, Qiaoqiao Zhao, Meng Shi, Kerong Sci Rep Article The MEN1 gene, which encodes the protein Menin, was investigated for its regulatory role in milk protein synthesis in mammary glands. Menin responds to nutrient and hormone levels via the PI3K/Akt/mTOR pathway. Bovine mammary epithelial cells and tissues were used as experimental models in this study. The results revealed that the milk protein synthesis capacity of mammary epithelial cells could be regulated by MEN1/Menin. The overexpression of Menin caused significant suppression of factors involved in the mTOR pathway, as well as milk protein κ-casein (CSNK). In contrast, a significant increase in these factors and CSNK was observed upon MEN1/Menin knockdown. The repression of MEN1/Menin on the mTOR pathway was also observed in mammary gland tissues. Additionally, MEN1/Menin was found to elicit a negative response on prolactin (PRL) and/or insulin (INS), which caused a similar downstream impact on mTOR pathway factors and milk proteins. Collectively, our data indicate that MEN1/Menin could play a regulatory role in milk protein synthesis through mTOR signaling in the mammary gland by mediating the effects of hormones and nutrient status. The discovery of Menin’s role in mammary glands suggests Menin could be potential new target for the improvement of milk performance and adjustment of lactation period of dairy cows. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511157/ /pubmed/28710500 http://dx.doi.org/10.1038/s41598-017-06054-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Li, Honghui Liu, Xue Wang, Zhonghua Lin, Xueyan Yan, Zhengui Cao, Qiaoqiao Zhao, Meng Shi, Kerong MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title | MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title_full | MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title_fullStr | MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title_full_unstemmed | MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title_short | MEN1/Menin regulates milk protein synthesis through mTOR signaling in mammary epithelial cells |
title_sort | men1/menin regulates milk protein synthesis through mtor signaling in mammary epithelial cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511157/ https://www.ncbi.nlm.nih.gov/pubmed/28710500 http://dx.doi.org/10.1038/s41598-017-06054-w |
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