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Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows
Liver and mammary gland are among the most important organs during lactation in dairy cows. With the purpose of understanding both the different and the complementary roles and the crosstalk of those two organs during lactation, a transcriptome analysis was performed on liver and mammary tissues of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349457/ https://www.ncbi.nlm.nih.gov/pubmed/28291785 http://dx.doi.org/10.1371/journal.pone.0173082 |
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author | Bu, Dengpan Bionaz, Massimo Wang, Mengzhi Nan, Xuemei Ma, Lu Wang, Jiaqi |
author_facet | Bu, Dengpan Bionaz, Massimo Wang, Mengzhi Nan, Xuemei Ma, Lu Wang, Jiaqi |
author_sort | Bu, Dengpan |
collection | PubMed |
description | Liver and mammary gland are among the most important organs during lactation in dairy cows. With the purpose of understanding both the different and the complementary roles and the crosstalk of those two organs during lactation, a transcriptome analysis was performed on liver and mammary tissues of 10 primiparous dairy cows in mid-lactation. The analysis was performed using a 4×44K Bovine Agilent microarray chip. The transcriptome difference between the two tissues was analyzed using SAS JMP Genomics using ANOVA with a false discovery rate correction (FDR). The analysis uncovered >9,000 genes differentially expressed (DEG) between the two tissues with a FDR<0.001. The functional analysis of the DEG uncovered a larger metabolic (especially related to lipid) and inflammatory response capacity in liver compared with mammary tissue while the mammary tissue had a larger protein synthesis and secretion, proliferation/differentiation, signaling, and innate immune system capacity compared with the liver. A plethora of endogenous compounds, cytokines, and transcription factors were estimated to control the DEG between the two tissues. Compared with mammary tissue, the liver transcriptome appeared to be under control of a large array of ligand-dependent nuclear receptors and, among endogenous chemical, fatty acids and bacteria-derived compounds. Compared with liver, the transcriptome of the mammary tissue was potentially under control of a large number of growth factors and miRNA. The in silico crosstalk analysis between the two tissues revealed an overall large communication with a reciprocal control of lipid metabolism, innate immune system adaptation, and proliferation/differentiation. In summary the transcriptome analysis confirmed prior known differences between liver and mammary tissue, especially considering the indication of a larger metabolic activity in liver compared with the mammary tissue and the larger protein synthesis, communication, and proliferative capacity in mammary tissue compared with the liver. Relatively novel is the indication by the data that the transcriptome of the liver is highly regulated by dietary and bacteria-related compounds while the mammary transcriptome is more under control of hormones, growth factors, and miRNA. A large crosstalk between the two tissues with a reciprocal control of metabolism and innate immune-adaptation was indicated by the network analysis that allowed uncovering previously unknown crosstalk between liver and mammary tissue for several signaling molecules. |
format | Online Article Text |
id | pubmed-5349457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53494572017-04-06 Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows Bu, Dengpan Bionaz, Massimo Wang, Mengzhi Nan, Xuemei Ma, Lu Wang, Jiaqi PLoS One Research Article Liver and mammary gland are among the most important organs during lactation in dairy cows. With the purpose of understanding both the different and the complementary roles and the crosstalk of those two organs during lactation, a transcriptome analysis was performed on liver and mammary tissues of 10 primiparous dairy cows in mid-lactation. The analysis was performed using a 4×44K Bovine Agilent microarray chip. The transcriptome difference between the two tissues was analyzed using SAS JMP Genomics using ANOVA with a false discovery rate correction (FDR). The analysis uncovered >9,000 genes differentially expressed (DEG) between the two tissues with a FDR<0.001. The functional analysis of the DEG uncovered a larger metabolic (especially related to lipid) and inflammatory response capacity in liver compared with mammary tissue while the mammary tissue had a larger protein synthesis and secretion, proliferation/differentiation, signaling, and innate immune system capacity compared with the liver. A plethora of endogenous compounds, cytokines, and transcription factors were estimated to control the DEG between the two tissues. Compared with mammary tissue, the liver transcriptome appeared to be under control of a large array of ligand-dependent nuclear receptors and, among endogenous chemical, fatty acids and bacteria-derived compounds. Compared with liver, the transcriptome of the mammary tissue was potentially under control of a large number of growth factors and miRNA. The in silico crosstalk analysis between the two tissues revealed an overall large communication with a reciprocal control of lipid metabolism, innate immune system adaptation, and proliferation/differentiation. In summary the transcriptome analysis confirmed prior known differences between liver and mammary tissue, especially considering the indication of a larger metabolic activity in liver compared with the mammary tissue and the larger protein synthesis, communication, and proliferative capacity in mammary tissue compared with the liver. Relatively novel is the indication by the data that the transcriptome of the liver is highly regulated by dietary and bacteria-related compounds while the mammary transcriptome is more under control of hormones, growth factors, and miRNA. A large crosstalk between the two tissues with a reciprocal control of metabolism and innate immune-adaptation was indicated by the network analysis that allowed uncovering previously unknown crosstalk between liver and mammary tissue for several signaling molecules. Public Library of Science 2017-03-14 /pmc/articles/PMC5349457/ /pubmed/28291785 http://dx.doi.org/10.1371/journal.pone.0173082 Text en © 2017 Bu 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Bu, Dengpan Bionaz, Massimo Wang, Mengzhi Nan, Xuemei Ma, Lu Wang, Jiaqi Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title | Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title_full | Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title_fullStr | Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title_full_unstemmed | Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title_short | Transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
title_sort | transcriptome difference and potential crosstalk between liver and mammary tissue in mid-lactation primiparous dairy cows |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349457/ https://www.ncbi.nlm.nih.gov/pubmed/28291785 http://dx.doi.org/10.1371/journal.pone.0173082 |
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