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Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk
Human milk (HM) contains regulatory biomolecules including miRNAs, the origin and functional significance of which are still undetermined. We used TaqMan OpenArrays to profile 681 mature miRNAs in HM cells and fat, and compared them with maternal peripheral blood mononuclear cells (PBMCs) and plasma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745068/ https://www.ncbi.nlm.nih.gov/pubmed/26854194 http://dx.doi.org/10.1038/srep20680 |
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author | Alsaweed, Mohammed Lai, Ching Tat Hartmann, Peter E. Geddes, Donna T. Kakulas, Foteini |
author_facet | Alsaweed, Mohammed Lai, Ching Tat Hartmann, Peter E. Geddes, Donna T. Kakulas, Foteini |
author_sort | Alsaweed, Mohammed |
collection | PubMed |
description | Human milk (HM) contains regulatory biomolecules including miRNAs, the origin and functional significance of which are still undetermined. We used TaqMan OpenArrays to profile 681 mature miRNAs in HM cells and fat, and compared them with maternal peripheral blood mononuclear cells (PBMCs) and plasma, and bovine and soy infant formulae. HM cells and PBMCs (292 and 345 miRNAs, respectively) had higher miRNA content than HM fat and plasma (242 and 219 miRNAs, respectively) (p < 0.05). A strong association in miRNA profiles was found between HM cells and fat, whilst PBMCs and plasma were distinctly different to HM, displaying marked inter-individual variation. Considering the dominance of epithelial cells in mature milk of healthy women, these results suggest that HM miRNAs primarily originate from the mammary epithelium, whilst the maternal circulation may have a smaller contribution. Our findings demonstrate that unlike infant formulae, which contained very few human miRNA, HM is a rich source of lactation-specific miRNA, which could be used as biomarkers of the performance and health status of the lactating mammary gland. Given the recently identified stability, uptake and functionality of food- and milk-derived miRNA in vivo, HM miRNA are likely to contribute to infant protection and development. |
format | Online Article Text |
id | pubmed-4745068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47450682016-02-16 Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk Alsaweed, Mohammed Lai, Ching Tat Hartmann, Peter E. Geddes, Donna T. Kakulas, Foteini Sci Rep Article Human milk (HM) contains regulatory biomolecules including miRNAs, the origin and functional significance of which are still undetermined. We used TaqMan OpenArrays to profile 681 mature miRNAs in HM cells and fat, and compared them with maternal peripheral blood mononuclear cells (PBMCs) and plasma, and bovine and soy infant formulae. HM cells and PBMCs (292 and 345 miRNAs, respectively) had higher miRNA content than HM fat and plasma (242 and 219 miRNAs, respectively) (p < 0.05). A strong association in miRNA profiles was found between HM cells and fat, whilst PBMCs and plasma were distinctly different to HM, displaying marked inter-individual variation. Considering the dominance of epithelial cells in mature milk of healthy women, these results suggest that HM miRNAs primarily originate from the mammary epithelium, whilst the maternal circulation may have a smaller contribution. Our findings demonstrate that unlike infant formulae, which contained very few human miRNA, HM is a rich source of lactation-specific miRNA, which could be used as biomarkers of the performance and health status of the lactating mammary gland. Given the recently identified stability, uptake and functionality of food- and milk-derived miRNA in vivo, HM miRNA are likely to contribute to infant protection and development. Nature Publishing Group 2016-02-08 /pmc/articles/PMC4745068/ /pubmed/26854194 http://dx.doi.org/10.1038/srep20680 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Alsaweed, Mohammed Lai, Ching Tat Hartmann, Peter E. Geddes, Donna T. Kakulas, Foteini Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title | Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title_full | Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title_fullStr | Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title_full_unstemmed | Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title_short | Human milk miRNAs primarily originate from the mammary gland resulting in unique miRNA profiles of fractionated milk |
title_sort | human milk mirnas primarily originate from the mammary gland resulting in unique mirna profiles of fractionated milk |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745068/ https://www.ncbi.nlm.nih.gov/pubmed/26854194 http://dx.doi.org/10.1038/srep20680 |
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