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Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study
Human milk (HM) is a complex biofluid containing a wide cell variety including epithelial cells and leukocytes. However, the cellular compositions and their phenotypic properties over the course of lactation are poorly understood. The aim of this preliminary study was to characterize the cellular me...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10005050/ https://www.ncbi.nlm.nih.gov/pubmed/36904100 http://dx.doi.org/10.3390/nu15051100 |
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author | Ten-Doménech, Isabel Cascant-Vilaplana, Mari Merce Navarro-Esteve, Víctor Felderer, Birgit Moreno-Giménez, Alba Rienda, Iván Gormaz, María Moreno-Torres, Marta Pérez-Guaita, David Quintás, Guillermo Kuligowski, Julia |
author_facet | Ten-Doménech, Isabel Cascant-Vilaplana, Mari Merce Navarro-Esteve, Víctor Felderer, Birgit Moreno-Giménez, Alba Rienda, Iván Gormaz, María Moreno-Torres, Marta Pérez-Guaita, David Quintás, Guillermo Kuligowski, Julia |
author_sort | Ten-Doménech, Isabel |
collection | PubMed |
description | Human milk (HM) is a complex biofluid containing a wide cell variety including epithelial cells and leukocytes. However, the cellular compositions and their phenotypic properties over the course of lactation are poorly understood. The aim of this preliminary study was to characterize the cellular metabolome of HM over the course of lactation. Cells were isolated via centrifugation and the cellular fraction was characterized via cytomorphology and immunocytochemical staining. Cell metabolites were extracted and analyzed using ultra-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UPLC–QqTOF-MS) in the positive and negative electrospray ionization modes. Immunocytochemical analysis revealed a high variability of the number of detected cells with relative median abundances of 98% of glandular epithelial cells, 1% of leukocytes, and 1% of keratinocytes. Significant correlations between the milk postnatal age with percentage of epithelial cells and leukocytes, and with total cell count were observed. Results from the Hierarchical Cluster Analysis of immunocytochemical profiles were very similar to those observed in the analysis of the metabolomic profiles. In addition, metabolic pathway analysis showed alterations in seven metabolic pathways correlating with postnatal age. This work paves the way for future investigations on changes in the metabolomic fraction of the cellular compartment of HM. |
format | Online Article Text |
id | pubmed-10005050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100050502023-03-11 Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study Ten-Doménech, Isabel Cascant-Vilaplana, Mari Merce Navarro-Esteve, Víctor Felderer, Birgit Moreno-Giménez, Alba Rienda, Iván Gormaz, María Moreno-Torres, Marta Pérez-Guaita, David Quintás, Guillermo Kuligowski, Julia Nutrients Article Human milk (HM) is a complex biofluid containing a wide cell variety including epithelial cells and leukocytes. However, the cellular compositions and their phenotypic properties over the course of lactation are poorly understood. The aim of this preliminary study was to characterize the cellular metabolome of HM over the course of lactation. Cells were isolated via centrifugation and the cellular fraction was characterized via cytomorphology and immunocytochemical staining. Cell metabolites were extracted and analyzed using ultra-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UPLC–QqTOF-MS) in the positive and negative electrospray ionization modes. Immunocytochemical analysis revealed a high variability of the number of detected cells with relative median abundances of 98% of glandular epithelial cells, 1% of leukocytes, and 1% of keratinocytes. Significant correlations between the milk postnatal age with percentage of epithelial cells and leukocytes, and with total cell count were observed. Results from the Hierarchical Cluster Analysis of immunocytochemical profiles were very similar to those observed in the analysis of the metabolomic profiles. In addition, metabolic pathway analysis showed alterations in seven metabolic pathways correlating with postnatal age. This work paves the way for future investigations on changes in the metabolomic fraction of the cellular compartment of HM. MDPI 2023-02-22 /pmc/articles/PMC10005050/ /pubmed/36904100 http://dx.doi.org/10.3390/nu15051100 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ten-Doménech, Isabel Cascant-Vilaplana, Mari Merce Navarro-Esteve, Víctor Felderer, Birgit Moreno-Giménez, Alba Rienda, Iván Gormaz, María Moreno-Torres, Marta Pérez-Guaita, David Quintás, Guillermo Kuligowski, Julia Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title | Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title_full | Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title_fullStr | Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title_full_unstemmed | Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title_short | Metabolomic Diversity of Human Milk Cells over the Course of Lactation—A Preliminary Study |
title_sort | metabolomic diversity of human milk cells over the course of lactation—a preliminary study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10005050/ https://www.ncbi.nlm.nih.gov/pubmed/36904100 http://dx.doi.org/10.3390/nu15051100 |
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