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Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions
SCOPE: During pregnancy, mother‐to‐fetus transfer of nutrients is mediated by the placenta; sub‐optimal placental development and/or function results in fetal growth restriction (FGR), and the attendant risk of stillbirth, neurodevelopmental delay, and non‐communicable diseases in adulthood. A mater...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787345/ https://www.ncbi.nlm.nih.gov/pubmed/35938208 http://dx.doi.org/10.1002/mnfr.202200013 |
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author | Timms, Kate Holder, Beth Day, Anil Mclaughlin, John Forbes, Karen A. Westwood, Melissa |
author_facet | Timms, Kate Holder, Beth Day, Anil Mclaughlin, John Forbes, Karen A. Westwood, Melissa |
author_sort | Timms, Kate |
collection | PubMed |
description | SCOPE: During pregnancy, mother‐to‐fetus transfer of nutrients is mediated by the placenta; sub‐optimal placental development and/or function results in fetal growth restriction (FGR), and the attendant risk of stillbirth, neurodevelopmental delay, and non‐communicable diseases in adulthood. A maternal diet high in fruit and vegetables lowers the risk of FGR but the association cannot be explained fully by known macro‐ and micronutrients. METHODS AND RESULTS: This study investigates if dietary‐derived extracellular vesicles (EVs) can regulate placental function. The study characterizes the microRNA and protein cargo of EVs isolated from watermelon, show they are actively internalized by human intestinal epithelial cells in vitro, use mass spectrometry to demonstrate that they alter the intestinal secretome and bioinformatic analyses to predict the likely affected pathways in cells/tissues distal to gut. Application of the watermelon EV‐modified intestinal secretome to human placental trophoblast cells and ex vivo tissue explants affects the trophoblast proteome and key aspects of trophoblast behavior, including migration and syncytialization. CONCLUSION: Dietary‐derived plant EVs can modify intestinal communication with distal tissues, including the placenta. Harnessing the beneficial properties of dietary‐derived plant EVs and/or exploiting their potential as natural delivery agents may provide new ways to improve placental function and reduce rates of FGR. |
format | Online Article Text |
id | pubmed-9787345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97873452022-12-27 Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions Timms, Kate Holder, Beth Day, Anil Mclaughlin, John Forbes, Karen A. Westwood, Melissa Mol Nutr Food Res Research Articles SCOPE: During pregnancy, mother‐to‐fetus transfer of nutrients is mediated by the placenta; sub‐optimal placental development and/or function results in fetal growth restriction (FGR), and the attendant risk of stillbirth, neurodevelopmental delay, and non‐communicable diseases in adulthood. A maternal diet high in fruit and vegetables lowers the risk of FGR but the association cannot be explained fully by known macro‐ and micronutrients. METHODS AND RESULTS: This study investigates if dietary‐derived extracellular vesicles (EVs) can regulate placental function. The study characterizes the microRNA and protein cargo of EVs isolated from watermelon, show they are actively internalized by human intestinal epithelial cells in vitro, use mass spectrometry to demonstrate that they alter the intestinal secretome and bioinformatic analyses to predict the likely affected pathways in cells/tissues distal to gut. Application of the watermelon EV‐modified intestinal secretome to human placental trophoblast cells and ex vivo tissue explants affects the trophoblast proteome and key aspects of trophoblast behavior, including migration and syncytialization. CONCLUSION: Dietary‐derived plant EVs can modify intestinal communication with distal tissues, including the placenta. Harnessing the beneficial properties of dietary‐derived plant EVs and/or exploiting their potential as natural delivery agents may provide new ways to improve placental function and reduce rates of FGR. John Wiley and Sons Inc. 2022-08-19 2022-10 /pmc/articles/PMC9787345/ /pubmed/35938208 http://dx.doi.org/10.1002/mnfr.202200013 Text en © 2022 The Authors. Molecular Nutrition & Food Research published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Timms, Kate Holder, Beth Day, Anil Mclaughlin, John Forbes, Karen A. Westwood, Melissa Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title | Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title_full | Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title_fullStr | Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title_full_unstemmed | Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title_short | Watermelon‐Derived Extracellular Vesicles Influence Human Ex Vivo Placental Cell Behavior by Altering Intestinal Secretions |
title_sort | watermelon‐derived extracellular vesicles influence human ex vivo placental cell behavior by altering intestinal secretions |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787345/ https://www.ncbi.nlm.nih.gov/pubmed/35938208 http://dx.doi.org/10.1002/mnfr.202200013 |
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