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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...

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Autores principales: Timms, Kate, Holder, Beth, Day, Anil, Mclaughlin, John, Forbes, Karen A., Westwood, Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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