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Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro
Palmitic acid (PA), a long-chain saturated fatty acid, might activate innate immune cells. PA plays a role in chronic liver disease, diabetes and Crohn’s disease, all of which are associated with impaired intestinal permeability. We investigated the effect of PA, at physiological postprandial intest...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278681/ https://www.ncbi.nlm.nih.gov/pubmed/32414055 http://dx.doi.org/10.3390/antiox9050417 |
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author | Gori, Manuele Altomare, Annamaria Cocca, Silvia Solida, Eleonora Ribolsi, Mentore Carotti, Simone Rainer, Alberto Francesconi, Maria Morini, Sergio Cicala, Michele Pier Luca Guarino, Michele |
author_facet | Gori, Manuele Altomare, Annamaria Cocca, Silvia Solida, Eleonora Ribolsi, Mentore Carotti, Simone Rainer, Alberto Francesconi, Maria Morini, Sergio Cicala, Michele Pier Luca Guarino, Michele |
author_sort | Gori, Manuele |
collection | PubMed |
description | Palmitic acid (PA), a long-chain saturated fatty acid, might activate innate immune cells. PA plays a role in chronic liver disease, diabetes and Crohn’s disease, all of which are associated with impaired intestinal permeability. We investigated the effect of PA, at physiological postprandial intestinal concentrations, on gut epithelium as compared to lipopolysaccharide (LPS) and ethanol, using an in vitro gut model, the human intestinal epithelial cell line Caco-2 grown on transwell inserts. Cytotoxicity and oxidative stress were evaluated; epithelial barrier integrity was investigated by measuring the paracellular flux of fluorescein, and through RT-qPCR and immunofluorescence of tight junction (TJ) and adherens junction (AJ) mRNAs and proteins, respectively. In PA-exposed Caco-2 monolayers, cytotoxicity and oxidative stress were not detected. A significant increase in fluorescein flux was observed in PA-treated monolayers, after 90 min and up to 360 min, whereas with LPS and ethanol, this was only observed at later time-points. Gene expression and immunofluorescence analysis showed TJ and AJ alterations only in PA-exposed monolayers. In conclusion, PA affected intestinal permeability without inducing cytotoxicity or oxidative stress. This effect seemed to be faster and stronger than those with LPS and ethanol. Thus, we hypothesized that PA, besides having an immunomodulatory effect, might play a role in inflammatory and functional intestinal disorders in which the intestinal permeability is altered. |
format | Online Article Text |
id | pubmed-7278681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72786812020-06-12 Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro Gori, Manuele Altomare, Annamaria Cocca, Silvia Solida, Eleonora Ribolsi, Mentore Carotti, Simone Rainer, Alberto Francesconi, Maria Morini, Sergio Cicala, Michele Pier Luca Guarino, Michele Antioxidants (Basel) Article Palmitic acid (PA), a long-chain saturated fatty acid, might activate innate immune cells. PA plays a role in chronic liver disease, diabetes and Crohn’s disease, all of which are associated with impaired intestinal permeability. We investigated the effect of PA, at physiological postprandial intestinal concentrations, on gut epithelium as compared to lipopolysaccharide (LPS) and ethanol, using an in vitro gut model, the human intestinal epithelial cell line Caco-2 grown on transwell inserts. Cytotoxicity and oxidative stress were evaluated; epithelial barrier integrity was investigated by measuring the paracellular flux of fluorescein, and through RT-qPCR and immunofluorescence of tight junction (TJ) and adherens junction (AJ) mRNAs and proteins, respectively. In PA-exposed Caco-2 monolayers, cytotoxicity and oxidative stress were not detected. A significant increase in fluorescein flux was observed in PA-treated monolayers, after 90 min and up to 360 min, whereas with LPS and ethanol, this was only observed at later time-points. Gene expression and immunofluorescence analysis showed TJ and AJ alterations only in PA-exposed monolayers. In conclusion, PA affected intestinal permeability without inducing cytotoxicity or oxidative stress. This effect seemed to be faster and stronger than those with LPS and ethanol. Thus, we hypothesized that PA, besides having an immunomodulatory effect, might play a role in inflammatory and functional intestinal disorders in which the intestinal permeability is altered. MDPI 2020-05-13 /pmc/articles/PMC7278681/ /pubmed/32414055 http://dx.doi.org/10.3390/antiox9050417 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gori, Manuele Altomare, Annamaria Cocca, Silvia Solida, Eleonora Ribolsi, Mentore Carotti, Simone Rainer, Alberto Francesconi, Maria Morini, Sergio Cicala, Michele Pier Luca Guarino, Michele Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title | Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title_full | Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title_fullStr | Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title_full_unstemmed | Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title_short | Palmitic Acid Affects Intestinal Epithelial Barrier Integrity and Permeability In Vitro |
title_sort | palmitic acid affects intestinal epithelial barrier integrity and permeability in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278681/ https://www.ncbi.nlm.nih.gov/pubmed/32414055 http://dx.doi.org/10.3390/antiox9050417 |
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