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Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model
(1) Background: The gastrointestinal tract (GI) tract is one of the main organs exposed to particulate matter (PM) directly through ingestion of contaminated food or indirectly through inhalation. Previous studies have investigated the effects of chronic PM exposure on intestinal epithelia in vitro...
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/PMC7246573/ https://www.ncbi.nlm.nih.gov/pubmed/32384765 http://dx.doi.org/10.3390/ijerph17093234 |
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author | Woodby, Brittany Schiavone, Maria Lucia Pambianchi, Erika Mastaloudis, Angela N. Hester, Shelly M. Wood, Steven Pecorelli, Alessandra Valacchi, Giuseppe |
author_facet | Woodby, Brittany Schiavone, Maria Lucia Pambianchi, Erika Mastaloudis, Angela N. Hester, Shelly M. Wood, Steven Pecorelli, Alessandra Valacchi, Giuseppe |
author_sort | Woodby, Brittany |
collection | PubMed |
description | (1) Background: The gastrointestinal tract (GI) tract is one of the main organs exposed to particulate matter (PM) directly through ingestion of contaminated food or indirectly through inhalation. Previous studies have investigated the effects of chronic PM exposure on intestinal epithelia in vitro using Caco−2 cells and in vivo using mice. In this study, we hypothesized that chronic PM exposure would increase epithelial permeability and decrease barrier function due to altered redox homeostasis, which alters levels and/or localization of barrier-associated proteins in human three-dimensional (3D) intestinal tissues. (2) Methods: Transepithelial electrical resistance (TEER) in tissues exposed to 50, 100, 150, 250, and 500 µg/cm(2) of PM for 1 week and 2 weeks was analyzed. Levels and localization of tight junction proteins zonula occludens protein 1 (ZO−1) and claudin−1 and desmosome-associated desmocollin were analyzed using immunofluorescence. As a marker of oxidative stress, levels of 4-hydroxy-nonenal (4HNE) adducts were measured. (3) Results: No differences in TEER measurements were observed between exposed and un-exposed tissues. However, increased levels of 4HNE adducts in exposed tissues were observed. Additionally, decreased levels of ZO−1, claudin−1, and desmocollin were demonstrated. (4) Conclusion: These data suggest that chronic PM exposure results in an increase of oxidative stress; modified levels of barrier-associated proteins could possibly link to GI tract inflammatory conditions. |
format | Online Article Text |
id | pubmed-7246573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72465732020-06-10 Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model Woodby, Brittany Schiavone, Maria Lucia Pambianchi, Erika Mastaloudis, Angela N. Hester, Shelly M. Wood, Steven Pecorelli, Alessandra Valacchi, Giuseppe Int J Environ Res Public Health Article (1) Background: The gastrointestinal tract (GI) tract is one of the main organs exposed to particulate matter (PM) directly through ingestion of contaminated food or indirectly through inhalation. Previous studies have investigated the effects of chronic PM exposure on intestinal epithelia in vitro using Caco−2 cells and in vivo using mice. In this study, we hypothesized that chronic PM exposure would increase epithelial permeability and decrease barrier function due to altered redox homeostasis, which alters levels and/or localization of barrier-associated proteins in human three-dimensional (3D) intestinal tissues. (2) Methods: Transepithelial electrical resistance (TEER) in tissues exposed to 50, 100, 150, 250, and 500 µg/cm(2) of PM for 1 week and 2 weeks was analyzed. Levels and localization of tight junction proteins zonula occludens protein 1 (ZO−1) and claudin−1 and desmosome-associated desmocollin were analyzed using immunofluorescence. As a marker of oxidative stress, levels of 4-hydroxy-nonenal (4HNE) adducts were measured. (3) Results: No differences in TEER measurements were observed between exposed and un-exposed tissues. However, increased levels of 4HNE adducts in exposed tissues were observed. Additionally, decreased levels of ZO−1, claudin−1, and desmocollin were demonstrated. (4) Conclusion: These data suggest that chronic PM exposure results in an increase of oxidative stress; modified levels of barrier-associated proteins could possibly link to GI tract inflammatory conditions. MDPI 2020-05-06 2020-05 /pmc/articles/PMC7246573/ /pubmed/32384765 http://dx.doi.org/10.3390/ijerph17093234 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 Woodby, Brittany Schiavone, Maria Lucia Pambianchi, Erika Mastaloudis, Angela N. Hester, Shelly M. Wood, Steven Pecorelli, Alessandra Valacchi, Giuseppe Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title | Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title_full | Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title_fullStr | Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title_full_unstemmed | Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title_short | Particulate Matter Decreases Intestinal Barrier-Associated Proteins Levels in 3D Human Intestinal Model |
title_sort | particulate matter decreases intestinal barrier-associated proteins levels in 3d human intestinal model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246573/ https://www.ncbi.nlm.nih.gov/pubmed/32384765 http://dx.doi.org/10.3390/ijerph17093234 |
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