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Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine

Chronic inflammatory conditions can negatively impact intestinal barrier function and affect the epithelium's interaction with nano-sized materials. We demonstrate the application of a Caco-2/THP-1 co-culture mimicking the intestine in healthy (i.e. stable) or inflamed state in nanotoxicologica...

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Autores principales: Kämpfer, Angela A.M., Urbán, Patricia, La Spina, Rita, Jiménez, Isaac Ojea, Kanase, Nilesh, Stone, Vicki, Kinsner-Ovaskainen, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961208/
https://www.ncbi.nlm.nih.gov/pubmed/31760064
http://dx.doi.org/10.1016/j.tiv.2019.104738
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author Kämpfer, Angela A.M.
Urbán, Patricia
La Spina, Rita
Jiménez, Isaac Ojea
Kanase, Nilesh
Stone, Vicki
Kinsner-Ovaskainen, Agnieszka
author_facet Kämpfer, Angela A.M.
Urbán, Patricia
La Spina, Rita
Jiménez, Isaac Ojea
Kanase, Nilesh
Stone, Vicki
Kinsner-Ovaskainen, Agnieszka
author_sort Kämpfer, Angela A.M.
collection PubMed
description Chronic inflammatory conditions can negatively impact intestinal barrier function and affect the epithelium's interaction with nano-sized materials. We demonstrate the application of a Caco-2/THP-1 co-culture mimicking the intestine in healthy (i.e. stable) or inflamed state in nanotoxicological research. The co-cultures were exposed to non-toxic concentrations of silver nanoparticles (AgNPs) or silver nitrate (AgNO(3)) for 24 h. The barrier integrity and cytokine release as well as necrotic and apoptotic cell death were investigated. AgNPs and AgNO(3) most strongly affected the inflamed co-culture. Higher concentrations of AgNPs induced a significant increase in barrier integrity in the inflamed but not the stable co-culture. Necrotic and apoptotic cell death was detected in both conditions but were significantly more pronounced in the inflamed condition. The exposure to AgNO(3) affected barrier integrity in all experimental set-ups, but caused nuclear condensation only in the Caco-2 monoculture and the inflamed co-culture. AgNPs reduced the release of monocyte chemoattractant protein-1 in the stable model. Clear differences were observed in the effects of AgNPs and AgNO(3) in relation to the model's health status. The results suggest an increased vulnerability of the inflamed epithelial barrier towards AgNPs underlining the importance to consider the intestinal health status in the safety assessment of nanomaterials.
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spelling pubmed-69612082020-03-01 Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine Kämpfer, Angela A.M. Urbán, Patricia La Spina, Rita Jiménez, Isaac Ojea Kanase, Nilesh Stone, Vicki Kinsner-Ovaskainen, Agnieszka Toxicol In Vitro Article Chronic inflammatory conditions can negatively impact intestinal barrier function and affect the epithelium's interaction with nano-sized materials. We demonstrate the application of a Caco-2/THP-1 co-culture mimicking the intestine in healthy (i.e. stable) or inflamed state in nanotoxicological research. The co-cultures were exposed to non-toxic concentrations of silver nanoparticles (AgNPs) or silver nitrate (AgNO(3)) for 24 h. The barrier integrity and cytokine release as well as necrotic and apoptotic cell death were investigated. AgNPs and AgNO(3) most strongly affected the inflamed co-culture. Higher concentrations of AgNPs induced a significant increase in barrier integrity in the inflamed but not the stable co-culture. Necrotic and apoptotic cell death was detected in both conditions but were significantly more pronounced in the inflamed condition. The exposure to AgNO(3) affected barrier integrity in all experimental set-ups, but caused nuclear condensation only in the Caco-2 monoculture and the inflamed co-culture. AgNPs reduced the release of monocyte chemoattractant protein-1 in the stable model. Clear differences were observed in the effects of AgNPs and AgNO(3) in relation to the model's health status. The results suggest an increased vulnerability of the inflamed epithelial barrier towards AgNPs underlining the importance to consider the intestinal health status in the safety assessment of nanomaterials. Pergamon Press 2020-03 /pmc/articles/PMC6961208/ /pubmed/31760064 http://dx.doi.org/10.1016/j.tiv.2019.104738 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kämpfer, Angela A.M.
Urbán, Patricia
La Spina, Rita
Jiménez, Isaac Ojea
Kanase, Nilesh
Stone, Vicki
Kinsner-Ovaskainen, Agnieszka
Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title_full Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title_fullStr Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title_full_unstemmed Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title_short Ongoing inflammation enhances the toxicity of engineered nanomaterials: Application of an in vitro co-culture model of the healthy and inflamed intestine
title_sort ongoing inflammation enhances the toxicity of engineered nanomaterials: application of an in vitro co-culture model of the healthy and inflamed intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961208/
https://www.ncbi.nlm.nih.gov/pubmed/31760064
http://dx.doi.org/10.1016/j.tiv.2019.104738
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