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Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats

Although aging is associated with a higher risk of developing respiratory pathologies, very few studies have assessed the impact of age on the adverse effects of inhaled nanoparticles. Using conventional and transcriptomic approaches, this study aimed to compare in young (12–13-week-old) and elderly...

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Autores principales: Valentino, Sarah A., Chézeau, Laëtitia, Seidel, Carole, Sébillaud, Sylvie, Lorcin, Mylène, Chalansonnet, Monique, Cosnier, Frédéric, Gaté, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230065/
https://www.ncbi.nlm.nih.gov/pubmed/34206090
http://dx.doi.org/10.3390/nano11061466
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author Valentino, Sarah A.
Chézeau, Laëtitia
Seidel, Carole
Sébillaud, Sylvie
Lorcin, Mylène
Chalansonnet, Monique
Cosnier, Frédéric
Gaté, Laurent
author_facet Valentino, Sarah A.
Chézeau, Laëtitia
Seidel, Carole
Sébillaud, Sylvie
Lorcin, Mylène
Chalansonnet, Monique
Cosnier, Frédéric
Gaté, Laurent
author_sort Valentino, Sarah A.
collection PubMed
description Although aging is associated with a higher risk of developing respiratory pathologies, very few studies have assessed the impact of age on the adverse effects of inhaled nanoparticles. Using conventional and transcriptomic approaches, this study aimed to compare in young (12–13-week-old) and elderly (19-month-old) fisher F344 rats the pulmonary toxicity of an inhaled nanostructured aerosol of titanium dioxide (TiO(2)). Animals were nose-only exposed to this aerosol at a concentration of 10 mg/m(3) for 6 h per day, 5 days per week for 4 weeks. Tissues were collected immediately (D0), and 28 days after exposure (D28). A pulmonary influx of neutrophilic granulocytes was observed in exposed rats at D0, but diminished with time while remaining significant until D28. Similarly, an increased expression of several genes involved in inflammation at the two post-exposure time-points was seen. Apart from an age-specific pulmonary influx of lymphocyte, only slight differences in physio-pathological responses following TiO(2) exposure between young and elderly animals were noticed. Conversely, marked age-related differences in gene expression profiles were observed making possible to establish lists of genes specific to each age group and post-exposure times. These results highlight different signaling pathways that were disrupted in rats according to their age.
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spelling pubmed-82300652021-06-26 Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats Valentino, Sarah A. Chézeau, Laëtitia Seidel, Carole Sébillaud, Sylvie Lorcin, Mylène Chalansonnet, Monique Cosnier, Frédéric Gaté, Laurent Nanomaterials (Basel) Article Although aging is associated with a higher risk of developing respiratory pathologies, very few studies have assessed the impact of age on the adverse effects of inhaled nanoparticles. Using conventional and transcriptomic approaches, this study aimed to compare in young (12–13-week-old) and elderly (19-month-old) fisher F344 rats the pulmonary toxicity of an inhaled nanostructured aerosol of titanium dioxide (TiO(2)). Animals were nose-only exposed to this aerosol at a concentration of 10 mg/m(3) for 6 h per day, 5 days per week for 4 weeks. Tissues were collected immediately (D0), and 28 days after exposure (D28). A pulmonary influx of neutrophilic granulocytes was observed in exposed rats at D0, but diminished with time while remaining significant until D28. Similarly, an increased expression of several genes involved in inflammation at the two post-exposure time-points was seen. Apart from an age-specific pulmonary influx of lymphocyte, only slight differences in physio-pathological responses following TiO(2) exposure between young and elderly animals were noticed. Conversely, marked age-related differences in gene expression profiles were observed making possible to establish lists of genes specific to each age group and post-exposure times. These results highlight different signaling pathways that were disrupted in rats according to their age. MDPI 2021-06-01 /pmc/articles/PMC8230065/ /pubmed/34206090 http://dx.doi.org/10.3390/nano11061466 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Valentino, Sarah A.
Chézeau, Laëtitia
Seidel, Carole
Sébillaud, Sylvie
Lorcin, Mylène
Chalansonnet, Monique
Cosnier, Frédéric
Gaté, Laurent
Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title_full Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title_fullStr Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title_full_unstemmed Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title_short Exposure to TiO(2) Nanostructured Aerosol Induces Specific Gene Expression Profile Modifications in the Lungs of Young and Elderly Rats
title_sort exposure to tio(2) nanostructured aerosol induces specific gene expression profile modifications in the lungs of young and elderly rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230065/
https://www.ncbi.nlm.nih.gov/pubmed/34206090
http://dx.doi.org/10.3390/nano11061466
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