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Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation

This study characterised the changes in global gene expression in the lung of ICR mice in response to the inflammation and fibrosis induced by the inhalation of 0.5 μm polystyrene (PS)-nanoplastics (NPs) at various concentrations (4, 8, and 16 μg/mL) for 2 weeks. The total RNA extracted from the lun...

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Autores principales: Jin, You Jeong, Kim, Ji Eun, Roh, Yu Jeong, Song, Hee Jin, Seol, Ayun, Park, Jumin, Lim, Yong, Seo, Sungbaek, Hwang, Dae Youn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201517/
https://www.ncbi.nlm.nih.gov/pubmed/37360972
http://dx.doi.org/10.1007/s43188-023-00188-y
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author Jin, You Jeong
Kim, Ji Eun
Roh, Yu Jeong
Song, Hee Jin
Seol, Ayun
Park, Jumin
Lim, Yong
Seo, Sungbaek
Hwang, Dae Youn
author_facet Jin, You Jeong
Kim, Ji Eun
Roh, Yu Jeong
Song, Hee Jin
Seol, Ayun
Park, Jumin
Lim, Yong
Seo, Sungbaek
Hwang, Dae Youn
author_sort Jin, You Jeong
collection PubMed
description This study characterised the changes in global gene expression in the lung of ICR mice in response to the inflammation and fibrosis induced by the inhalation of 0.5 μm polystyrene (PS)-nanoplastics (NPs) at various concentrations (4, 8, and 16 μg/mL) for 2 weeks. The total RNA extracted from the lung tissue of NPs-inhaled mice was hybridised into oligonucleotide microarrays. Significant upregulation was detected in several inflammatory responses, including the number of immune cells in bronchoalveolar lavage fluid (BALF), the expression level of inflammatory cytokines, mucin secretion, and histopathological changes, while they accumulated average of 13.38 ± 1.0 μg/g in the lungs of the inhaled ICR mice. Similar responses were observed regarding the levels of fibrosis-related factors in the NPs-inhaled lung of ICR mice, such as pulmonary parenchymal area, expression of pro-fibrotic marker genes, and TGF-β1 downstream signalling without any significant hepatotoxicity and nephrotoxicity. In microarray analyses, 60 genes were upregulated, and 55 genes were downregulated in the lung of ICR mice during inflammation and fibrosis induced by NPs inhalation compared to the Vehicle-inhaled mice. Among these genes, many were categorised into several ontology categories, including the anatomical structure, binding, membrane, and metabolic process. Furthermore, the major genes in the upregulated categories included Igkv14-126000, Egr1, Scel, Lamb3, and Upk3b. In contrast, the major genes in the down-regulated categories were Olfr417, Olfr519, Rps16, Rap2b, and Vmn1r193. These results suggest several gene functional groups and individual genes as specific biomarkers respond to inflammation and fibrosis induced by PS-NPs inhalation in ICR mice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43188-023-00188-y.
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spelling pubmed-102015172023-05-23 Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation Jin, You Jeong Kim, Ji Eun Roh, Yu Jeong Song, Hee Jin Seol, Ayun Park, Jumin Lim, Yong Seo, Sungbaek Hwang, Dae Youn Toxicol Res Original Article This study characterised the changes in global gene expression in the lung of ICR mice in response to the inflammation and fibrosis induced by the inhalation of 0.5 μm polystyrene (PS)-nanoplastics (NPs) at various concentrations (4, 8, and 16 μg/mL) for 2 weeks. The total RNA extracted from the lung tissue of NPs-inhaled mice was hybridised into oligonucleotide microarrays. Significant upregulation was detected in several inflammatory responses, including the number of immune cells in bronchoalveolar lavage fluid (BALF), the expression level of inflammatory cytokines, mucin secretion, and histopathological changes, while they accumulated average of 13.38 ± 1.0 μg/g in the lungs of the inhaled ICR mice. Similar responses were observed regarding the levels of fibrosis-related factors in the NPs-inhaled lung of ICR mice, such as pulmonary parenchymal area, expression of pro-fibrotic marker genes, and TGF-β1 downstream signalling without any significant hepatotoxicity and nephrotoxicity. In microarray analyses, 60 genes were upregulated, and 55 genes were downregulated in the lung of ICR mice during inflammation and fibrosis induced by NPs inhalation compared to the Vehicle-inhaled mice. Among these genes, many were categorised into several ontology categories, including the anatomical structure, binding, membrane, and metabolic process. Furthermore, the major genes in the upregulated categories included Igkv14-126000, Egr1, Scel, Lamb3, and Upk3b. In contrast, the major genes in the down-regulated categories were Olfr417, Olfr519, Rps16, Rap2b, and Vmn1r193. These results suggest several gene functional groups and individual genes as specific biomarkers respond to inflammation and fibrosis induced by PS-NPs inhalation in ICR mice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43188-023-00188-y. Springer Nature Singapore 2023-05-22 /pmc/articles/PMC10201517/ /pubmed/37360972 http://dx.doi.org/10.1007/s43188-023-00188-y Text en © The Author(s) under exclusive licence to Korean Society of Toxicology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
spellingShingle Original Article
Jin, You Jeong
Kim, Ji Eun
Roh, Yu Jeong
Song, Hee Jin
Seol, Ayun
Park, Jumin
Lim, Yong
Seo, Sungbaek
Hwang, Dae Youn
Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title_full Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title_fullStr Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title_full_unstemmed Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title_short Characterisation of changes in global genes expression in the lung of ICR mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
title_sort characterisation of changes in global genes expression in the lung of icr mice in response to the inflammation and fibrosis induced by polystyrene nanoplastics inhalation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201517/
https://www.ncbi.nlm.nih.gov/pubmed/37360972
http://dx.doi.org/10.1007/s43188-023-00188-y
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