Cargando…

Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis

BACKGROUND: Micro- and nanoplastic pollution has become a global environmental problem. Nanoplastics in the environment are still hard to detect because of analysis technology limitations. It is believed that when microplastics are found in the environment, more undetected nanoplastics are around. T...

Descripción completa

Detalles Bibliográficos
Autores principales: Liang, Boxuan, Zhong, Yizhou, Huang, Yuji, Lin, Xi, Liu, Jun, Lin, Li, Hu, Manjiang, Jiang, Junying, Dai, Mingzhu, Wang, Bo, Zhang, Bingli, Meng, Hao, Lelaka, Jesse Justin J., Sui, Haixia, Yang, Xingfen, Huang, Zhenlie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186235/
https://www.ncbi.nlm.nih.gov/pubmed/34098985
http://dx.doi.org/10.1186/s12989-021-00414-1
_version_ 1783704920389582848
author Liang, Boxuan
Zhong, Yizhou
Huang, Yuji
Lin, Xi
Liu, Jun
Lin, Li
Hu, Manjiang
Jiang, Junying
Dai, Mingzhu
Wang, Bo
Zhang, Bingli
Meng, Hao
Lelaka, Jesse Justin J.
Sui, Haixia
Yang, Xingfen
Huang, Zhenlie
author_facet Liang, Boxuan
Zhong, Yizhou
Huang, Yuji
Lin, Xi
Liu, Jun
Lin, Li
Hu, Manjiang
Jiang, Junying
Dai, Mingzhu
Wang, Bo
Zhang, Bingli
Meng, Hao
Lelaka, Jesse Justin J.
Sui, Haixia
Yang, Xingfen
Huang, Zhenlie
author_sort Liang, Boxuan
collection PubMed
description BACKGROUND: Micro- and nanoplastic pollution has become a global environmental problem. Nanoplastics in the environment are still hard to detect because of analysis technology limitations. It is believed that when microplastics are found in the environment, more undetected nanoplastics are around. The current “microplastic exposure” is in fact the mixture of micro- and nanoplastic exposures. Therefore, the biological interaction between organisms among different sizes of micro- and nanoplastics should not be neglected. RESULTS: We measured the biodistribution of three polystyrene (PS) particles (50 nm PS, PS50; 500 nm PS, PS500; 5000 nm PS, PS5000) under single and co-exposure conditions in mice. We explored the underlying mechanisms by investigating the effects on three major components of the intestinal barrier (the mucus layer, tight junctions and the epithelial cells) in four intestine segments (duodenum, jejunum, ileum and colon) of mice. We found that the amounts of both PS500 and PS5000 increased when they were co-exposed with PS50 for 24 h in the mice. These increased amounts were due primarily to the increased permeability in the mouse intestines. We also confirmed there was a combined toxicity of PS50 and PS500 in the mouse intestines. This manifested as the mixture of PS50 and PS500 causing more severe dysfunction of the intestinal barrier than that caused by PS50 or PS500 alone. We found that the combined toxicity of PS micro- and nanoplastics on intestinal barrier dysfunction was caused primarily by reactive oxygen species (ROS)-mediated epithelial cell apoptosis in the mice. These findings were further confirmed by an oxidants or antioxidants pretreatment study. In addition, the combined toxicity of PS micro- and nanoplastics was also found in the mice after a 28-day repeated dose exposure. CONCLUSIONS: There is a combined toxicity of PS50 and PS500 in the mouse intestines, which was caused primarily by ROS-mediated epithelial cell apoptosis in the mice. Considering that most recent studies on PS micro- and nanoplastics have been conducted using a single particle size, the health risks of exposure to PS micro- and nanoplastics on organisms may be underestimated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12989-021-00414-1.
format Online
Article
Text
id pubmed-8186235
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81862352021-06-10 Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis Liang, Boxuan Zhong, Yizhou Huang, Yuji Lin, Xi Liu, Jun Lin, Li Hu, Manjiang Jiang, Junying Dai, Mingzhu Wang, Bo Zhang, Bingli Meng, Hao Lelaka, Jesse Justin J. Sui, Haixia Yang, Xingfen Huang, Zhenlie Part Fibre Toxicol Research BACKGROUND: Micro- and nanoplastic pollution has become a global environmental problem. Nanoplastics in the environment are still hard to detect because of analysis technology limitations. It is believed that when microplastics are found in the environment, more undetected nanoplastics are around. The current “microplastic exposure” is in fact the mixture of micro- and nanoplastic exposures. Therefore, the biological interaction between organisms among different sizes of micro- and nanoplastics should not be neglected. RESULTS: We measured the biodistribution of three polystyrene (PS) particles (50 nm PS, PS50; 500 nm PS, PS500; 5000 nm PS, PS5000) under single and co-exposure conditions in mice. We explored the underlying mechanisms by investigating the effects on three major components of the intestinal barrier (the mucus layer, tight junctions and the epithelial cells) in four intestine segments (duodenum, jejunum, ileum and colon) of mice. We found that the amounts of both PS500 and PS5000 increased when they were co-exposed with PS50 for 24 h in the mice. These increased amounts were due primarily to the increased permeability in the mouse intestines. We also confirmed there was a combined toxicity of PS50 and PS500 in the mouse intestines. This manifested as the mixture of PS50 and PS500 causing more severe dysfunction of the intestinal barrier than that caused by PS50 or PS500 alone. We found that the combined toxicity of PS micro- and nanoplastics on intestinal barrier dysfunction was caused primarily by reactive oxygen species (ROS)-mediated epithelial cell apoptosis in the mice. These findings were further confirmed by an oxidants or antioxidants pretreatment study. In addition, the combined toxicity of PS micro- and nanoplastics was also found in the mice after a 28-day repeated dose exposure. CONCLUSIONS: There is a combined toxicity of PS50 and PS500 in the mouse intestines, which was caused primarily by ROS-mediated epithelial cell apoptosis in the mice. Considering that most recent studies on PS micro- and nanoplastics have been conducted using a single particle size, the health risks of exposure to PS micro- and nanoplastics on organisms may be underestimated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12989-021-00414-1. BioMed Central 2021-06-07 /pmc/articles/PMC8186235/ /pubmed/34098985 http://dx.doi.org/10.1186/s12989-021-00414-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liang, Boxuan
Zhong, Yizhou
Huang, Yuji
Lin, Xi
Liu, Jun
Lin, Li
Hu, Manjiang
Jiang, Junying
Dai, Mingzhu
Wang, Bo
Zhang, Bingli
Meng, Hao
Lelaka, Jesse Justin J.
Sui, Haixia
Yang, Xingfen
Huang, Zhenlie
Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title_full Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title_fullStr Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title_full_unstemmed Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title_short Underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ROS-mediated epithelial cell apoptosis
title_sort underestimated health risks: polystyrene micro- and nanoplastics jointly induce intestinal barrier dysfunction by ros-mediated epithelial cell apoptosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186235/
https://www.ncbi.nlm.nih.gov/pubmed/34098985
http://dx.doi.org/10.1186/s12989-021-00414-1
work_keys_str_mv AT liangboxuan underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT zhongyizhou underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT huangyuji underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT linxi underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT liujun underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT linli underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT humanjiang underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT jiangjunying underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT daimingzhu underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT wangbo underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT zhangbingli underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT menghao underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT lelakajessejustinj underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT suihaixia underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT yangxingfen underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis
AT huangzhenlie underestimatedhealthriskspolystyrenemicroandnanoplasticsjointlyinduceintestinalbarrierdysfunctionbyrosmediatedepithelialcellapoptosis