Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics

Polystyrene (PS) nanoplastic exposure has been shown to affect the viability of neuronal cells isolated from mouse embryonic brains. However, the viability of mouse embryonic fibroblasts (MEFs) was not affected although PS nanoplastics accumulated in the cytoplasm. It is currently unknown whether ME...

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Main Authors: Seung-Woo Han, Jinhee Choi, Kwon-Yul Ryu
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/4/2094
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spelling doaj-2128e77b7450463d973a0d19eaa91d872021-02-21T00:01:13ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-02-01222094209410.3390/ijms22042094Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene NanoplasticsSeung-Woo Han0Jinhee Choi1Kwon-Yul Ryu2Department of Life Science, University of Seoul, Seoul 02504, KoreaSchool of Environmental Engineering, University of Seoul, Seoul 02504, KoreaDepartment of Life Science, University of Seoul, Seoul 02504, KoreaPolystyrene (PS) nanoplastic exposure has been shown to affect the viability of neuronal cells isolated from mouse embryonic brains. However, the viability of mouse embryonic fibroblasts (MEFs) was not affected although PS nanoplastics accumulated in the cytoplasm. It is currently unknown whether MEFs do not respond to PS nanoplastics or their cellular functions are altered without compromising viability. Here, we found that PS nanoplastics entered the cells via endocytosis and were then released into the cytoplasm, probably by endosomal escape, or otherwise remained in the endosome. Oxidative and inflammatory stress caused by intracellular PS nanoplastics induced the antioxidant response pathway and activated the autophagic pathway. However, colocalization of the autophagic marker LC3B and PS nanoplastics suggested that PS nanoplastics in the cytoplasm might interfere with normal autophagic function. Furthermore, autophagic flux could be impaired, probably due to accumulation of PS nanoplastic-containing lysosomes or autolysosomes. Intriguingly, the level of accumulated PS nanoplastics decreased during prolonged culture when MEFs were no longer exposed to PS nanoplastics. These results indicate that accumulated PS nanoplastics are removed or exported out of the cells. Therefore, PS nanoplastics in the cytoplasm affect cellular functions, but it is temporal and MEFs can overcome the stress caused by PS nanoplastic exposure.https://www.mdpi.com/1422-0067/22/4/2094nanoplasticpolystyreneMEFsendocytosisoxidative stressautophagy
collection DOAJ
language English
format Article
sources DOAJ
author Seung-Woo Han
Jinhee Choi
Kwon-Yul Ryu
spellingShingle Seung-Woo Han
Jinhee Choi
Kwon-Yul Ryu
Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
International Journal of Molecular Sciences
nanoplastic
polystyrene
MEFs
endocytosis
oxidative stress
autophagy
author_facet Seung-Woo Han
Jinhee Choi
Kwon-Yul Ryu
author_sort Seung-Woo Han
title Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
title_short Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
title_full Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
title_fullStr Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
title_full_unstemmed Stress Response of Mouse Embryonic Fibroblasts Exposed to Polystyrene Nanoplastics
title_sort stress response of mouse embryonic fibroblasts exposed to polystyrene nanoplastics
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-02-01
description Polystyrene (PS) nanoplastic exposure has been shown to affect the viability of neuronal cells isolated from mouse embryonic brains. However, the viability of mouse embryonic fibroblasts (MEFs) was not affected although PS nanoplastics accumulated in the cytoplasm. It is currently unknown whether MEFs do not respond to PS nanoplastics or their cellular functions are altered without compromising viability. Here, we found that PS nanoplastics entered the cells via endocytosis and were then released into the cytoplasm, probably by endosomal escape, or otherwise remained in the endosome. Oxidative and inflammatory stress caused by intracellular PS nanoplastics induced the antioxidant response pathway and activated the autophagic pathway. However, colocalization of the autophagic marker LC3B and PS nanoplastics suggested that PS nanoplastics in the cytoplasm might interfere with normal autophagic function. Furthermore, autophagic flux could be impaired, probably due to accumulation of PS nanoplastic-containing lysosomes or autolysosomes. Intriguingly, the level of accumulated PS nanoplastics decreased during prolonged culture when MEFs were no longer exposed to PS nanoplastics. These results indicate that accumulated PS nanoplastics are removed or exported out of the cells. Therefore, PS nanoplastics in the cytoplasm affect cellular functions, but it is temporal and MEFs can overcome the stress caused by PS nanoplastic exposure.
topic nanoplastic
polystyrene
MEFs
endocytosis
oxidative stress
autophagy
url https://www.mdpi.com/1422-0067/22/4/2094
work_keys_str_mv AT seungwoohan stressresponseofmouseembryonicfibroblastsexposedtopolystyrenenanoplastics
AT jinheechoi stressresponseofmouseembryonicfibroblastsexposedtopolystyrenenanoplastics
AT kwonyulryu stressresponseofmouseembryonicfibroblastsexposedtopolystyrenenanoplastics
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