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Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure

Plastics in the environment can break down into nanoplastics (NPs), which pose a potential threat to public health. Studies have shown that the nervous system constitutes a significant target for nanoplastics. However, the potential mechanism behind nanoplastics’ neurotoxicity remains unknown. This...

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Autores principales: Liu, Qingping, Hu, Wentao, Zhang, Yaling, Ning, Jie, Pang, Yaxian, Hu, Huaifang, Chen, Meiyu, Wu, Mengqi, Wang, Mengruo, Yang, Peihao, Bao, Lei, Niu, Yujie, Zhang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386552/
https://www.ncbi.nlm.nih.gov/pubmed/37505566
http://dx.doi.org/10.3390/toxics11070600
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author Liu, Qingping
Hu, Wentao
Zhang, Yaling
Ning, Jie
Pang, Yaxian
Hu, Huaifang
Chen, Meiyu
Wu, Mengqi
Wang, Mengruo
Yang, Peihao
Bao, Lei
Niu, Yujie
Zhang, Rong
author_facet Liu, Qingping
Hu, Wentao
Zhang, Yaling
Ning, Jie
Pang, Yaxian
Hu, Huaifang
Chen, Meiyu
Wu, Mengqi
Wang, Mengruo
Yang, Peihao
Bao, Lei
Niu, Yujie
Zhang, Rong
author_sort Liu, Qingping
collection PubMed
description Plastics in the environment can break down into nanoplastics (NPs), which pose a potential threat to public health. Studies have shown that the nervous system constitutes a significant target for nanoplastics. However, the potential mechanism behind nanoplastics’ neurotoxicity remains unknown. This study aimed to investigate the role of lncRNA in the depressive-like responses induced by exposure to 25 nm polystyrene nanoplastics (PS NPs). Forty mice were divided into four groups administered doses of 0, 10, 25, and 50 mg/kg via gavage for 6 months. After conducting behavioral tests, RNA sequencing was used to detect changes in mRNAs, miRNAs, and lncRNAs in the prefrontal cortex of the mice in the 0 and 50 mg/kg PS NPs groups. The results revealed that mice exposed to chronic PS NPs developed depressive-like responses in a dose-dependent manner. It was demonstrated that 987 mRNAs, 29 miRNAs, and 116 lncRNAs were significantly different between the two groups. Then, a competing endogenous RNA (ceRNA) network containing 6 lncRNAs, 18 miRNAs, and 750 mRNAs was constructed. Enrichment results suggested that PS NPs may contribute to the onset of depression-like responses through the activation of axon guidance, neurotrophin-signaling pathways, and dopaminergic synapses. This study provided evidence of the molecular relationship between PS NPs and depression-like responses.
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spelling pubmed-103865522023-07-30 Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure Liu, Qingping Hu, Wentao Zhang, Yaling Ning, Jie Pang, Yaxian Hu, Huaifang Chen, Meiyu Wu, Mengqi Wang, Mengruo Yang, Peihao Bao, Lei Niu, Yujie Zhang, Rong Toxics Article Plastics in the environment can break down into nanoplastics (NPs), which pose a potential threat to public health. Studies have shown that the nervous system constitutes a significant target for nanoplastics. However, the potential mechanism behind nanoplastics’ neurotoxicity remains unknown. This study aimed to investigate the role of lncRNA in the depressive-like responses induced by exposure to 25 nm polystyrene nanoplastics (PS NPs). Forty mice were divided into four groups administered doses of 0, 10, 25, and 50 mg/kg via gavage for 6 months. After conducting behavioral tests, RNA sequencing was used to detect changes in mRNAs, miRNAs, and lncRNAs in the prefrontal cortex of the mice in the 0 and 50 mg/kg PS NPs groups. The results revealed that mice exposed to chronic PS NPs developed depressive-like responses in a dose-dependent manner. It was demonstrated that 987 mRNAs, 29 miRNAs, and 116 lncRNAs were significantly different between the two groups. Then, a competing endogenous RNA (ceRNA) network containing 6 lncRNAs, 18 miRNAs, and 750 mRNAs was constructed. Enrichment results suggested that PS NPs may contribute to the onset of depression-like responses through the activation of axon guidance, neurotrophin-signaling pathways, and dopaminergic synapses. This study provided evidence of the molecular relationship between PS NPs and depression-like responses. MDPI 2023-07-10 /pmc/articles/PMC10386552/ /pubmed/37505566 http://dx.doi.org/10.3390/toxics11070600 Text en © 2023 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
Liu, Qingping
Hu, Wentao
Zhang, Yaling
Ning, Jie
Pang, Yaxian
Hu, Huaifang
Chen, Meiyu
Wu, Mengqi
Wang, Mengruo
Yang, Peihao
Bao, Lei
Niu, Yujie
Zhang, Rong
Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title_full Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title_fullStr Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title_full_unstemmed Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title_short Comprehensive Analysis of lncRNA–mRNA Expression Profiles in Depression-like Responses of Mice Related to Polystyrene Nanoparticle Exposure
title_sort comprehensive analysis of lncrna–mrna expression profiles in depression-like responses of mice related to polystyrene nanoparticle exposure
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386552/
https://www.ncbi.nlm.nih.gov/pubmed/37505566
http://dx.doi.org/10.3390/toxics11070600
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