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Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat

Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood. This study aimed to investigate the direct effect of PQ on NSC in vivo and its possible mechanism. Adult C57BL/6 mice were subcutaneously injected with 2 mg/kg PQ, 20 mg...

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Autores principales: Yang, Zhengli, Shao, Yiming, Zhao, Yifan, Li, Qian, Li, Rui, Xiao, Hongxi, Zhang, Fen, Zhang, Yilan, Chang, Xiuli, Zhang, Yubin, Zhou, Zhijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576831/
https://www.ncbi.nlm.nih.gov/pubmed/33082501
http://dx.doi.org/10.1038/s41598-020-74916-x
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author Yang, Zhengli
Shao, Yiming
Zhao, Yifan
Li, Qian
Li, Rui
Xiao, Hongxi
Zhang, Fen
Zhang, Yilan
Chang, Xiuli
Zhang, Yubin
Zhou, Zhijun
author_facet Yang, Zhengli
Shao, Yiming
Zhao, Yifan
Li, Qian
Li, Rui
Xiao, Hongxi
Zhang, Fen
Zhang, Yilan
Chang, Xiuli
Zhang, Yubin
Zhou, Zhijun
author_sort Yang, Zhengli
collection PubMed
description Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood. This study aimed to investigate the direct effect of PQ on NSC in vivo and its possible mechanism. Adult C57BL/6 mice were subcutaneously injected with 2 mg/kg PQ, 20 mg/kg PQ or vehicle control once a week for 2 weeks, and sacrificed 1 week after the last PQ injection. Furthermore, extra experiments with Tauroursodeoxycholic Acid (TUDCA) intervention were performed to observe the relationship between ER stress, neuroinflammation and the neural stem cell (NSC) impairment. The results showed that 20 mg/kg PQ caused the NSC number decrease in both subgranular zones (SGZ) and subventricular zone (SVZ). Further analysis indicated that the 20 mg/kg PQ suppressed the proliferation of NSC, without affecting the apoptosis. Moreover, 20 mg/kg PQ also induced ER stress in microglia and caused neuroinflammation in SGZ and SVZ. Interestingly, the ER stress inhibitor could simultaneously ameliorate the neuroinflammation and NSC reduction. These data suggested that increased ER stress in microglia might be a possible pathway for PQ-induced neuroinflammation and NSC impairment. That is a previously unknown mechanism for PQ neurotoxicity.
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spelling pubmed-75768312020-10-23 Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat Yang, Zhengli Shao, Yiming Zhao, Yifan Li, Qian Li, Rui Xiao, Hongxi Zhang, Fen Zhang, Yilan Chang, Xiuli Zhang, Yubin Zhou, Zhijun Sci Rep Article Paraquat (PQ), a widely used herbicide, could cause neurodegenerative diseases, yet the mechanism remains incompletely understood. This study aimed to investigate the direct effect of PQ on NSC in vivo and its possible mechanism. Adult C57BL/6 mice were subcutaneously injected with 2 mg/kg PQ, 20 mg/kg PQ or vehicle control once a week for 2 weeks, and sacrificed 1 week after the last PQ injection. Furthermore, extra experiments with Tauroursodeoxycholic Acid (TUDCA) intervention were performed to observe the relationship between ER stress, neuroinflammation and the neural stem cell (NSC) impairment. The results showed that 20 mg/kg PQ caused the NSC number decrease in both subgranular zones (SGZ) and subventricular zone (SVZ). Further analysis indicated that the 20 mg/kg PQ suppressed the proliferation of NSC, without affecting the apoptosis. Moreover, 20 mg/kg PQ also induced ER stress in microglia and caused neuroinflammation in SGZ and SVZ. Interestingly, the ER stress inhibitor could simultaneously ameliorate the neuroinflammation and NSC reduction. These data suggested that increased ER stress in microglia might be a possible pathway for PQ-induced neuroinflammation and NSC impairment. That is a previously unknown mechanism for PQ neurotoxicity. Nature Publishing Group UK 2020-10-20 /pmc/articles/PMC7576831/ /pubmed/33082501 http://dx.doi.org/10.1038/s41598-020-74916-x Text en © The Author(s) 2020 Open Access This 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/.
spellingShingle Article
Yang, Zhengli
Shao, Yiming
Zhao, Yifan
Li, Qian
Li, Rui
Xiao, Hongxi
Zhang, Fen
Zhang, Yilan
Chang, Xiuli
Zhang, Yubin
Zhou, Zhijun
Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title_full Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title_fullStr Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title_full_unstemmed Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title_short Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
title_sort endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576831/
https://www.ncbi.nlm.nih.gov/pubmed/33082501
http://dx.doi.org/10.1038/s41598-020-74916-x
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