Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models
The pathological hallmarks of Parkinson's disease (PD) are the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc) and the presence of overactivated glial cells and neuroinflammation. Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) c...
Main Authors: | , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
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Elsevier
2020-02-01
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Series: | Redox Biology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S221323171931184X |
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doaj-5636ed92da3c4549990d28a5025cc45a |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zishan Wang Hongtian Dong Jinghui Wang Yulu Huang Xiaoshuang Zhang Yilin Tang Qing Li Zhaolin Liu Yuanyuan Ma Jiabin Tong Li Huang Jian Fei Mei Yu Jian Wang Fang Huang |
spellingShingle |
Zishan Wang Hongtian Dong Jinghui Wang Yulu Huang Xiaoshuang Zhang Yilin Tang Qing Li Zhaolin Liu Yuanyuan Ma Jiabin Tong Li Huang Jian Fei Mei Yu Jian Wang Fang Huang Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models Redox Biology |
author_facet |
Zishan Wang Hongtian Dong Jinghui Wang Yulu Huang Xiaoshuang Zhang Yilin Tang Qing Li Zhaolin Liu Yuanyuan Ma Jiabin Tong Li Huang Jian Fei Mei Yu Jian Wang Fang Huang |
author_sort |
Zishan Wang |
title |
Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models |
title_short |
Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models |
title_full |
Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models |
title_fullStr |
Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models |
title_full_unstemmed |
Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease models |
title_sort |
pro-survival and anti-inflammatory roles of nf-κb c-rel in the parkinson's disease models |
publisher |
Elsevier |
series |
Redox Biology |
issn |
2213-2317 |
publishDate |
2020-02-01 |
description |
The pathological hallmarks of Parkinson's disease (PD) are the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc) and the presence of overactivated glial cells and neuroinflammation. Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) c-Rel subunit is closely related in the pathological progress of PD, however the roles and mechanisms of c-Rel in PD development remain unclear. Here, in neurotoxins-induced PD models, the dynamic changes of NF-κB c-Rel and its functions were evaluated. We found that c-Rel was rapidly activated in the nigrostriatal pathway, which mainly occurred in dopaminergic neurons and microglia. c-Rel could maintain neuronal survival by initiating the anti-apoptotic gene expression in MPP+-treated SH-SY5Y cells and it could inhibit microglial overactivation by suppressing the inflammatory gene expression in LPS-challenged BV2 cells. c-Rel inhibitor IT901 aggravated the damage of MPTP on dopaminergic neurons and promoted the activation of microglia in the nigrostriatal pathway of mice. Moreover, the expression of c-Rel in blood samples of PD patients decreased dramatically. Our results indicate that the NF-κB/c-Rel subunit plays an important role in neuroprotection and neuroinflammation inhibition during PD progression. Keywords: Parkinson's disease, NF-κB/c-Rel, Dopaminergic neurons, Microglia, Neuroprotection, Inflammation |
url |
http://www.sciencedirect.com/science/article/pii/S221323171931184X |
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doaj-5636ed92da3c4549990d28a5025cc45a2020-11-25T03:20:12ZengElsevierRedox Biology2213-23172020-02-0130Pro-survival and anti-inflammatory roles of NF-κB c-Rel in the Parkinson's disease modelsZishan Wang0Hongtian Dong1Jinghui Wang2Yulu Huang3Xiaoshuang Zhang4Yilin Tang5Qing Li6Zhaolin Liu7Yuanyuan Ma8Jiabin Tong9Li Huang10Jian Fei11Mei Yu12Jian Wang13Fang Huang14Department of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, ChinaSchool of Life Science and Technology, Tongji University, 1239 Siping Road, Shanghai, 200092, China; Shanghai Research Center for Model Organisms, Pudong, Shanghai, 201203, China; Shanghai Engineering Research Center for Model Organisms, Shanghai Model Organisms Center, INC., Shanghai, 201203, ChinaDepartment of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China; Corresponding author. State Key Laboratory of Medical Neurobiology, Shanghai Medical College, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China.Department of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China; Department of Neurology, Huashan Hospital, Fudan University, 12 Wulumuqi Zhong Road, Shanghai, 200040, China; Corresponding author. Department of Neurology, Huashan Hospital, Fudan University. 12 Wulumuqi Zhong Road, Shanghai, 200040, China.Department of Translational Neuroscience, Jing’ an District Centre Hospital of Shanghai, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China; Corresponding author. State Key Laboratory of Medical Neurobiology, Shanghai Medical College, Fudan University, 138 Yixueyuan Road, Shanghai, 200032, China.The pathological hallmarks of Parkinson's disease (PD) are the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc) and the presence of overactivated glial cells and neuroinflammation. Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) c-Rel subunit is closely related in the pathological progress of PD, however the roles and mechanisms of c-Rel in PD development remain unclear. Here, in neurotoxins-induced PD models, the dynamic changes of NF-κB c-Rel and its functions were evaluated. We found that c-Rel was rapidly activated in the nigrostriatal pathway, which mainly occurred in dopaminergic neurons and microglia. c-Rel could maintain neuronal survival by initiating the anti-apoptotic gene expression in MPP+-treated SH-SY5Y cells and it could inhibit microglial overactivation by suppressing the inflammatory gene expression in LPS-challenged BV2 cells. c-Rel inhibitor IT901 aggravated the damage of MPTP on dopaminergic neurons and promoted the activation of microglia in the nigrostriatal pathway of mice. Moreover, the expression of c-Rel in blood samples of PD patients decreased dramatically. Our results indicate that the NF-κB/c-Rel subunit plays an important role in neuroprotection and neuroinflammation inhibition during PD progression. Keywords: Parkinson's disease, NF-κB/c-Rel, Dopaminergic neurons, Microglia, Neuroprotection, Inflammationhttp://www.sciencedirect.com/science/article/pii/S221323171931184X |