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1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation
1-Nitropyrene (1-NP), one of the most abundant nitropolycyclic aromatic hydrocarbons (nitro-PAHs), is generated from the incomplete combustion of carbonaceous organic compounds. 1-NP is a specific marker of diesel exhaust and is an environmental pollutant and a probable carcinogen. Macrophages parti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294986/ https://www.ncbi.nlm.nih.gov/pubmed/34336119 http://dx.doi.org/10.1155/2021/9314342 |
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author | Su, Chun-Hung Ho, Yung-Chuan Lee, Min-Wei Tseng, Ching-Chi Lee, Shiuan-Shinn Hsieh, Ming Kun Chen, Hsin-Hung Lee, Chien-Ying Wu, Sheng-Wen Kuan, Yu-Hsiang |
author_facet | Su, Chun-Hung Ho, Yung-Chuan Lee, Min-Wei Tseng, Ching-Chi Lee, Shiuan-Shinn Hsieh, Ming Kun Chen, Hsin-Hung Lee, Chien-Ying Wu, Sheng-Wen Kuan, Yu-Hsiang |
author_sort | Su, Chun-Hung |
collection | PubMed |
description | 1-Nitropyrene (1-NP), one of the most abundant nitropolycyclic aromatic hydrocarbons (nitro-PAHs), is generated from the incomplete combustion of carbonaceous organic compounds. 1-NP is a specific marker of diesel exhaust and is an environmental pollutant and a probable carcinogen. Macrophages participate in immune defense against the invasive pathogens in heart, lung, and kidney infection diseases. However, no evidence has indicated that 1-NP induces apoptosis in macrophages. In the present study, 1-NP was found to induce concentration-dependent changes in various cellular functions of RAW264.7 macrophages including cell viability reduction; apoptosis generation; mitochondrial dysfunction; apoptosis-inducing factor (AIF) nuclear translocation; intracellular ROS generation; activation of the AMPK/Nrf-2/HO-1 pathway; changes in the expression of BCL-2 family proteins; and depletion of antioxidative enzymes (AOE), such as glutathione peroxidase (GPx), catalase (CAT), and superoxide dismutase (SOD) These results indicate that 1-NP induced apoptosis in macrophages through AIF nuclear translocation and ROS generation due to mitochondrial dysfunction and to the depletion of AOE from the activation of the AMPK/Nrf-2/HO-1 pathway. |
format | Online Article Text |
id | pubmed-8294986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-82949862021-07-31 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation Su, Chun-Hung Ho, Yung-Chuan Lee, Min-Wei Tseng, Ching-Chi Lee, Shiuan-Shinn Hsieh, Ming Kun Chen, Hsin-Hung Lee, Chien-Ying Wu, Sheng-Wen Kuan, Yu-Hsiang Oxid Med Cell Longev Research Article 1-Nitropyrene (1-NP), one of the most abundant nitropolycyclic aromatic hydrocarbons (nitro-PAHs), is generated from the incomplete combustion of carbonaceous organic compounds. 1-NP is a specific marker of diesel exhaust and is an environmental pollutant and a probable carcinogen. Macrophages participate in immune defense against the invasive pathogens in heart, lung, and kidney infection diseases. However, no evidence has indicated that 1-NP induces apoptosis in macrophages. In the present study, 1-NP was found to induce concentration-dependent changes in various cellular functions of RAW264.7 macrophages including cell viability reduction; apoptosis generation; mitochondrial dysfunction; apoptosis-inducing factor (AIF) nuclear translocation; intracellular ROS generation; activation of the AMPK/Nrf-2/HO-1 pathway; changes in the expression of BCL-2 family proteins; and depletion of antioxidative enzymes (AOE), such as glutathione peroxidase (GPx), catalase (CAT), and superoxide dismutase (SOD) These results indicate that 1-NP induced apoptosis in macrophages through AIF nuclear translocation and ROS generation due to mitochondrial dysfunction and to the depletion of AOE from the activation of the AMPK/Nrf-2/HO-1 pathway. Hindawi 2021-07-13 /pmc/articles/PMC8294986/ /pubmed/34336119 http://dx.doi.org/10.1155/2021/9314342 Text en Copyright © 2021 Chun-Hung Su et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Su, Chun-Hung Ho, Yung-Chuan Lee, Min-Wei Tseng, Ching-Chi Lee, Shiuan-Shinn Hsieh, Ming Kun Chen, Hsin-Hung Lee, Chien-Ying Wu, Sheng-Wen Kuan, Yu-Hsiang 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title | 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title_full | 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title_fullStr | 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title_full_unstemmed | 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title_short | 1-Nitropyrene Induced Reactive Oxygen Species–Mediated Apoptosis in Macrophages through AIF Nuclear Translocation and AMPK/Nrf-2/HO-1 Pathway Activation |
title_sort | 1-nitropyrene induced reactive oxygen species–mediated apoptosis in macrophages through aif nuclear translocation and ampk/nrf-2/ho-1 pathway activation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294986/ https://www.ncbi.nlm.nih.gov/pubmed/34336119 http://dx.doi.org/10.1155/2021/9314342 |
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