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Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling
Benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon in the air, triggers pulmonary inflammation. This study focused on BaP-induced inflammation in the alveolar epithelium. A549 cells were stimulated with BaP for four days. BaP treatment markedly increased NLRP1 expression but slightly decreased...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192748/ https://www.ncbi.nlm.nih.gov/pubmed/37215119 http://dx.doi.org/10.3389/fimmu.2023.1154857 |
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author | Kohno, Risa Nagata, Yuka Ishihara, Tomohiro Amma, Chisato Inomata, Yayoi Seto, Takafumi Suzuki, Ryo |
author_facet | Kohno, Risa Nagata, Yuka Ishihara, Tomohiro Amma, Chisato Inomata, Yayoi Seto, Takafumi Suzuki, Ryo |
author_sort | Kohno, Risa |
collection | PubMed |
description | Benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon in the air, triggers pulmonary inflammation. This study focused on BaP-induced inflammation in the alveolar epithelium. A549 cells were stimulated with BaP for four days. BaP treatment markedly increased NLRP1 expression but slightly decreased NLRP3. Furthermore, aryl hydrocarbon receptor (AhR) knockdown displayed no increase in BaP-induced NLRP1 expression. Similar results were also observed by blocking reactive oxygen species (ROS), which is mediated through AhR, suggesting that the AhR-ROS axis operates in BaP-induced NLRP1 expression. p53 involvement in ROS-mediated NLRP1 induction has also been implied. When we confirmed inflammasome activation in cells treated with BaP for four days, while BaP transiently activated NLRP3, it predominantly activated the NLRP1 inflammasome. These findings have led to the conclusion that BaP could be a potential ligand for the NLRP1 inflammasome persistently observed in the lung epithelium. Our study may provide additional evidence for the sustained pulmonary inflammation caused by environmental air pollution. |
format | Online Article Text |
id | pubmed-10192748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101927482023-05-19 Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling Kohno, Risa Nagata, Yuka Ishihara, Tomohiro Amma, Chisato Inomata, Yayoi Seto, Takafumi Suzuki, Ryo Front Immunol Immunology Benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon in the air, triggers pulmonary inflammation. This study focused on BaP-induced inflammation in the alveolar epithelium. A549 cells were stimulated with BaP for four days. BaP treatment markedly increased NLRP1 expression but slightly decreased NLRP3. Furthermore, aryl hydrocarbon receptor (AhR) knockdown displayed no increase in BaP-induced NLRP1 expression. Similar results were also observed by blocking reactive oxygen species (ROS), which is mediated through AhR, suggesting that the AhR-ROS axis operates in BaP-induced NLRP1 expression. p53 involvement in ROS-mediated NLRP1 induction has also been implied. When we confirmed inflammasome activation in cells treated with BaP for four days, while BaP transiently activated NLRP3, it predominantly activated the NLRP1 inflammasome. These findings have led to the conclusion that BaP could be a potential ligand for the NLRP1 inflammasome persistently observed in the lung epithelium. Our study may provide additional evidence for the sustained pulmonary inflammation caused by environmental air pollution. Frontiers Media S.A. 2023-05-04 /pmc/articles/PMC10192748/ /pubmed/37215119 http://dx.doi.org/10.3389/fimmu.2023.1154857 Text en Copyright © 2023 Kohno, Nagata, Ishihara, Amma, Inomata, Seto and Suzuki https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Kohno, Risa Nagata, Yuka Ishihara, Tomohiro Amma, Chisato Inomata, Yayoi Seto, Takafumi Suzuki, Ryo Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title | Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title_full | Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title_fullStr | Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title_full_unstemmed | Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title_short | Benzo[a]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling |
title_sort | benzo[a]pyrene induces nlrp1 expression and promotes prolonged inflammasome signaling |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192748/ https://www.ncbi.nlm.nih.gov/pubmed/37215119 http://dx.doi.org/10.3389/fimmu.2023.1154857 |
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