Benzo[]pyrene induces NLRP1 expression and promotes prolonged inflammasome signaling.

Front Immunol

Laboratory of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan.

Published: May 2023

AI Article Synopsis

  • Benzo[]pyrene (BaP) is a harmful air pollutant that causes inflammation in lung cells, specifically in the alveolar epithelium, by increasing NLRP1 expression while slightly reducing NLRP3 levels.
  • BaP's effects on NLRP1 expression were linked to the aryl hydrocarbon receptor (AhR) and reactive oxygen species (ROS), suggesting that these pathways are involved in the inflammatory response.
  • The study concluded that BaP could likely activate the NLRP1 inflammasome, contributing to ongoing lung inflammation from air pollution.

Article Abstract

Benzo[]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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192748PMC
http://dx.doi.org/10.3389/fimmu.2023.1154857DOI Listing

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