The role of nitric oxide in the particulate matter (PM2.5)-induced NFκB activation in lung epithelial cells

• DOI: 10.1016/j.toxlet.2003.12.007
• Publication Date: 2004-02-11T05:12:47Z
• Authors: H Nam
• Keywords: Inflammation; Air Pollutants; 0303 health sciences; Cell Culture Techniques; NF-kappa B; 610; Epithelial Cells; Nitric Oxide; Reactive Nitrogen Species; 03 medical and health sciences; Nitric oxides; 616; 11. Sustainability; Humans; Nuclear factor κB; Nitric Oxide Synthase; Particle Size; Particulate matter; Inducible nitric oxide synthase; Reactive Oxygen Species; Lung

NFkappaB is one of key transcription factors that are involved in the inflammatory responses to the particulate matter (PM) in the lungs. In order to further understand the molecular mechanism, the effects of antioxidants and an inducible nitric oxide synthase (iNOS) inhibitor on PM-induced NFkappaB activation were examined in A549 lung epithelial cells. NFkappaB activation by 2.5 microm particulates (PM2.5) was evident from the degradation of an NFkappaB inhibitory protein, IkappaBalpha, and a luciferase reporter assay for NFkappaB activity. In these experiments, a pre-treatment of the cells with antioxidants N-acetyl-l-cysteine (NAC) and dimethylthiourea (DMTU) or an iNOS inhibitor l-N6-1-iminoethyl-lysine (L-NIL) clearly inhibited the NFkappaB activation by PM2.5. The inhibitory effect of L-NIL was also observed on the PM2.5-induced interleukin-8 (IL-8) gene expression both at the transcriptional and protein levels. These results suggest that PM2.5 induces NFkappaB activity via the pathways involving ROS and/or RNS generation. Considering the fact that NFkappaB also induces NO generation via iNOS expression, they might make a positive feedback loop that amplifies the downstream responses.