Abstract
Silica is a causative factor of acute cell injury in pulmonary fibrosis. Inducible cyclooxygenase-2 (COX-2) was suggested to play a role in the process of inflammation and fibrosis. We report that silica induces COX-2 expression in WI-38 fibroblasts. Further analysis showed that silica activated the transcription of COX-2 gene primarily via a nuclear factor (NF)-κB binding site in the promoter. NF-κB-inducing kinase (NIK) and TGF-κ activated kinase 1 (TAK1), the upstream signaling molecules of NF-κB, are involved in the silica-mediated COX-2 expression. The Electrophoretic Mobility Shift Assay (EMSA) showed that silica induced the direct binding of NF-κB on the putative binding site in COX-2 promoter. These results suggest that silica activates the human COX-2 gene transcription through the induction of NF-κB activity.
Original language | English |
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Pages (from-to) | 163-174 |
Number of pages | 12 |
Journal | Journal of Environmental Pathology, Toxicology and Oncology |
Volume | 24 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2005 |
Keywords
- COX-2
- NF-κB
- NIK
- Pulmonary fibrosis
- Pulmonary silicosis
- Silica
- TAK1