The induction of cyclo-oxygenase-2 in human pulmonary epithelial cell culture (A549) activated by IL-1β is inhibited by tyrosine kinase inhibitors

• Main Authors: P. Akarasereenont, C. Thiemermann
• Other Authors: Barts and The London Queen Mary's School of Medicine and Dentistry
• Format: Article
• Published: 2018
• Subjects: Biochemistry, Genetics and Molecular Biology
• Online Access: https://repository.li.mahidol.ac.th/handle/123456789/17546
• Institution: Mahidol University

Cyclo-oxygenase (COX) exists as two isoforms. In endothelial cells, the induction of COX (COX-2) elicited by endotoxin or inflammatory cytokines is mediated by tyrosine kinase. Here we have investigated whether the induction of COX-2 elicited by IL-1β in human pulmonary epithelial cells (A549) is mediated by tyrosine kinase. The activity of COX-2 was assessed by measuring the accumulation of PGE2by radioimmunoassay. The expression of COX-2 protein was detected by immunoblot using specific antibodies to COX-2. Untreated A549 cells contained no COX-2 protein and released low levels of PGE2(< 0.3 ng/ml for 24 h). A549 cells treated with IL-1β (0.01 to 10 ng/ml) contained COX-2 protein and released greater amounts of PGE2. The increased COX-2 protein and activity in response to IL-1β (10 ng/ml) was inhibited by the tyrosine kinase inhibitors tyrphostin (AG126; 0.015 to 15 μM) or erbstatin (0.004 to 4 μM). Thus, the induction of COX-2 by IL-1β in epithelial cells is mediated by tyrosine kinase.