Neutrophil proteinase 3-mediated induction of bioactive IL-18 secretion byhuman oral epithelial cells

Citation
S. Sugawara et al., Neutrophil proteinase 3-mediated induction of bioactive IL-18 secretion byhuman oral epithelial cells, J IMMUNOL, 167(11), 2001, pp. 6568-6575
Citations number
45
Categorie Soggetti
Immunology
Journal title
JOURNAL OF IMMUNOLOGY
ISSN journal
00221767 → ACNP
Volume
167
Issue
11
Year of publication
2001
Pages
6568 - 6575
Database
ISI
SICI code
0022-1767(200112)167:11<6568:NP3IOB>2.0.ZU;2-1
Abstract
IL-18, a potent IFN-gamma -inducing cytokine, is expressed by various nonim mune cells as well as macrophages, suggesting that it has important physiol ogical and immunological roles. The present study focused on the mechanism of active IL-18 induction from human oral epithelial cells. The epithelial cells and the cell lines constitutively express IL-18 mRNA and the 24-kDa p recursor form of IL-18. Bioactive IL-18 exhibiting IFN-gamma -inducing acti vity was detected in the supernatant of the cells on costimulation with neu trophil proteinase 3 (PR3) and LPS for 24 h after IFN-gamma -priming for 3 days. An active 18-kDa form of IL-18 was detected in lysate and supernatant of the cells only after the above treatment and the induction was inhibite d by cycloheximide and by serine proteinase inhibitors. After the treatment , lactate dehydrogenase activity was not detected in the cell culture super natant, and PR3 was detected only in the membrane and not in cytoplasm frac tions of the cells. Caspase-1 was not detected in the cells even after the treatment and the IL-18 induction was not inhibited by a caspase-1 inhibito r. These results suggest that the PR3-mediated induction of bioactive IL-18 secretion from oral epithelial cells in combination with LPS after IFN-gam ma -priming occurred via a caspase-1-independent pathway, and provide new i nsight into the possible involvement of a neutrophil proteinase in the indu ction of bioactive IL-18 in oral inflammation such as periodontitis.