IL-18 is induced and IL-18 receptor alpha plays a critical role in the pathogenesis of cigarette smoke-induced pulmonary emphysema and inflammation

J Immunol. 2007 Feb 1;178(3):1948-59. doi: 10.4049/jimmunol.178.3.1948.

Abstract

Th1 inflammation and remodeling characterized by local tissue destruction coexist in pulmonary emphysema and other diseases. To test the hypothesis that IL-18 plays an important role in these responses, we characterized the regulation of IL-18 in lungs from cigarette smoke (CS) and room air-exposed mice and characterized the effects of CS in wild-type mice and mice with null mutations of IL-18Ralpha (IL-18Ralpha(-/-)). CS was a potent stimulator and activator of IL-18 and caspases 1 and 11. In addition, although CS caused inflammation and emphysema in wild-type mice, both of these responses were significantly decreased in IL-18Ralpha(-/-) animals. CS also induced epithelial apoptosis, activated effector caspases and stimulated proteases and chemokines via IL-18Ralpha-dependent pathways. Importantly, the levels of IL-18 and its targets, cathepsins S and B, were increased in pulmonary macrophages from smokers and patients with chronic obstructive lung disease. Elevated levels of circulating IL-18 were also seen in patients with chronic obstructive lung disease. These studies demonstrate that IL-18 and the IL-18 pathway are activated in CS-exposed mice and man. They also demonstrate, in a murine modeling system, that IL-18R signaling plays a critical role in the pathogenesis of CS-induced inflammation and emphysema.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis
  • Caspases / metabolism
  • Chemokines / metabolism
  • Epithelial Cells
  • Humans
  • Inflammation / etiology*
  • Interleukin-18 / blood
  • Interleukin-18 / metabolism*
  • Mice
  • Mice, Knockout
  • Nicotiana
  • Peptide Hydrolases / metabolism
  • Pulmonary Emphysema / etiology*
  • Pulmonary Emphysema / pathology
  • Receptors, Interleukin-18 / genetics
  • Receptors, Interleukin-18 / metabolism*
  • Smoke / adverse effects*

Substances

  • Chemokines
  • Interleukin-18
  • Receptors, Interleukin-18
  • Smoke
  • Peptide Hydrolases
  • Caspases