Expression of Interleukin-18 in the Lung after Endotoxemia or Hemorrhage-Induced Acute Lung Injury

• Published in: American journal of respiratory cell and molecular biology Vol. 22; no. 6; pp. 708 - 713
• Main Authors: Arndt, Patrick G, Fantuzzi, Giamilla, Abraham, Edward
• Format: Journal Article
• Language: English
• Published: United States Am Thoracic Soc 01.06.2000; American Thoracic Society
• Subjects: Animals; Bronchoalveolar Lavage Fluid - immunology; Caspase 1 - genetics; Caspase 1 - immunology; Disease Models, Animal; Endotoxemia - immunology; Gene Expression Regulation, Enzymologic - immunology; Hemorrhage - immunology; Interferon-gamma - genetics; Interferon-gamma - immunology; Interleukin-12 - genetics; Interleukin-12 - immunology; Interleukin-18 - blood; Interleukin-18 - genetics; Interleukin-18 - immunology; Lung - enzymology; Lung - immunology; Male; Mice; Mice, Inbred BALB C; Respiratory Distress Syndrome, Adult - immunology; RNA, Messenger - analysis
• ISSN: 1044-1549; 1535-4989
• DOI: 10.1165/ajrcmb.22.6.3832

Hemorrhage and endotoxemia are important risk factors for the development of acute lung injury. Interleukin (IL)-18 is a recently described cytokine released in its mature, active form after pro-IL-18 is cleaved by the IL-1 converting enzyme (ICE). IL-18 has multiple immunomodulating properties, including induction of interferon-gamma (IFN-gamma), IL-1beta, tumor necrosis factor-alpha, and intercellular adhesion molecule-1. To examine the possible involvement of IL-18 in acute lung injury, we examined its expression, as well as that of IFN-gamma, IL-12, and ICE, using murine hemorrhage or endotoxemia models. The amounts of IL-18 messenger RNA (mRNA) increased in the lung after hemorrhage or endotoxemia. However, only endotoxemia was associated with elevations in lung and plasma concentrations of IL-18 protein. ICE expression was increased in the lungs after endotoxemia but not after hemorrhage. Although IFN-gamma expression increased in the lungs after hemorrhage or endotoxemia, elevations in lung IL-12 mRNA levels were found only after endotoxemia. These results indicate that hemorrhage and endotoxemia induce different patterns of immunomodulatory cytokine expression in the lungs. In particular, differences in the expression of ICE after hemorrhage or endotoxemia may affect generation of the active forms of downstream cytokines, including IL-18. IFN-gamma expression in the lungs after hemorrhage appears to occur through a pathway independent of IL-12 and IL-18. IL-18 may play a role in modulating the development of acute lung injury after endotoxemia but not after hemorrhage.