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(American Journal of Pathology. 2004;164:1949-1958.)
© 2004 American Society for Investigative Pathology

Differential Response of Human Lung Epithelial Cells to Fas-Induced Apoptosis

Morio Nakamura^*, Gustavo Matute-Bello^*, W. Conrad Liles, Shinichi Hayashi^*, Osamu Kajikawa^*, Shu-Min Lin^*, Charles W. Frevert^* and Thomas R. Martin^*

From the Medical Research Service of the Veterans Affairs/Puget Sound Health Care System,^*and the Divisions of Pulmonary and Critical Care Medicineand Allergy and Infectious Diseases,Department of Medicine, University of Washington School of Medicine, Seattle, Washington.

The Fas (CD95)/Fas ligand (CD178) system plays an important role in epithelial damage during the acute respiratory distress syndrome. The goal of this study was to determine whether proximal and distal human lung epithelial cells differ in their sensitivity to Fas ligand (rh-sFasL), and whether the response of lung epithelium to Fas ligation is modulated by proinflammatory cytokines. Although the expression of both Fas message and protein was similar in proximal and distal lung epithelial cells, only distal cells became apoptotic when exposed to serial dilutions of rh-sFasL. Stimulation with tumor necrosis factor-, interleukin-1ß, or interferon- significantly increased the sensitivity of proximal cells to rh-sFasL, and exposure to either tumor necrosis factor- or interferon- enhanced the sensitivity of distal cells to Fas ligation. These findings suggest that in normal human lungs, the responses of the epithelium to Fas ligation become more pronounced from proximal to distal locations. Furthermore, proinflammatory cytokines sensitize lung epithelium to Fas-induced death. These findings are relevant for understanding the role of the Fas/FasL system in acute lung injury, in which epithelial damage occurs primarily in distal airway and alveolar epithelium, whereas sFasL is present throughout the airspaces.

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