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American Journal of Respiratory Cell and Molecular Biology. Vol. 27, pp. 542-552, 2002
© 2002 American Thoracic Society
DOI: 10.1165/rcmb.4775

Hydrogen Peroxide Induces Upregulation of Fas in Human Airway Epithelial Cells via the Activation of PARP-p53 Pathway

Tadashi Fujita, Muneharu Maruyama, Jun Araya, Kazuhiko Sassa, Yukio Kawagishi, Ryuji Hayashi, Shoko Matsui, Tatsuhiko Kashii, Naohiro Yamashita, Eiji Sugiyama and Masashi Kobayashi

The First Department of Internal Medicine, Faculty of Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan

Address correspondence to: Muneharu Maruyama, M.D., The First Department of Internal Medicine, Faculty of Medicine, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan. E-mail: mmaruyam-tym{at}umin.ac.jp

Fas mediates apoptosis following binding with Fas ligand. Fas is expressed in human airway epithelial cells and has a critical role in the pathophysiology of various pulmonary disorders. Hydrogen peroxide (H2O2) is an important mediator of airway epithelial injury. In this context, we hypothesized that H2O2 would increase the expression of cell surface Fas in human airway epithelial cells. To test this hypothesis, the modulation of Fas expression with H2O2 was assessed in normal human bronchial epithelial cells and A549 cells. The majority of Fas was cytoplasmic in both cell types without any stimulation. Hydrogen peroxide significantly increased Fas in the plasma membrane fraction, while decreasing Fas in the cytoplasmic fraction. Incubation with an agonistic antibody for Fas induced apoptosis in H2O2-treated cells in proportion to the level of surface Fas expression on those cells. Inhibitors of poly(ADP-ribose) polymerase abrogated the H2O2-induced Fas translocation to the plasma membrane and p53 activation. Expression of dominant–negative p53 also inhibited the Fas translocation induced by H2O2 in A549 cells. These results indicate that H2O2 induces Fas upregulation by promoting cytoplasmic transport of Fas to the cell surface in human airway epithelial cells, and that the activation of the poly(ADP-ribose) polymerase-p53 pathway may be involved in this mechanism.

Abbreviations: antibodies, Abs • 3-aminobenzamide, 3-AB • bronchoalveolar lavage fluid, BALF • 4',6-diamidino-2'-phenylindol dihydrochloride, DAPI • Fas ligand, FasL • green fluorescent protein, GFP • hydrogen peroxide, H2O2 • immunoglobulin, Ig • idiopathic pulmonary fibrosis, IPF • monoclonal Abs, mAbs • mean fluorescence intensity, MFI • normal human bronchial epithelial, NHBE • superoxide anion, O2- • poly(ADP-ribose) polymerase, PARP • phosphate-buffered saline, PBS • phycoerythrin, PE • propidium iodide, PI • reactive oxygen species, ROS • tumor necrosis factor, TNF




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Proc. Am. Thorac. Soc. Am. J. Respir. Crit. Care Med.
Copyright © 2002 American Thoracic Society.
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