The Journal of Experimental Medicine
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Published online 18 September 2000.
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© The Rockefeller University Press, 0022-1007/2000/9/857/ $5.00
The Journal of Experimental Medicine, Volume 192, Number 6, September 18, 2000 857-870

Original Article

Nitric Oxide–Dependent Activation of P53 Suppresses Bleomycin-Induced Apoptosis in the Lung

Darren W. Davisa,b, Douglas A. Weidnerc, Andrij Holiana,d, and David J. McConkeya,b

a Program in Toxicology, University of Texas-Houston Graduate School of Biomedical Sciences, Houston, Texas 77030
b Department of Cancer Biology, University of Texas-MD Anderson Cancer Center, Houston, Texas 77030
c Department of Molecular Hematology and Therapy, University of Texas-MD Anderson Cancer Center, Houston, Texas 77030
d Department of Pulmonary and Critical Care Medicine, University of Texas Medical School, Houston, Texas 77030
Department of Cancer Biology-173, U.T. M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030.713-792-8747713-792-8591

Chronic inflammation leading to pulmonary fibrosis develops in response to environmental pollutants, radiotherapy, or certain cancer chemotherapeutic agents. We speculated that lung injury might be mediated by p53, a proapoptotic transcription factor widely implicated in the response of cells to DNA damage. Intratracheal administration of bleomycin led to caspase-mediated DNA fragmentation characteristic of apoptosis. The effects of bleomycin were associated with translocation of p53 from the cytosol to the nucleus only in alveolar macrophages that had been exposed to the drug in vivo, suggesting that the lung microenvironment regulated p53 activation. Experiments with a thiol antioxidant (N-acetylcysteine) in vivo and nitric oxide (NO) donors in vitro confirmed that reactive oxygen species were required for p53 activation. A specific role for NO was demonstrated in experiments with inducible nitric oxide synthase (iNOS)–/– macrophages, which failed to demonstrate nuclear p53 localization after in vivo bleomycin exposure. Strikingly, rates of bleomycin-induced apoptosis were at least twofold higher in p53–/– C57BL/6 mice compared with heterozygous or wild-type littermates. Similarly, levels of apoptosis were also twofold higher in the lungs of iNOS–/– mice than were observed in wild-type controls. Consistent with a role for apoptosis in chronic lung injury, levels of bleomycin-induced inflammation were substantially higher in iNOS–/– and p53–/– mice compared with wild-type controls. Together, our results demonstrate that iNOS and p53 mediate a novel apoptosis-suppressing pathway in the lung.

Key Words: NOS-2 • TUNEL • macrophage • oxygen radical • inflammation

Abbreviations used in this paper: iNOS, inducible nitric oxide synthase; LSC, laser scanning cytometer; NAC, N-acetylcysteine; PI, propidium iodide; SNAP, s-nitrosoaminopereillamine; TUNEL, TdT-uridine nick end labeling.

© 2000 The Rockefeller University Press


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