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. 1998 Oct;106(Suppl 5):1175–1178. doi: 10.1289/ehp.98106s51175

Increased nitric oxide synthase in the lung after ozone inhalation is associated with activation of NF-kappa B.

D L Laskin 1, V Sunil 1, Y Guo 1, D E Heck 1, J D Laskin 1
PMCID: PMC1533360  PMID: 9788894

Abstract

Acute inhalation of ozone is associated with a inflammatory response characterized by the accumulation of macrophages at sites of tissue injury. These cells, along with resident alveolar epithelial cells, become activated and release cytotoxic and proinflammatory mediators, such as nitric oxide (.NO), that we speculate contribute to toxicity. In these studies we analyzed mechanisms regulating increased .NO synthase activity in lung macrophages and type II cells after ozone inhalation. Brief exposure of rats to ozone (2 ppm for 3 hr) resulted in an increase in .NO production by alveolar macrophages as well as type II cells in response to the inflammatory mediators lipopolysaccharide and interferon gamma. These effects were apparently due to increased expression of inducible .NO synthase (iNOS) protein and mRNA, which were evident in vitro and in situ in histologic sections. .NO production and iNOS protein expression by both macrophages and epithelial cells were blocked by pyrrolidine dithiocarbamate (PDTC), an agent that inhibits activity of nuclear transcription factor kappa B (NF-kappa B). Cells from ozone-treated animals were less sensitive to the effects of PDTC than cells from control animals. Using electrophoretic mobility shift assays, we measured NF-kappa B binding activity in nuclear extracts of cells from control and ozone-exposed animals. Treatment of rats with ozone resulted in a time-dependent increase in NF-kappa B binding activity in both cell types, reaching a maximum in cells isolated 12 to 24 hr after ozone inhalation. Taken together, these data suggest that changes in the activity of NF-kappa B signaling are important in the response of lung macrophages and type II epithelial cells to cytokines after ozone inhalation.

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Selected References

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  1. Beckman J. S., Crow J. P. Pathological implications of nitric oxide, superoxide and peroxynitrite formation. Biochem Soc Trans. 1993 May;21(2):330–334. doi: 10.1042/bst0210330. [DOI] [PubMed] [Google Scholar]
  2. Dobbs L. G., Gonzalez R., Williams M. C. An improved method for isolating type II cells in high yield and purity. Am Rev Respir Dis. 1986 Jul;134(1):141–145. doi: 10.1164/arrd.1986.134.1.141. [DOI] [PubMed] [Google Scholar]
  3. Green L. C., Wagner D. A., Glogowski J., Skipper P. L., Wishnok J. S., Tannenbaum S. R. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids. Anal Biochem. 1982 Oct;126(1):131–138. doi: 10.1016/0003-2697(82)90118-x. [DOI] [PubMed] [Google Scholar]
  4. Grimminger F., von Kürten I., Walmrath D., Seeger W. Type II alveolar epithelial eicosanoid metabolism: predominance of cyclooxygenase pathways and transcellular lipoxygenase metabolism in co-culture with neutrophils. Am J Respir Cell Mol Biol. 1992 Jan;6(1):9–16. doi: 10.1165/ajrcmb/6.1.9. [DOI] [PubMed] [Google Scholar]
  5. Janssen Y. M., Barchowsky A., Treadwell M., Driscoll K. E., Mossman B. T. Asbestos induces nuclear factor kappa B (NF-kappa B) DNA-binding activity and NF-kappa B-dependent gene expression in tracheal epithelial cells. Proc Natl Acad Sci U S A. 1995 Aug 29;92(18):8458–8462. doi: 10.1073/pnas.92.18.8458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Laskin D. L., Pendino K. J. Macrophages and inflammatory mediators in tissue injury. Annu Rev Pharmacol Toxicol. 1995;35:655–677. doi: 10.1146/annurev.pa.35.040195.003255. [DOI] [PubMed] [Google Scholar]
  7. Laskin DL, Laskin JD. Macrophages, Inflammatory Mediators, and Lung Injury. Methods. 1996 Aug;10(1):61–70. doi: 10.1006/meth.1996.0079. [DOI] [PubMed] [Google Scholar]
  8. Lavnikova N., Prokhorova S., Helyar L., Laskin D. L. Isolation and partial characterization of subpopulations of alveolar macrophages, granulocytes, and highly enriched interstitial macrophages from rat lung. Am J Respir Cell Mol Biol. 1993 Apr;8(4):384–392. doi: 10.1165/ajrcmb/8.4.384. [DOI] [PubMed] [Google Scholar]
  9. Lavnikova N., Prokhorova S., Lakhotia A. V., Gordon R., Laskin D. L. Distinct inflammatory responses of adherent vascular lung neutrophils to pulmonary irritants. J Inflamm. 1998;48(2):56–66. [PubMed] [Google Scholar]
  10. Nathan C. Nitric oxide as a secretory product of mammalian cells. FASEB J. 1992 Sep;6(12):3051–3064. [PubMed] [Google Scholar]
  11. Paine R., 3rd, Rolfe M. W., Standiford T. J., Burdick M. D., Rollins B. J., Strieter R. M. MCP-1 expression by rat type II alveolar epithelial cells in primary culture. J Immunol. 1993 May 15;150(10):4561–4570. [PubMed] [Google Scholar]
  12. Pendino K. J., Gardner C. R., Shuler R. L., Laskin J. D., Durham S. K., Barton D. S., Ohnishi S. T., Ohnishi T., Laskin D. L. Inhibition of ozone-induced nitric oxide synthase expression in the lung by endotoxin. Am J Respir Cell Mol Biol. 1996 Jun;14(6):516–525. doi: 10.1165/ajrcmb.14.6.8652180. [DOI] [PubMed] [Google Scholar]
  13. Pendino K. J., Laskin J. D., Shuler R. L., Punjabi C. J., Laskin D. L. Enhanced production of nitric oxide by rat alveolar macrophages after inhalation of a pulmonary irritant is associated with increased expression of nitric oxide synthase. J Immunol. 1993 Dec 15;151(12):7196–7205. [PubMed] [Google Scholar]
  14. Pendino K. J., Meidhof T. M., Heck D. E., Laskin J. D., Laskin D. L. Inhibition of macrophages with gadolinium chloride abrogates ozone-induced pulmonary injury and inflammatory mediator production. Am J Respir Cell Mol Biol. 1995 Aug;13(2):125–132. doi: 10.1165/ajrcmb.13.2.7542894. [DOI] [PubMed] [Google Scholar]
  15. Pendino K. J., Shuler R. L., Laskin J. D., Laskin D. L. Enhanced production of interleukin-1, tumor necrosis factor-alpha, and fibronectin by rat lung phagocytes following inhalation of a pulmonary irritant. Am J Respir Cell Mol Biol. 1994 Sep;11(3):279–286. doi: 10.1165/ajrcmb.11.3.8086166. [DOI] [PubMed] [Google Scholar]
  16. Punjabi C. J., Laskin J. D., Pendino K. J., Goller N. L., Durham S. K., Laskin D. L. Production of nitric oxide by rat type II pneumocytes: increased expression of inducible nitric oxide synthase following inhalation of a pulmonary irritant. Am J Respir Cell Mol Biol. 1994 Aug;11(2):165–172. doi: 10.1165/ajrcmb.11.2.7519435. [DOI] [PubMed] [Google Scholar]
  17. Radi R., Beckman J. S., Bush K. M., Freeman B. A. Peroxynitrite oxidation of sulfhydryls. The cytotoxic potential of superoxide and nitric oxide. J Biol Chem. 1991 Mar 5;266(7):4244–4250. [PubMed] [Google Scholar]
  18. Schreck R., Meier B., Männel D. N., Dröge W., Baeuerle P. A. Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells. J Exp Med. 1992 May 1;175(5):1181–1194. doi: 10.1084/jem.175.5.1181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Standiford T. J., Kunkel S. L., Basha M. A., Chensue S. W., Lynch J. P., 3rd, Toews G. B., Westwick J., Strieter R. M. Interleukin-8 gene expression by a pulmonary epithelial cell line. A model for cytokine networks in the lung. J Clin Invest. 1990 Dec;86(6):1945–1953. doi: 10.1172/JCI114928. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Wulczyn F. G., Krappmann D., Scheidereit C. The NF-kappa B/Rel and I kappa B gene families: mediators of immune response and inflammation. J Mol Med (Berl) 1996 Dec;74(12):749–769. doi: 10.1007/s001090050078. [DOI] [PubMed] [Google Scholar]
  21. Xie Q. W., Kashiwabara Y., Nathan C. Role of transcription factor NF-kappa B/Rel in induction of nitric oxide synthase. J Biol Chem. 1994 Feb 18;269(7):4705–4708. [PubMed] [Google Scholar]

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