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Published ahead of print on August 11, 2005, doi:10.1164/rccm.200502-286OC
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American Journal of Respiratory and Critical Care Medicine Vol 172. pp. 1399-1411, (2005)
© 2005 American Thoracic Society
doi: 10.1164/rccm.200502-286OC


Original Article

Gene Expression Changes during the Development of Acute Lung Injury Role of Transforming Growth Factor {beta}

Scott C. Wesselkamper, Lisa M. Case, Lisa N. Henning, Michael T. Borchers, Jay W. Tichelaar, John M. Mason, Nadine Dragin, Mario Medvedovic, Maureen A. Sartor, Craig R. Tomlinson and George D. Leikauf

Department of Environmental Health, Center for Environmental Genetics, and Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Cincinnati Medical Center, University of Cincinnati, Cincinnati, Ohio

Correspondence and requests for reprints should be addressed to George D. Leikauf, Ph.D., Department of Environmental Health, P.O. Box 670056, University of Cincinnati, Cincinnati, OH 45267-0056. E-mail: george.leikauf{at}uc.edu

Rationale: Acute lung injury can occur from multiple causes, resulting in high mortality. The pathophysiology of nickel-induced acute lung injury in mice is remarkably complex, and the molecular mechanisms are uncertain.

Objectives: To integrate molecular pathways and investigate the role of transforming growth factor {beta} (TGF-{beta}) in acute lung injury in mice.

Methods: cDNA microarray analyses were used to identify lung gene expression changes after nickel exposure. MAPPFinder analysis of the microarray data was used to determine significantly altered molecular pathways. TGF-{beta}1 protein in bronchoalveolar lavage fluid, as well as the effect of inhibition of TGF-{beta}, was assessed in nickel-exposed mice. The effect of TGF-{beta} on surfactant-associated protein B (Sftpb) promoter activity was measured in mouse lung epithelial cells.

Measurements and Main Results: Genes that decreased the most after nickel exposure play important roles in lung fluid absorption or surfactant and phospholipid synthesis, and genes that increased the most were involved in TGF-{beta} signaling. MAPPFinder analysis further established TGF-{beta} signaling to be significantly altered. TGF-{beta}–inducible genes involved in the regulation of extracellular matrix function and fibrinolysis were significantly increased after nickel exposure, and TGF-{beta}1 protein was also increased in the lavage fluid. Pharmacologic inhibition of TGF-{beta} attenuated nickel-induced protein in bronchoalveolar lavage. In addition, treatment with TGF-{beta}1 dose-dependently repressed Sftpb promoter activity in vitro, and a novel TGF-{beta}–responsive region in the Sftpb promoter was identified.

Conclusions: These data suggest that TGF-{beta} acts as a central mediator of acute lung injury through the alteration of several different molecular pathways.

Key Words: microarray • surfactant • fibrinolysis • extracellular matrix




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