Published ahead of print on July 24, 2008, doi:10.1164/rccm.200712-1895OC Am. J. Respir. Crit. Care Med., Volume 178, Number 7, October 2008, 701-709 A more recent version of this article appeared on October 1, 2008
Submitted on December 26, 2007 Proteomic Analysis of Sequential Lung Lavage Proteins during the Acute Respiratory Distress SyndromeDong W Chang1,1 Medical Research Service of the VA Puget Sound Healthcare System, University of Washington, Seattle, WA, USA; Divisions of Pulmonary and Critical Care Medicine, University of Washington, Seattle, WA, USA, 2 Divisions of Pulmonary and Critical Care Medicine, University of Washington, Seattle, WA, USA, 3 Department of Endocrinology and Metabolism, University of Washington, Seattle, WA, USA, 4 Department of Microbiology, University of Washington, Seattle, WA, USA * To whom correspondence should be addressed. E-mail: trmartin{at}u.washington.edu.
Rationale: The purpose of this study was to examine the changes in protein expression in the bronchoalveolar lavage fluid (BALF) of patients during the course of the acute respiratory distress syndrome (ARDS). Methods: Using two dimensional difference gel electrophoresis (DIGE), the expression of proteins in the BALF from patients on days 1 (n=7), 3 (n=8), and 7 (n=5) of ARDS were compared to findings in normal volunteers (n=9). The patterns of protein expression were analyzed using principal component analysis (PCA). Biological processes that were enriched in the BALF proteins of patients with ARDS were identified using Gene Ontology analysis. Protein networks that model the protein interactions in the BALF were generated using Ingenuity Pathway Analysis. Results: An average of 991 protein spots were detected using DIGE. Of these, 80 protein spots, representing 37 unique proteins in all of the fluids, were identified using mass spectrometry. PCA confirmed important differences between the proteins in the ARDS and normal samples. GO analysis showed that these differences are due to the enrichment of proteins involved in inflammation, infection, and injury. The protein network analysis showed that the protein interactions in ARDS are complex and redundant, and revealed unexpected central components in the protein networks. Conclusion: Proteomics and protein network analyses reveal the complex nature of lung protein interactions in ARDS. The results provide new insights about protein networks in injured lungs, and identify novel mediators that are likely to be involved in the pathogenesis and progression of acute lung injury. Key words: Lung injury, Acute respiratory distress syndrome, Proteomics, Bronchoalveolar lavage, 2D gel electrophoresis,
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