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Alterations in the human lung proteome with lipopolysaccharide
BACKGROUND: Recombinant human activated protein C (rhAPC) is associated with improved survival in high-risk patients with severe sepsis; however, the effects of both lipopolysaccharide (LPS) and rhAPC on the bronchoalveolar lavage fluid (BALF) proteome are unknown. METHODS: Using differential in gel...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694759/ https://www.ncbi.nlm.nih.gov/pubmed/19432985 http://dx.doi.org/10.1186/1471-2466-9-20 |
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author | Bowler, Russell P Reisdorph, Nichole Reisdorph, Richard Abraham, Edward |
author_facet | Bowler, Russell P Reisdorph, Nichole Reisdorph, Richard Abraham, Edward |
author_sort | Bowler, Russell P |
collection | PubMed |
description | BACKGROUND: Recombinant human activated protein C (rhAPC) is associated with improved survival in high-risk patients with severe sepsis; however, the effects of both lipopolysaccharide (LPS) and rhAPC on the bronchoalveolar lavage fluid (BALF) proteome are unknown. METHODS: Using differential in gel electrophoresis (DIGE) we identified changes in the BALF proteome from 10 healthy volunteers given intrapulmonary LPS in one lobe and saline in another lobe. Subjects were randomized to pretreatment with saline or rhAPC. RESULTS: An average of 255 protein spots were detected in each proteome. We found 31 spots corresponding to 8 proteins that displayed abundance increased or decreased at least 2-fold after LPS. Proteins that decreased after LPS included surfactant protein A, immunoglobulin J chain, fibrinogen-γ, α(1)-antitrypsin, immunoglobulin, and α(2)-HS-glycoprotein. Haptoglobin increased after LPS-treatment. Treatment with rhAPC was associated with a larger relative decrease in immunoglobulin J chain, fibrinogen-γ, α(1)-antitrypsin, and α(2)-HS-glycoprotein. CONCLUSION: Intrapulmonary LPS was associated with specific protein changes suggesting that the lung response to LPS is more than just a loss of integrity in the alveolar epithelial barrier; however, pretreatment with rhAPC resulted in minor changes in relative BALF protein abundance consistent with its lack of affect in ALI and milder forms of sepsis. |
format | Text |
id | pubmed-2694759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26947592009-06-11 Alterations in the human lung proteome with lipopolysaccharide Bowler, Russell P Reisdorph, Nichole Reisdorph, Richard Abraham, Edward BMC Pulm Med Research Article BACKGROUND: Recombinant human activated protein C (rhAPC) is associated with improved survival in high-risk patients with severe sepsis; however, the effects of both lipopolysaccharide (LPS) and rhAPC on the bronchoalveolar lavage fluid (BALF) proteome are unknown. METHODS: Using differential in gel electrophoresis (DIGE) we identified changes in the BALF proteome from 10 healthy volunteers given intrapulmonary LPS in one lobe and saline in another lobe. Subjects were randomized to pretreatment with saline or rhAPC. RESULTS: An average of 255 protein spots were detected in each proteome. We found 31 spots corresponding to 8 proteins that displayed abundance increased or decreased at least 2-fold after LPS. Proteins that decreased after LPS included surfactant protein A, immunoglobulin J chain, fibrinogen-γ, α(1)-antitrypsin, immunoglobulin, and α(2)-HS-glycoprotein. Haptoglobin increased after LPS-treatment. Treatment with rhAPC was associated with a larger relative decrease in immunoglobulin J chain, fibrinogen-γ, α(1)-antitrypsin, and α(2)-HS-glycoprotein. CONCLUSION: Intrapulmonary LPS was associated with specific protein changes suggesting that the lung response to LPS is more than just a loss of integrity in the alveolar epithelial barrier; however, pretreatment with rhAPC resulted in minor changes in relative BALF protein abundance consistent with its lack of affect in ALI and milder forms of sepsis. BioMed Central 2009-05-11 /pmc/articles/PMC2694759/ /pubmed/19432985 http://dx.doi.org/10.1186/1471-2466-9-20 Text en Copyright © 2009 Bowler et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bowler, Russell P Reisdorph, Nichole Reisdorph, Richard Abraham, Edward Alterations in the human lung proteome with lipopolysaccharide |
title | Alterations in the human lung proteome with lipopolysaccharide |
title_full | Alterations in the human lung proteome with lipopolysaccharide |
title_fullStr | Alterations in the human lung proteome with lipopolysaccharide |
title_full_unstemmed | Alterations in the human lung proteome with lipopolysaccharide |
title_short | Alterations in the human lung proteome with lipopolysaccharide |
title_sort | alterations in the human lung proteome with lipopolysaccharide |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694759/ https://www.ncbi.nlm.nih.gov/pubmed/19432985 http://dx.doi.org/10.1186/1471-2466-9-20 |
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