Cargando…

Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease

Aberrant antioxidant activity and excessive deposition of extracellular matrix (ECM) are hallmarks of interstitial lung diseases (ILD). It is known that oxidative stress alters the ECM, but extracellular antioxidant defence mechanisms in ILD are incompletely understood. Here, we extracted abundance...

Descripción completa

Detalles Bibliográficos
Autores principales: Schamberger, Andrea C., Schiller, Herbert B., Fernandez, Isis E., Sterclova, Martina, Heinzelmann, Katharina, Hennen, Elisabeth, Hatz, Rudolf, Behr, Jürgen, Vašáková, Martina, Mann, Matthias, Eickelberg, Oliver, Staab-Weijnitz, Claudia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951690/
https://www.ncbi.nlm.nih.gov/pubmed/27435875
http://dx.doi.org/10.1038/srep29952
_version_ 1782443747367190528
author Schamberger, Andrea C.
Schiller, Herbert B.
Fernandez, Isis E.
Sterclova, Martina
Heinzelmann, Katharina
Hennen, Elisabeth
Hatz, Rudolf
Behr, Jürgen
Vašáková, Martina
Mann, Matthias
Eickelberg, Oliver
Staab-Weijnitz, Claudia A.
author_facet Schamberger, Andrea C.
Schiller, Herbert B.
Fernandez, Isis E.
Sterclova, Martina
Heinzelmann, Katharina
Hennen, Elisabeth
Hatz, Rudolf
Behr, Jürgen
Vašáková, Martina
Mann, Matthias
Eickelberg, Oliver
Staab-Weijnitz, Claudia A.
author_sort Schamberger, Andrea C.
collection PubMed
description Aberrant antioxidant activity and excessive deposition of extracellular matrix (ECM) are hallmarks of interstitial lung diseases (ILD). It is known that oxidative stress alters the ECM, but extracellular antioxidant defence mechanisms in ILD are incompletely understood. Here, we extracted abundance and detergent solubility of extracellular antioxidant enzymes from a proteomic dataset of bleomycin-induced lung fibrosis in mice and assessed regulation and distribution of glutathione peroxidase 3 (GPX3) in murine and human lung fibrosis. Superoxide dismutase 3 (Sod3), Gpx3, and Gpx activity were increased in mouse BALF during bleomycin-induced lung fibrosis. In lung tissue homogenates, Gpx3, but not Sod3, was upregulated and detergent solubility profiling indicated that Gpx3 associated with ECM proteins. Immunofluorescence analysis showed that Gpx3 was expressed by bronchial epithelial cells and interstitial fibroblasts and localized to the basement membrane and interstitial ECM in lung tissue. As to human ILD samples, BALF of some patients contained high levels of GPX3, and GPX3 was upregulated in lung homogenates from IPF patients. GPX3 expression in primary human bronchial epithelial cells and lung fibroblasts was downregulated by TNF-α, but more variably regulated by TGF-β1 and menadione. In conclusion, the antioxidant enzyme GPX3 localizes to lung ECM and is variably upregulated in ILD.
format Online
Article
Text
id pubmed-4951690
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49516902016-07-26 Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease Schamberger, Andrea C. Schiller, Herbert B. Fernandez, Isis E. Sterclova, Martina Heinzelmann, Katharina Hennen, Elisabeth Hatz, Rudolf Behr, Jürgen Vašáková, Martina Mann, Matthias Eickelberg, Oliver Staab-Weijnitz, Claudia A. Sci Rep Article Aberrant antioxidant activity and excessive deposition of extracellular matrix (ECM) are hallmarks of interstitial lung diseases (ILD). It is known that oxidative stress alters the ECM, but extracellular antioxidant defence mechanisms in ILD are incompletely understood. Here, we extracted abundance and detergent solubility of extracellular antioxidant enzymes from a proteomic dataset of bleomycin-induced lung fibrosis in mice and assessed regulation and distribution of glutathione peroxidase 3 (GPX3) in murine and human lung fibrosis. Superoxide dismutase 3 (Sod3), Gpx3, and Gpx activity were increased in mouse BALF during bleomycin-induced lung fibrosis. In lung tissue homogenates, Gpx3, but not Sod3, was upregulated and detergent solubility profiling indicated that Gpx3 associated with ECM proteins. Immunofluorescence analysis showed that Gpx3 was expressed by bronchial epithelial cells and interstitial fibroblasts and localized to the basement membrane and interstitial ECM in lung tissue. As to human ILD samples, BALF of some patients contained high levels of GPX3, and GPX3 was upregulated in lung homogenates from IPF patients. GPX3 expression in primary human bronchial epithelial cells and lung fibroblasts was downregulated by TNF-α, but more variably regulated by TGF-β1 and menadione. In conclusion, the antioxidant enzyme GPX3 localizes to lung ECM and is variably upregulated in ILD. Nature Publishing Group 2016-07-20 /pmc/articles/PMC4951690/ /pubmed/27435875 http://dx.doi.org/10.1038/srep29952 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schamberger, Andrea C.
Schiller, Herbert B.
Fernandez, Isis E.
Sterclova, Martina
Heinzelmann, Katharina
Hennen, Elisabeth
Hatz, Rudolf
Behr, Jürgen
Vašáková, Martina
Mann, Matthias
Eickelberg, Oliver
Staab-Weijnitz, Claudia A.
Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title_full Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title_fullStr Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title_full_unstemmed Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title_short Glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
title_sort glutathione peroxidase 3 localizes to the epithelial lining fluid and the extracellular matrix in interstitial lung disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951690/
https://www.ncbi.nlm.nih.gov/pubmed/27435875
http://dx.doi.org/10.1038/srep29952
work_keys_str_mv AT schambergerandreac glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT schillerherbertb glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT fernandezisise glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT sterclovamartina glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT heinzelmannkatharina glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT hennenelisabeth glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT hatzrudolf glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT behrjurgen glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT vasakovamartina glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT mannmatthias glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT eickelbergoliver glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease
AT staabweijnitzclaudiaa glutathioneperoxidase3localizestotheepithelialliningfluidandtheextracellularmatrixininterstitiallungdisease