Cargando…
Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury
Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease characterized by epithelial cell activation, expansion of the fibroblast population and excessive extracellular matrix accumulation. The mechanisms are incompletely understood but evidence indicates that the deregulation o...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846721/ https://www.ncbi.nlm.nih.gov/pubmed/29529050 http://dx.doi.org/10.1371/journal.pone.0192963 |
_version_ | 1783305613946650624 |
---|---|
author | Valero-Jiménez, Ana Zúñiga, Joaquín Cisneros, José Becerril, Carina Salgado, Alfonso Checa, Marco Buendía-Roldán, Ivette Mendoza-Milla, Criselda Gaxiola, Miguel Pardo, Annie Selman, Moisés |
author_facet | Valero-Jiménez, Ana Zúñiga, Joaquín Cisneros, José Becerril, Carina Salgado, Alfonso Checa, Marco Buendía-Roldán, Ivette Mendoza-Milla, Criselda Gaxiola, Miguel Pardo, Annie Selman, Moisés |
author_sort | Valero-Jiménez, Ana |
collection | PubMed |
description | Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease characterized by epithelial cell activation, expansion of the fibroblast population and excessive extracellular matrix accumulation. The mechanisms are incompletely understood but evidence indicates that the deregulation of several proteases contributes to its pathogenesis. Transmembrane protease serine 4 (TMPRSS4) is a novel type II transmembrane serine protease that may promote migration and facilitate epithelial to mesenchymal transition (EMT), two critical processes in the pathogenesis of IPF. Thus, we hypothesized that over-expression of TMPRSS4 in the lung could promote the initiation and/or progression of IPF. In this study we first evaluated the expression and localization of TMPRSS4 in IPF lungs by real time PCR, western blot and immunohistochemistry. Then we examined the lung fibrotic response in wild-type and TMPRSS4 deficient mice using the bleomycin-induced lung injury model. We found that this protease is upregulated in IPF lungs, where was primarily expressed by epithelial and mast cells. Paralleling the findings in vivo, TMPRSS4 was expressed by alveolar and bronchial epithelial cells in vitro and unexpectedly, provoked an increase of E-cadherin. No expression was observed in normal human or IPF lung fibroblasts. The lung fibrotic response evaluated at 28 days after bleomycin injury was markedly attenuated in the haplodeficient and deficient TMPRSS4 mice. By morphology, a significant reduction of the fibrotic index was observed in KO and heterozygous mice which was confirmed by measurement of collagen content (hydroxyproline: WT: 164±21.1 μg/lung versus TMPRSS4 haploinsufficient: 110.2±14.3 μg/lung and TMPRSS4 deficient mice: 114.1±24.2 μg/lung (p<0.01). As in IPF, TMPRSS4 was also expressed in epithelial and mast cells. These findings indicate that TMPRSS4 is upregulated in IPF lungs and that may have a profibrotic role. |
format | Online Article Text |
id | pubmed-5846721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58467212018-03-23 Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury Valero-Jiménez, Ana Zúñiga, Joaquín Cisneros, José Becerril, Carina Salgado, Alfonso Checa, Marco Buendía-Roldán, Ivette Mendoza-Milla, Criselda Gaxiola, Miguel Pardo, Annie Selman, Moisés PLoS One Research Article Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease characterized by epithelial cell activation, expansion of the fibroblast population and excessive extracellular matrix accumulation. The mechanisms are incompletely understood but evidence indicates that the deregulation of several proteases contributes to its pathogenesis. Transmembrane protease serine 4 (TMPRSS4) is a novel type II transmembrane serine protease that may promote migration and facilitate epithelial to mesenchymal transition (EMT), two critical processes in the pathogenesis of IPF. Thus, we hypothesized that over-expression of TMPRSS4 in the lung could promote the initiation and/or progression of IPF. In this study we first evaluated the expression and localization of TMPRSS4 in IPF lungs by real time PCR, western blot and immunohistochemistry. Then we examined the lung fibrotic response in wild-type and TMPRSS4 deficient mice using the bleomycin-induced lung injury model. We found that this protease is upregulated in IPF lungs, where was primarily expressed by epithelial and mast cells. Paralleling the findings in vivo, TMPRSS4 was expressed by alveolar and bronchial epithelial cells in vitro and unexpectedly, provoked an increase of E-cadherin. No expression was observed in normal human or IPF lung fibroblasts. The lung fibrotic response evaluated at 28 days after bleomycin injury was markedly attenuated in the haplodeficient and deficient TMPRSS4 mice. By morphology, a significant reduction of the fibrotic index was observed in KO and heterozygous mice which was confirmed by measurement of collagen content (hydroxyproline: WT: 164±21.1 μg/lung versus TMPRSS4 haploinsufficient: 110.2±14.3 μg/lung and TMPRSS4 deficient mice: 114.1±24.2 μg/lung (p<0.01). As in IPF, TMPRSS4 was also expressed in epithelial and mast cells. These findings indicate that TMPRSS4 is upregulated in IPF lungs and that may have a profibrotic role. Public Library of Science 2018-03-12 /pmc/articles/PMC5846721/ /pubmed/29529050 http://dx.doi.org/10.1371/journal.pone.0192963 Text en © 2018 Valero-Jiménez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Valero-Jiménez, Ana Zúñiga, Joaquín Cisneros, José Becerril, Carina Salgado, Alfonso Checa, Marco Buendía-Roldán, Ivette Mendoza-Milla, Criselda Gaxiola, Miguel Pardo, Annie Selman, Moisés Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title | Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title_full | Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title_fullStr | Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title_full_unstemmed | Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title_short | Transmembrane protease, serine 4 (TMPRSS4) is upregulated in IPF lungs and increases the fibrotic response in bleomycin-induced lung injury |
title_sort | transmembrane protease, serine 4 (tmprss4) is upregulated in ipf lungs and increases the fibrotic response in bleomycin-induced lung injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846721/ https://www.ncbi.nlm.nih.gov/pubmed/29529050 http://dx.doi.org/10.1371/journal.pone.0192963 |
work_keys_str_mv | AT valerojimenezana transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT zunigajoaquin transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT cisnerosjose transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT becerrilcarina transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT salgadoalfonso transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT checamarco transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT buendiaroldanivette transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT mendozamillacriselda transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT gaxiolamiguel transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT pardoannie transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury AT selmanmoises transmembraneproteaseserine4tmprss4isupregulatedinipflungsandincreasesthefibroticresponseinbleomycininducedlunginjury |