Cargando…

Altered fibroblast proteoglycan production in COPD

BACKGROUND: Airway remodeling in COPD includes reorganization of the extracellular matrix. Proteoglycans play a crucial role in this process as regulators of the integrity of the extracellular matrix. Altered proteoglycan immunostaining has been demonstrated in COPD lungs and this has been suggested...

Descripción completa

Detalles Bibliográficos
Autores principales: Hallgren, Oskar, Nihlberg, Kristian, Dahlbäck, Magnus, Bjermer, Leif, Eriksson, Leif T, Erjefält, Jonas S, Löfdahl, Claes-Göran, Westergren-Thorsson, Gunilla
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2886021/
https://www.ncbi.nlm.nih.gov/pubmed/20459817
http://dx.doi.org/10.1186/1465-9921-11-55
_version_ 1782182426719551488
author Hallgren, Oskar
Nihlberg, Kristian
Dahlbäck, Magnus
Bjermer, Leif
Eriksson, Leif T
Erjefält, Jonas S
Löfdahl, Claes-Göran
Westergren-Thorsson, Gunilla
author_facet Hallgren, Oskar
Nihlberg, Kristian
Dahlbäck, Magnus
Bjermer, Leif
Eriksson, Leif T
Erjefält, Jonas S
Löfdahl, Claes-Göran
Westergren-Thorsson, Gunilla
author_sort Hallgren, Oskar
collection PubMed
description BACKGROUND: Airway remodeling in COPD includes reorganization of the extracellular matrix. Proteoglycans play a crucial role in this process as regulators of the integrity of the extracellular matrix. Altered proteoglycan immunostaining has been demonstrated in COPD lungs and this has been suggested to contribute to the pathogenesis. The major cell type responsible for production and maintenance of ECM constituents, such as proteoglycans, are fibroblasts. Interestingly, it has been proposed that central airways and alveolar lung parenchyma contain distinct fibroblast populations. This study explores the hypothesis that altered depositions of proteoglycans in COPD lungs, and in particular versican and perlecan, is a result of dysregulated fibroblast proteoglycan production. METHODS: Proliferation, proteoglycan production and the response to TGF-β(1 )were examined in vitro in centrally and distally derived fibroblasts isolated from COPD patients (GOLD stage IV) and from control subjects. RESULTS: Phenotypically different fibroblast populations were identified in central airways and in the lung parenchyma. Versican production was higher in distal fibroblasts from COPD patients than from control subjects (p < 0.01). In addition, perlecan production was lower in centrally derived fibroblasts from COPD patients than from control subjects (p < 0.01). TGF-β(1 )triggered similar increases in proteoglycan production in distally derived fibroblasts from COPD patients and control subjects. In contrast, centrally derived fibroblasts from COPD patients were less responsive to TGF-β(1 )than those from control subjects. CONCLUSIONS: The results show that fibroblasts from COPD patients have alterations in proteoglycan production that may contribute to disease development. Distally derived fibroblasts from COPD patients have enhanced production of versican that may have a negative influence on the elastic recoil. In addition, a lower perlecan production in centrally derived fibroblasts from COPD patients may indicate alterations in bronchial basement membrane integrity in severe COPD.
format Text
id pubmed-2886021
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28860212010-06-16 Altered fibroblast proteoglycan production in COPD Hallgren, Oskar Nihlberg, Kristian Dahlbäck, Magnus Bjermer, Leif Eriksson, Leif T Erjefält, Jonas S Löfdahl, Claes-Göran Westergren-Thorsson, Gunilla Respir Res Research BACKGROUND: Airway remodeling in COPD includes reorganization of the extracellular matrix. Proteoglycans play a crucial role in this process as regulators of the integrity of the extracellular matrix. Altered proteoglycan immunostaining has been demonstrated in COPD lungs and this has been suggested to contribute to the pathogenesis. The major cell type responsible for production and maintenance of ECM constituents, such as proteoglycans, are fibroblasts. Interestingly, it has been proposed that central airways and alveolar lung parenchyma contain distinct fibroblast populations. This study explores the hypothesis that altered depositions of proteoglycans in COPD lungs, and in particular versican and perlecan, is a result of dysregulated fibroblast proteoglycan production. METHODS: Proliferation, proteoglycan production and the response to TGF-β(1 )were examined in vitro in centrally and distally derived fibroblasts isolated from COPD patients (GOLD stage IV) and from control subjects. RESULTS: Phenotypically different fibroblast populations were identified in central airways and in the lung parenchyma. Versican production was higher in distal fibroblasts from COPD patients than from control subjects (p < 0.01). In addition, perlecan production was lower in centrally derived fibroblasts from COPD patients than from control subjects (p < 0.01). TGF-β(1 )triggered similar increases in proteoglycan production in distally derived fibroblasts from COPD patients and control subjects. In contrast, centrally derived fibroblasts from COPD patients were less responsive to TGF-β(1 )than those from control subjects. CONCLUSIONS: The results show that fibroblasts from COPD patients have alterations in proteoglycan production that may contribute to disease development. Distally derived fibroblasts from COPD patients have enhanced production of versican that may have a negative influence on the elastic recoil. In addition, a lower perlecan production in centrally derived fibroblasts from COPD patients may indicate alterations in bronchial basement membrane integrity in severe COPD. BioMed Central 2010 2010-05-11 /pmc/articles/PMC2886021/ /pubmed/20459817 http://dx.doi.org/10.1186/1465-9921-11-55 Text en Copyright ©2010 Hallgren 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
Hallgren, Oskar
Nihlberg, Kristian
Dahlbäck, Magnus
Bjermer, Leif
Eriksson, Leif T
Erjefält, Jonas S
Löfdahl, Claes-Göran
Westergren-Thorsson, Gunilla
Altered fibroblast proteoglycan production in COPD
title Altered fibroblast proteoglycan production in COPD
title_full Altered fibroblast proteoglycan production in COPD
title_fullStr Altered fibroblast proteoglycan production in COPD
title_full_unstemmed Altered fibroblast proteoglycan production in COPD
title_short Altered fibroblast proteoglycan production in COPD
title_sort altered fibroblast proteoglycan production in copd
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2886021/
https://www.ncbi.nlm.nih.gov/pubmed/20459817
http://dx.doi.org/10.1186/1465-9921-11-55
work_keys_str_mv AT hallgrenoskar alteredfibroblastproteoglycanproductionincopd
AT nihlbergkristian alteredfibroblastproteoglycanproductionincopd
AT dahlbackmagnus alteredfibroblastproteoglycanproductionincopd
AT bjermerleif alteredfibroblastproteoglycanproductionincopd
AT erikssonleift alteredfibroblastproteoglycanproductionincopd
AT erjefaltjonass alteredfibroblastproteoglycanproductionincopd
AT lofdahlclaesgoran alteredfibroblastproteoglycanproductionincopd
AT westergrenthorssongunilla alteredfibroblastproteoglycanproductionincopd