Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis

<p>Abstract</p> <p>Background</p> <p>An altered susceptibility of lung fibroblasts to Fas-induced apoptosis has been implicated in the pathogenesis of pulmonary fibrosis; however, the underlying mechanism is not completely understood. Here, we studied the susceptibility...

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Main Authors: Wiesner Olaf, Röcken Christoph, Wille Aline, Bühling Frank, Baier Anja, Meinecke Ingmar, Welte Tobias, Pap Thomas
Format: Article
Language:English
Published: BMC 2005-04-01
Series:Respiratory Research
Online Access:http://respiratory-research.com/content/6/1/37
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author Wiesner Olaf
Röcken Christoph
Wille Aline
Bühling Frank
Baier Anja
Meinecke Ingmar
Welte Tobias
Pap Thomas
author_facet Wiesner Olaf
Röcken Christoph
Wille Aline
Bühling Frank
Baier Anja
Meinecke Ingmar
Welte Tobias
Pap Thomas
author_sort Wiesner Olaf
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>An altered susceptibility of lung fibroblasts to Fas-induced apoptosis has been implicated in the pathogenesis of pulmonary fibrosis; however, the underlying mechanism is not completely understood. Here, we studied the susceptibility of lung fibroblasts, obtained from patients with (f-fibs) and without pulmonary fibrosis (n-fibs), to FasL- (CD95L/APO-1) induced apoptosis in relation to the expression and the amounts of membrane-bound and soluble Fas. We also analysed the effects of tumor necrosis factor-β on FasL-induced cell death.</p> <p>Methods</p> <p>Apoptosis was induced with recombinant human FasL, with and without prior stimulation of the fibroblasts with tumor necrosis factor-α and measured by a histone fragmentation assay and flow cytometry. The expression of Fas mRNA was determined by quantitative PCR. The expression of cell surface Fas was determined by flow cytometry, and that of soluble Fas (sFas) was determined by enzyme-linked immunosorbent assay.</p> <p>Results</p> <p>When compared to n-fibs, f-fibs were resistant to FasL-induced apoptosis, despite significantly higher levels of Fas mRNA. F-fibs showed lower expression of surface-bound Fas but higher levels of sFas. While TNF-α increased the susceptibility to FasL-induced apoptosis in n-fibs, it had no pro-apoptotic effect in f-fibs.</p> <p>Conclusions</p> <p>The data suggest that lower expression of surface Fas, but higher levels of apoptosis-inhibiting sFas, contribute to the resistance of fibroblasts in lung fibrosis against apoptosis, to increased cellularity and also to increased formation and deposition of extracellular matrix.</p>
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spelling doaj.art-40ab04424ab846948f42c845b7d4d6492022-12-22T00:09:16ZengBMCRespiratory Research1465-99212005-04-01613710.1186/1465-9921-6-37Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosisWiesner OlafRöcken ChristophWille AlineBühling FrankBaier AnjaMeinecke IngmarWelte TobiasPap Thomas<p>Abstract</p> <p>Background</p> <p>An altered susceptibility of lung fibroblasts to Fas-induced apoptosis has been implicated in the pathogenesis of pulmonary fibrosis; however, the underlying mechanism is not completely understood. Here, we studied the susceptibility of lung fibroblasts, obtained from patients with (f-fibs) and without pulmonary fibrosis (n-fibs), to FasL- (CD95L/APO-1) induced apoptosis in relation to the expression and the amounts of membrane-bound and soluble Fas. We also analysed the effects of tumor necrosis factor-β on FasL-induced cell death.</p> <p>Methods</p> <p>Apoptosis was induced with recombinant human FasL, with and without prior stimulation of the fibroblasts with tumor necrosis factor-α and measured by a histone fragmentation assay and flow cytometry. The expression of Fas mRNA was determined by quantitative PCR. The expression of cell surface Fas was determined by flow cytometry, and that of soluble Fas (sFas) was determined by enzyme-linked immunosorbent assay.</p> <p>Results</p> <p>When compared to n-fibs, f-fibs were resistant to FasL-induced apoptosis, despite significantly higher levels of Fas mRNA. F-fibs showed lower expression of surface-bound Fas but higher levels of sFas. While TNF-α increased the susceptibility to FasL-induced apoptosis in n-fibs, it had no pro-apoptotic effect in f-fibs.</p> <p>Conclusions</p> <p>The data suggest that lower expression of surface Fas, but higher levels of apoptosis-inhibiting sFas, contribute to the resistance of fibroblasts in lung fibrosis against apoptosis, to increased cellularity and also to increased formation and deposition of extracellular matrix.</p>http://respiratory-research.com/content/6/1/37
spellingShingle Wiesner Olaf
Röcken Christoph
Wille Aline
Bühling Frank
Baier Anja
Meinecke Ingmar
Welte Tobias
Pap Thomas
Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
Respiratory Research
title Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
title_full Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
title_fullStr Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
title_full_unstemmed Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
title_short Altered expression of membrane-bound and soluble CD95/Fas contributes to the resistance of fibrotic lung fibroblasts to FasL induced apoptosis
title_sort altered expression of membrane bound and soluble cd95 fas contributes to the resistance of fibrotic lung fibroblasts to fasl induced apoptosis
url http://respiratory-research.com/content/6/1/37
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