Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease

<p>Abstract</p> <p>Background</p> <p>The reticular basement membrane (Rbm) in smokers and especially smokers with COPD is fragmented with "clefts" containing cells staining for the collagenase matrix-metalloproteinase-9 (MMP-9) and fibroblast protein, S100A4....

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Main Authors: Wood-Baker Richard, Muller H Konrad, Weston Steven, Ward Chris, Soltani Amir, Reid David, Sohal Sukhwinder S, Walters E Haydn
Format: Article
Language:English
Published: BMC 2011-10-01
Series:Respiratory Research
Subjects:
Online Access:http://respiratory-research.com/content/12/1/130
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spelling doaj-98f9516f4d3b4a71826270089ab2a1be2020-11-24T21:36:18ZengBMCRespiratory Research1465-99212011-10-0112113010.1186/1465-9921-12-130Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary diseaseWood-Baker RichardMuller H KonradWeston StevenWard ChrisSoltani AmirReid DavidSohal Sukhwinder SWalters E Haydn<p>Abstract</p> <p>Background</p> <p>The reticular basement membrane (Rbm) in smokers and especially smokers with COPD is fragmented with "clefts" containing cells staining for the collagenase matrix-metalloproteinase-9 (MMP-9) and fibroblast protein, S100A4. These cells are also present in the basal epithelium. Such changes are likely hallmarks of epithelial mesenchymal transition (EMT). We aimed to confirm the epithelial origin of these Rbm cells, and to exclude potential confounding by infiltrating inflammatory cells.</p> <p>Methods</p> <p>Endobronchial biopsy sections from 17 COPD current smokers, with documented Rbm splitting and cellularity were stained for neutrophil elastase (neutrophil marker), CD68 (macrophage/mature fibroblasts), CD4+/CD8+ T lymphocytes, CD19 (B-cells), CD11c (dendritic cells/inflammatory cells), and S100 (Langerhans cells). The number of cells in the Rbm and epithelium staining for these "inflammatory" cell markers were then compared to numbers staining for S100A4, "a documented EMT epitope". Slides were double stained for S100A4 and cytokeratin(s).</p> <p>Results</p> <p>In the basal epithelium significantly more cells stained for S100A4 compared to infiltrating macrophages, fibroblasts or immune cells: median, 26 (21.3 - 37.3) versus 0 (0 - 9.6) per mm, p < 0.003. Markedly more S100A4 staining cells were also observed in the Rbm compared to infiltrating macrophages, neutrophils, fibroblasts or immune cells or any sub-type: 58 (37.3 - 92.6) versus 0 (0 - 4.8) cells/mm Rbm, p < 0.003. Cells in the basal epithelium 26 (21.3 - 37.3) per mm) and Rbm (5.9 (2.3 - 13.8) per mm) frequently double stained for both cytokeratin and S100A4.</p> <p>Conclusions</p> <p>These data provide additional support for active EMT in COPD airways.</p> http://respiratory-research.com/content/12/1/130cytokeratincleftsepithelial mesenchymal transition (EMT)inflammatory cells and S100A4
collection DOAJ
language English
format Article
sources DOAJ
author Wood-Baker Richard
Muller H Konrad
Weston Steven
Ward Chris
Soltani Amir
Reid David
Sohal Sukhwinder S
Walters E Haydn
spellingShingle Wood-Baker Richard
Muller H Konrad
Weston Steven
Ward Chris
Soltani Amir
Reid David
Sohal Sukhwinder S
Walters E Haydn
Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
Respiratory Research
cytokeratin
clefts
epithelial mesenchymal transition (EMT)
inflammatory cells and S100A4
author_facet Wood-Baker Richard
Muller H Konrad
Weston Steven
Ward Chris
Soltani Amir
Reid David
Sohal Sukhwinder S
Walters E Haydn
author_sort Wood-Baker Richard
title Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
title_short Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
title_full Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
title_fullStr Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
title_full_unstemmed Evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
title_sort evaluation of epithelial mesenchymal transition in patients with chronic obstructive pulmonary disease
publisher BMC
series Respiratory Research
issn 1465-9921
publishDate 2011-10-01
description <p>Abstract</p> <p>Background</p> <p>The reticular basement membrane (Rbm) in smokers and especially smokers with COPD is fragmented with "clefts" containing cells staining for the collagenase matrix-metalloproteinase-9 (MMP-9) and fibroblast protein, S100A4. These cells are also present in the basal epithelium. Such changes are likely hallmarks of epithelial mesenchymal transition (EMT). We aimed to confirm the epithelial origin of these Rbm cells, and to exclude potential confounding by infiltrating inflammatory cells.</p> <p>Methods</p> <p>Endobronchial biopsy sections from 17 COPD current smokers, with documented Rbm splitting and cellularity were stained for neutrophil elastase (neutrophil marker), CD68 (macrophage/mature fibroblasts), CD4+/CD8+ T lymphocytes, CD19 (B-cells), CD11c (dendritic cells/inflammatory cells), and S100 (Langerhans cells). The number of cells in the Rbm and epithelium staining for these "inflammatory" cell markers were then compared to numbers staining for S100A4, "a documented EMT epitope". Slides were double stained for S100A4 and cytokeratin(s).</p> <p>Results</p> <p>In the basal epithelium significantly more cells stained for S100A4 compared to infiltrating macrophages, fibroblasts or immune cells: median, 26 (21.3 - 37.3) versus 0 (0 - 9.6) per mm, p < 0.003. Markedly more S100A4 staining cells were also observed in the Rbm compared to infiltrating macrophages, neutrophils, fibroblasts or immune cells or any sub-type: 58 (37.3 - 92.6) versus 0 (0 - 4.8) cells/mm Rbm, p < 0.003. Cells in the basal epithelium 26 (21.3 - 37.3) per mm) and Rbm (5.9 (2.3 - 13.8) per mm) frequently double stained for both cytokeratin and S100A4.</p> <p>Conclusions</p> <p>These data provide additional support for active EMT in COPD airways.</p>
topic cytokeratin
clefts
epithelial mesenchymal transition (EMT)
inflammatory cells and S100A4
url http://respiratory-research.com/content/12/1/130
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