dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.contributor | Med Univ Graz | |
dc.contributor | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2015-03-18T15:54:02Z | |
dc.date.available | 2015-03-18T15:54:02Z | |
dc.date.created | 2015-03-18T15:54:02Z | |
dc.date.issued | 2014-09-01 | |
dc.identifier | Respiratory Medicine. London: W B Saunders Co Ltd, v. 108, n. 9, p. 1377-1386, 2014. | |
dc.identifier | 0954-6111 | |
dc.identifier | http://hdl.handle.net/11449/116738 | |
dc.identifier | 10.1016/j.rmed.2014.06.008 | |
dc.identifier | WOS:000342879200017 | |
dc.description.abstract | Background: Fibroblastic foci (FF) are a major histological feature of usual interstitial pneumonia (UIP) in idiopathic pulmonary fibrosis (IPF) and collagen vascular diseases (non-IPF). In addition, FF are occasionally associated with smoking-related interstitial fibrosis (SRIF). Recent studies have suggested a role for epithelial to mesenchymal transition (EMT) in pulmonary fibrogenesis.Methods: Here, we investigated whether EMT was present in patients with IPF (n = 19), non-IPF (n = 17), and SRIF (n = 16) using morphometric immunohistochemistry, electron microscopy, and confocal microscopy. All patients had received lung biopsies or lobectomies for lung cancer.Results: IPF and non-IPF patients displayed restrictive lung function patterns, whereas those with SRIF presented mixed patterns. Cells within FF presented high number of alpha-smooth muscle actin (alpha SMA)-staining cells; however, the foci of IPF patients showed comparatively lower number. Moreover, colocalization of thyroid transcription factor-1 (TTF1) and alpha SMA within FF showed low number of staining cells for IPF and SRIF in comparison to non-IPF (p < 0.01). Nevertheless, all groups displayed colocalization of high rate of TTF1(+)-cells and low rate of alpha SMA(+)-cells within hyperplastic epithelioid cells in FF. Also, we observed areas with low proportion of TTF1(+) cells and alpha SMA(+) cells, which were present in SRIF and non-IPF more often than IPF (p < 0.001). Electron microscopy revealed small breaks in the alveolar basal lamina, which allowed epithelioid cells to directly contact the collagenous matrix and fibroblasts. Three-dimensional reconstruction revealed intense alpha SMA staining within some epithelioid cells, suggesting that they had gained a mesenchymal phenotype.Conclusions: These findings constitute the first report of EMT in SRIF and suggest that EMT occurs more prominently in SRIF and non-IPF than IPF. (C) 2014 Elsevier Ltd. All rights reserved. | |
dc.language | eng | |
dc.publisher | W B Saunders Co Ltd | |
dc.relation | Respiratory Medicine | |
dc.relation | 3.230 | |
dc.relation | 1,472 | |
dc.rights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | Epithelial-mesenchymal transition | |
dc.subject | Usual interstitial pneumonia | |
dc.subject | Idiopathic pulmonary fibrosis | |
dc.subject | Smoking-related interstitial fibrosis | |
dc.subject | Double-staining immunohistochemistry | |
dc.title | Usual interstitial pneumonia and smoking-related interstitial fibrosis display epithelial to mesenchymal transition in fibroblastic foci | |
dc.type | Artículos de revistas | |