Publicação: Usual interstitial pneumonia and smoking-related interstitial fibrosis display epithelial to mesenchymal transition in fibroblastic foci
dc.contributor.author | Fabro, Alexandre Todorovic [UNESP] | |
dc.contributor.author | Minatel, Igor Otavio [UNESP] | |
dc.contributor.author | Rangel, Maristela Peres | |
dc.contributor.author | Halbwedl, Iris | |
dc.contributor.author | Parra, Edwin Roger | |
dc.contributor.author | Capelozzi, Vera Luiza | |
dc.contributor.author | Popper, Helmut | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Med Univ Graz | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2015-03-18T15:54:02Z | |
dc.date.available | 2015-03-18T15:54:02Z | |
dc.date.issued | 2014-09-01 | |
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. | en |
dc.description.affiliation | Sao Paulo State Univ, Botucatu Med Sch, Dept Pathol, Botucatu, SP, Brazil | |
dc.description.affiliation | Med Univ Graz, Inst Pathol, Graz, Austria | |
dc.description.affiliation | Univ Sao Paulo, Fac Med, Dept Pathol, Sao Paulo, Brazil | |
dc.description.affiliationUnesp | Sao Paulo State Univ, Botucatu Med Sch, Dept Pathol, Botucatu, SP, Brazil | |
dc.description.sponsorship | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description.sponsorshipId | CAPES: 2329-10-7 | |
dc.format.extent | 1377-1386 | |
dc.identifier | http://dx.doi.org/10.1016/j.rmed.2014.06.008 | |
dc.identifier.citation | Respiratory Medicine. London: W B Saunders Co Ltd, v. 108, n. 9, p. 1377-1386, 2014. | |
dc.identifier.doi | 10.1016/j.rmed.2014.06.008 | |
dc.identifier.issn | 0954-6111 | |
dc.identifier.uri | http://hdl.handle.net/11449/116738 | |
dc.identifier.wos | WOS:000342879200017 | |
dc.language.iso | eng | |
dc.publisher | W B Saunders Co Ltd | |
dc.relation.ispartof | Respiratory Medicine | |
dc.relation.ispartofjcr | 3.230 | |
dc.relation.ispartofsjr | 1,472 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | Epithelial-mesenchymal transition | en |
dc.subject | Usual interstitial pneumonia | en |
dc.subject | Idiopathic pulmonary fibrosis | en |
dc.subject | Smoking-related interstitial fibrosis | en |
dc.subject | Double-staining immunohistochemistry | en |
dc.title | Usual interstitial pneumonia and smoking-related interstitial fibrosis display epithelial to mesenchymal transition in fibroblastic foci | en |
dc.type | Artigo | |
dcterms.rightsHolder | W B Saunders Co Ltd | |
dspace.entity.type | Publication | |
unesp.author.orcid | 0000-0002-7687-3161[1] | |
unesp.author.orcid | 0000-0002-9922-2871[2] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatu | pt |
unesp.department | Patologia - FMB | pt |