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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/116738
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dc.contributor.authorFabro, Alexandre Todorovic-
dc.contributor.authorMinatel, Igor Otavio-
dc.contributor.authorRangel, Maristela Peres-
dc.contributor.authorHalbwedl, Iris-
dc.contributor.authorParra, Edwin Roger-
dc.contributor.authorCapelozzi, Vera Luiza-
dc.contributor.authorPopper, Helmut-
dc.date.accessioned2015-03-18T15:54:02Z-
dc.date.accessioned2016-10-25T20:27:57Z-
dc.date.available2015-03-18T15:54:02Z-
dc.date.available2016-10-25T20:27:57Z-
dc.date.issued2014-09-01-
dc.identifierhttp://dx.doi.org/10.1016/j.rmed.2014.06.008-
dc.identifier.citationRespiratory Medicine. London: W B Saunders Co Ltd, v. 108, n. 9, p. 1377-1386, 2014.-
dc.identifier.issn0954-6111-
dc.identifier.urihttp://hdl.handle.net/11449/116738-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/116738-
dc.description.abstractBackground: 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.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent1377-1386-
dc.language.isoeng-
dc.publisherW B Saunders Co Ltd-
dc.sourceWeb of Science-
dc.subjectEpithelial-mesenchymal transitionen
dc.subjectUsual interstitial pneumoniaen
dc.subjectIdiopathic pulmonary fibrosisen
dc.subjectSmoking-related interstitial fibrosisen
dc.subjectDouble-staining immunohistochemistryen
dc.titleUsual interstitial pneumonia and smoking-related interstitial fibrosis display epithelial to mesenchymal transition in fibroblastic focien
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionMed Univ Graz-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationSao Paulo State Univ, Botucatu Med Sch, Dept Pathol, Botucatu, SP, Brazil-
dc.description.affiliationMed Univ Graz, Inst Pathol, Graz, Austria-
dc.description.affiliationUniv Sao Paulo, Fac Med, Dept Pathol, Sao Paulo, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu Med Sch, Dept Pathol, Botucatu, SP, Brazil-
dc.description.sponsorshipIdCAPES: 2329-10-7-
dc.identifier.doi10.1016/j.rmed.2014.06.008-
dc.identifier.wosWOS:000342879200017-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofRespiratory Medicine-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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