Please use this identifier to cite or link to this item:
http://acervodigital.unesp.br/handle/11449/116738
- Title:
- Usual interstitial pneumonia and smoking-related interstitial fibrosis display epithelial to mesenchymal transition in fibroblastic foci
- Universidade Estadual Paulista (UNESP)
- Med Univ Graz
- Universidade de São Paulo (USP)
- 0954-6111
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
- CAPES: 2329-10-7
- 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.
- 1-Sep-2014
- Respiratory Medicine. London: W B Saunders Co Ltd, v. 108, n. 9, p. 1377-1386, 2014.
- 1377-1386
- W B Saunders Co Ltd
- Epithelial-mesenchymal transition
- Usual interstitial pneumonia
- Idiopathic pulmonary fibrosis
- Smoking-related interstitial fibrosis
- Double-staining immunohistochemistry
- http://dx.doi.org/10.1016/j.rmed.2014.06.008
- Acesso restrito
- outro
- http://repositorio.unesp.br/handle/11449/116738
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