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- W2592494573 abstract "Idiopathic pulmonary fibrosis (IPF) is a very common interstitial lung disease derived from chronic inflammatory insults, characterized by massive scar tissue deposition which causes the progressive loss of lung function and subsequent death for respiratory failure. Bleomycin is used as the standard agent to induce experimental pulmonary fibrosis in animal models for the study of its pathogenesis. However, to visualize the establishment of lung fibrosis after treatment, the animal sacrifice is necessary. Thus, the aim of this study was to avoid this limitation by using an innovative approach based on a double bleomycin treatment protocol, along with the in vivo images analysis of bleomycin treated mice. A reporter gene construct, containing the luciferase open reading frame under the matrix metalloproteinase-1 (MMP-1) promoter control region, was tested on double bleomycin-treated mice to investigate, in real time, the correlation between bleomycin treatment, inflammation, tissue remodeling and fibrosis. Bioluminescence emitted by the lungs of bleomycin treated mice, corroborated by Fluorescent Molecular Tomography (FMT), successfully allowed real time monitoring of fibrosis establishment. The reporter gene technology experienced in this work, could represents an advanced functional approach for real time noninvasive assessment of disease evolution during therapy, in a reliable and translational living animal model." @default.
- W2592494573 created "2017-03-16" @default.
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- W2592494573 date "2017-03-01" @default.
- W2592494573 modified "2023-09-26" @default.
- W2592494573 title "Heterologous Matrix Metalloproteinase Gene Promoter Activity Allows In Vivo Real-time Imaging of Bleomycin-Induced Lung Fibrosis in Transiently Transgenized Mice" @default.
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- W2592494573 doi "https://doi.org/10.3389/fimmu.2017.00199" @default.
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