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Micro-computed tomography of pulmonary fibrosis in mice induced by adenoviral gene transfer of biologically active transforming growth factor-beta 1

 
: Rodt, T.; Falck, C. von; Dettmer, S.; Halter, R.; Maus, R.; Ask, K.; Kolb, M.; Gauldie, J.; Länger, F.; Hoy, L.; Welte, T.; Galanski, M.; Maus, U.A.; Borlak, J.

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Fulltext urn:nbn:de:0011-n-1571758 (741 KByte PDF)
MD5 Fingerprint: ae46112d7781bf155495ee769be98f53
Created on: 7.4.2011


Respiratory research. Online journal 11 (2010), Art. 181, 8 pp.
http://respiratory-research.com/
ISSN: 1465-993X
ISSN: 1465-9921
English
Journal Article, Electronic Publication
Fraunhofer ITEM ()

Abstract
BACKGROUND: Micro-computed tomography (micro-CT) is a novel tool for monitoring acute and chronic disease states in small laboratory animals. Its value for assessing progressive lung fibrosis in mice has not been reported so far. Here we examined the importance of in vivo micro-CT as non-invasive tool to assess progression of pulmonary fibrosis in mice over time.
METHODS: Pulmonary fibrosis was induced in mice by intratracheal delivery of an adenoviral gene vector encoding biologically active TGF-beta1 (AdTGF-beta1). Respiratory gated and ungated micro-CT scans were performed at 1, 2, 3, and 4 weeks post pulmonary adenoviral gene or control vector delivery, and were then correlated with respective histopathology-based Ashcroft scoring of pulmonary fibrosis in mice. Visual assessment of image quality and consolidation was performed by 3 observers and a semi-automated quantification algorithm was applied to quantify aerated pulmonary volume as an inverse surrogate marker for pulmonary fibrosis.
RESULTS: We found a significant correlation between classical Ashcroft scoring and micro-CT assessment using both visual assessment and the semi-automated quantification algorithm. Pulmonary fibrosis could be clearly detected in micro-CT, image quality values were higher for respiratory gated exams, although differences were not significant. For assessment of fibrosis no significant difference between respiratory gated and ungated exams was observed.
CONCLUSIONS: Together, we show that micro-CT is a powerful tool to assess pulmonary fibrosis in mice, using both visual assessment and semi-automated quantification algorithms. These data may be important in view of pre-clinical pharmacologic interventions for the treatment of lung fibrosis in small laboratory animals.

: http://publica.fraunhofer.de/documents/N-157175.html