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New transgenic NIS reporter rats for longitudinal tracking of fibrogenesis by high-resolution imaging.
- Source :
-
Scientific reports [Sci Rep] 2018 Sep 21; Vol. 8 (1), pp. 14209. Date of Electronic Publication: 2018 Sep 21. - Publication Year :
- 2018
-
Abstract
- Fibrogenesis is the underlying mechanism of wound healing and repair. Animal models that enable longitudinal monitoring of fibrogenesis are needed to improve traditional tissue analysis post-mortem. Here, we generated transgenic reporter rats expressing the sodium iodide symporter (NIS) driven by the rat collagen type-1 alpha-1 (Col1α1) promoter and demonstrated that fibrogenesis can be visualized over time using SPECT or PET imaging following activation of NIS expression by rotator cuff (RC) injury. Radiotracer uptake was first detected in and around the injury site day 3 following surgery, increasing through day 7-14, and declining by day 21, revealing for the first time, the kinetics of Col1α1 promoter activity in situ. Differences in the intensity and duration of NIS expression/collagen promoter activation between individual RC injured Col1α1-hNIS rats were evident. Dexamethasone treatment delayed time to peak NIS signals, showing that modulation of fibrogenesis by a steroid can be imaged with exquisite sensitivity and resolution in living animals. NIS reporter rats would facilitate studies in physiological wound repair and pathological processes such as fibrosis and the development of anti-fibrotic drugs.
- Subjects :
- Animals
Collagen Type I genetics
Collagen Type I, alpha 1 Chain
DNA, Complementary genetics
Female
Fibrosis genetics
Humans
Positron-Emission Tomography methods
Promoter Regions, Genetic genetics
Rats
Rats, Transgenic
Tomography, Emission-Computed, Single-Photon methods
Wound Healing genetics
Genes, Reporter genetics
Symporters genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 8
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 30242176
- Full Text :
- https://doi.org/10.1038/s41598-018-32442-x