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• W2043918650 abstract "Animal imaging requires the use of reliable long-term fluorescence methods and technology. The application of confocal imaging to in vivo monitoring of transgene expression within internal organs and tissues has been limited by the accessibility to these sites. We aimed to test the feasibility of fibred confocal fluorescence microscopy (FCFM) to image in situ green fluorescent protein (GFP) in cells of living animals. We used transgenic rabbits expressing the enhanced GFP (eGFP) gene. Detailed tissue architecture and cell morphology were visualised and identified in situ by FCFM. Imaging of vasculature by using FCFM revealed a single blood vessel or vasculature network. We also used non-transgenic female rabbits mated with transgenic males to visualise eGFP expression in extra-foetal membranes and the placenta. Expression of the eGFP gene was confirmed by FCFM. This new imaging technology offers specific characteristics: a way to gain access to organs and tissues in vivo, sensitive detection of fluorescent signals, and cellular observations with rapid acquisition at near real time. It allows an accurate visualisation of tissue anatomical structure and cell morphology. FCFM is a promising technology to study biological processes in the natural physiological environment of living animals." @default.
• W2043918650 created "2016-06-24" @default.
• W2043918650 creator A5039010213 @default.
• W2043918650 creator A5053110084 @default.
• W2043918650 date "2006-08-01" @default.
• W2043918650 modified "2023-10-17" @default.
• W2043918650 title "In vivo imaging of green fluorescent protein-expressing cells in transgenic animals using fibred confocal fluorescence microscopy" @default.
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• W2043918650 doi "https://doi.org/10.1016/j.ejcb.2006.03.007" @default.
• W2043918650 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16781011" @default.
• W2043918650 hasPublicationYear "2006" @default.
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