Abstract
FRTL-5 cells are used in many laboratories as an in vitro system of thyroid follicular cells since they share many properties of human thyrocytes. However, the use of FRTL-5 cells for experimental modifications is limited by low transfection efficiencies of lipid-based transfections and the need for cumbersome viral transduction protocols. A new technology – nucleofection – has become available for cell lines that are difficult to transfect. Here, we report the application and optimization of this method in FRTL-5 cells. Using the green fluorescent protein (GFP) as a reporter gene, FRTL-5 cells were easily transfectable with efficiencies over 60%. In addition, the simultaneous transfer of siRNA against GFP was feasible and allowed suppression of GFP over at least 4 days. Furthermore nucleofection was successful for establishing stable FRTL-5 cell clones. In conclusion, this optimized fast and efficient nucleofection protocol offers new properties for the experimental use of FRTL-5 cells.
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Correspondence
D. FuhrerMD PhD
Department of Internal Medicine
Division of Endocrinology and Nephrology
University of Leipzig
Liebigstraße 18
04103 Leipzig
Telefon: +49/341/971 3301
Fax: +49/341/971 3389
eMail: Dagmar.Fuehrer@medizin.uni-leipzig.de