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Herpesvirus-Mediated Delivery of a Genetically Encoded Fluorescent Ca(2+) Sensor to Canine Cardiomyocytes

We report the development and application of a pseudorabies virus-based system for delivery of troponeon, a fluorescent Ca(2+) sensor to adult canine cardiomyocytes. The efficacy of transduction was assessed by calculating the ratio of fluorescently labelled and nonlabelled cells in cell culture. In...

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Detalles Bibliográficos
Autores principales: Prorok, János, Kovács, Péter P., Kristóf, Attila A., Nagy, Norbert, Tombácz, Dóra, Tóth, Judit S., Ördög, Balázs, Jost, Norbert, Virág, László, Papp, Julius G., Varró, András, Tóth, András, Boldogkői, Zsolt
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712641/
https://www.ncbi.nlm.nih.gov/pubmed/19636419
http://dx.doi.org/10.1155/2009/361795
Descripción
Sumario:We report the development and application of a pseudorabies virus-based system for delivery of troponeon, a fluorescent Ca(2+) sensor to adult canine cardiomyocytes. The efficacy of transduction was assessed by calculating the ratio of fluorescently labelled and nonlabelled cells in cell culture. Interaction of the virus vector with electrophysiological properties of cardiomyocytes was evaluated by the analysis of transient outward current (I(to)), kinetics of the intracellular Ca(2+) transients, and cell shortening. Functionality of transferred troponeon was verified by FRET analysis. We demonstrated that the transfer efficiency of troponeon to cultured adult cardiac myocytes was virtually 100%. We showed that even after four days neither the amplitude nor the kinetics of the I(to) current was significantly changed and no major shifts occurred in parameters of [Ca(2+)](i) transients. Furthermore, we demonstrated that infection of cardiomyocytes with the virus did not affect the morphology, viability, and physiological attributes of cells.