## Abstract Embryonic stem (ES) cells proliferate and maintain their pluripotency for over 1 year in vitro and may therefore provide a sufficient source for cell therapies. However, most of the previously reported methods for obtaining a source for cell therapies have not been simple. We describe h
Viral transgenesis of embryonic cell cultures from the freshwater microcrustaceandaphnia
โ Scribed by Robinson, Christy D. ;Lourido, Sebastian ;Whelan, Sean P. ;Dudycha, Jeffry L. ;Lynch, Michael ;Isern, Sharon
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 199 KB
- Volume
- 305A
- Category
- Article
- ISSN
- 1548-8969
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โฆ Synopsis
The aim of this study was to determine whether a recombinant vesicular stomatitis virus (VSV) vector encoding a transgene could be used to infect and express a foreign gene in embryonic primary cell cultures derived from the freshwater microcrustacean Daphnia, the most widely used ecotoxicological model organism. To facilitate the evaluation of gene transfer, a reproducible method for establishing primary cultures from Daphnia embryonic tissues was developed. Within 24 hr after infection, transgene expression could be detected in cell culture. VSV was found to replicate in the cells with no apparent cytopathic effect. Here we report the first evidence of gene transfer and foreign gene expression in cultures of Daphnia embryonic cells using a recombinant viral vector.
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