Optimization of transfection methods for Huh­7 and Vero cells: a comparative study

Availability of an efficient transfection protocol is the first determinant in success of gene transferring studies in mammalian cells which is accomplished experimentally for every single cell type. Herein, we provide data of a comparative study on optimization of transfection condition by electrop...

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Datum:2012
Hauptverfasser: Hashemi, A., Roohvand, F., Ghahremani, M.H., Aghasadeghi, M.R., Vahabpour, R., Motevali, F., Memarnejadian, A.
Format: Artikel
Sprache:English
Veröffentlicht: Інститут клітинної біології та генетичної інженерії НАН України 2012
Schriftenreihe:Цитология и генетика
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Online Zugang:http://dspace.nbuv.gov.ua/handle/123456789/126499
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Zitieren:Optimization of transfection methods for Huh­7 and Vero cells: a comparative study / A. Hashemi, F. Roohvand, M.H. Ghahremani, M.R. Aghasadeghi, R. Vahabpour, F. Motevali, A. Memarnejadian // Цитология и генетика. — 2012. — Т. 46, № 6. — С. 19-27. — Бібліогр.: 37 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Zusammenfassung:Availability of an efficient transfection protocol is the first determinant in success of gene transferring studies in mammalian cells which is accomplished experimentally for every single cell type. Herein, we provide data of a comparative study on optimization of transfection condition by electroporation and chemical methods for Huh-7 and Vero cells. Different cell confluencies, DNA/reagent ratios and total transfection volumes were optimized for two chemical reagents including jetPEI™ and Lipofectamine™ 2000. Besides, the effects of electric field strength and pulse length were investigated to improve electroporation efficiency. Transfection of cells by pEGFP-N1 vector and tracking the expression of GFP by FACS and Fluorescence Microscopy analysis were the employed methods to evaluate transfection efficiencies. Optimized electroporation protocols yielded 63.73 ± ± 2.36 and 73.9 ± 1.6 % of transfection in Huh-7 and Vero cells respectively, while maximum achieved level of transfection by jetPEI™ was respectively 14.2 ± 0.69 and 28 ± 1.11 % for the same cells. Post transfectional chilling of the cells did not improve electrotransfection efficiency of Huh-7 cells. Compared to chemical based reagents, electroporation showed the superior levels of transfection in both cell lines. The presented protocols should satisfy most of the experimental applications requiring high transfection efficiencies of these two cell lines.