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Cell-cell electrofusion: optimization of electric field amplitude and hypotonic treatment for mouse melanoma (B16-F1) and Chinese Hamster ovary (CHO) cells.

Authors :
Ušaj, Marko
Trontelj, Katja
Miklavčič, Damijan
Kandušer, Masša
Usaj, Marko
Miklavcic, Damijan
Kanduser, Masa
Source :
Journal of Membrane Biology; Jul2010, Vol. 236 Issue 1, p107-116, 10p, 3 Diagrams, 4 Charts, 2 Graphs
Publication Year :
2010

Abstract

Efficient electroporation of cells in physical contact induces cell fusion, and this process is known as electrofusion. It has been shown that appropriate hypotonic treatment of cells before the application of electric pulses can cause a significant increase in electrofusion efficiency. First, the amplitudes of the electric field were determined spectrofluorometrically, where sufficient permeabilization in hypotonic buffer occurred for B16-F1 and CHO cells. In further electrofusion experiments 14 +/- 4% of fused cells for B16-F1 and 6 +/- 1% for CHO was achieved. These electrofusion efficiencies, determined by double staining and fluorescence microcopy, are comparable to those of other published studies. It was also confirmed that successful electroporation does not necessarily guarantee high electrofusion efficiency due to biological factors involved in the electrofusion process. Furthermore, not only the extension of electrofusion but also cell survival depends on the cell line used. Further studies are needed to improve overall cell survival after electroporation in hypotonic buffer, which was significantly reduced, especially for B16-F1 cells. Another contribution of this report is the description of a simple modification of the adherence method for formation of spontaneous cell contact, while cells preserve their spherical shape. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222631
Volume :
236
Issue :
1
Database :
Complementary Index
Journal :
Journal of Membrane Biology
Publication Type :
Academic Journal
Accession number :
52671273
Full Text :
https://doi.org/10.1007/s00232-010-9272-3