Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/21105
Appears in Collections:Biological and Environmental Sciences Journal Articles
Peer Review Status: Refereed
Title: Enhanced nanomagnetic gene transfection of human prenatal cardiac progenitor cells and adult cardiomyocytes
Author(s): Subramanian, Mahendran
Lim, Jenson
Dobson, John
Contact Email: jenson.lim@stir.ac.uk
Issue Date: 31-Jul-2013
Date Deposited: 22-Sep-2014
Citation: Subramanian M, Lim J & Dobson J (2013) Enhanced nanomagnetic gene transfection of human prenatal cardiac progenitor cells and adult cardiomyocytes. PLoS ONE, 8 (7), Art. No.: e69812. https://doi.org/10.1371/journal.pone.0069812
Abstract: Magnetic nanoparticle-based gene transfection has been shown to be an effective, non-viral technique for delivery of both plasmid DNA and siRNA into cells in culture. It has several advantages over other non-viral delivery techniques, such as short transfection times and high cell viability. These advantages have been demonstrated in a number of primary cells and cell lines. Here we report that oscillating magnet array-based nanomagnetic transfection significantly improves transfection efficiency in both human prenatal cardiac progenitor cells and adult cardiomyocytes when compared to static magnetofection, cationic lipid reagents and electroporation, while maintaining high cell viability. In addition, transfection of adult cardiomyocytes was improved further by seeding the cells onto Collagen I-coated plates, with transfection efficiencies of up to 49% compared to 24% with lipid reagents and 19% with electroporation. These results demonstrate that oscillating nanomagnetic transfection far outperforms other non-viral transfection techniques in these important cells.
DOI Link: 10.1371/journal.pone.0069812
Rights: © 2013 Subramanian et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Licence URL(s): http://creativecommons.org/licenses/by/3.0/

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