期刊
PHYSIOLOGICAL GENOMICS
卷 12, 期 3, 页码 221-228出版社
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.00135.2002
关键词
cardiomyocytes; in vivo gene delivery; neurons; retina; transfection
资金
- NEI NIH HHS [EY-07132, R01 EY011388-06, EY-08571, EY-11388, R01 EY011388] Funding Source: Medline
- NHLBI NIH HHS [HL-33610, HL-56921] Funding Source: Medline
The aim of this study was to develop an efficient method for packaging and concentrating lentiviral vectors that consistently yields high-titer virus on a scale suitable for in vivo applications. Transient cotransfection of 293T packaging cells with DNA plasmids encoding lentiviral vector components was optimized using SuperFect, an activated dendrimer-based transfection reagent. The use of SuperFect allowed reproducible and efficient production of high-titer lentiviral vector at concentrations greater than 1 x 10(7) transducing units per ml (TU/ml) and required less than one-third of the total amount of DNA used in traditional calcium phosphate transfection methods. Viral titers were further increased using a novel concentration protocol that yielded an average final titer of 1.4 x 10(10) TU/ml. Lentiviruses produced using these methods exhibited efficient transduction of central nervous system and peripheral tissues in vivo. The method is reproducible and can be scaled up to facilitate the use of these vectors in animal studies.
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