Novel Adenovirus Component System That Transfects Cultured Cardiac Cells With High Efficiency

• Published in: Circulation research 1996-06, Vol.78 (6), p.971-977
• Main Authors: Kohout, Trudy A, O'Brian, Jeffrey J, Gaa, Shirley T, Lederer, W. Jonathan, Rogers, Terry B
• Format: Article
• Language: English
• Subjects: Adenoviruses, Human - genetics; Animals; beta-Galactosidase - genetics; Biological and medical sciences; Cells, Cultured; Fundamental and applied biological sciences. Psychology; Heart; Humans; Myocardium - metabolism; Plasmids; Protein Kinase C; Rats; Rats, Sprague-Dawley; Transfection; Vertebrates: cardiovascular system
• ISSN: 0009-7330; 1524-4571
• DOI: 10.1161/01.RES.78.6.971

Although it is clear that gene transfection is a potentially valuable approach in the study of cardiac cell function and differentiation, classic transfection methods are limited by their poor efficiencies in cardiac cells. Recent studies show that recombinant replication-defective human adenovirus can transfect primary cardiac cultures with near 100% efficiency. Since such recombinants are time consuming to prepare, the goal of this study was to develop a plasmid/viral transfection system that would capitalize on the advantages of adenovirus. We have found that a ``component system'' formed by preincubation of Ad5dl312 adenovirus, poly-L-lysine, and an expression plasmid (lacZ reporter gene under control of the human cytomegalovirus (HCMV) major immediate early promoter) can transfect cultured cardiac cells. Optimal conditions were determined by quantifying beta-galactosidase expression. Histochemical analysis of cultures revealed that the component system transfected 70% of the cells under these conditions. LacZ-positive myocytes could be identified in intact myocytes with the fluorescent substrate C12-fluorescein di-beta-galactopyranoside. Functional studies with such cells indicated that contractile behavior was maintained in transfected cardiocytes. Furthermore, the component system was used to transfect a DNA vector expressing a physiologically relevant protein, protein kinase C delta. In summary, this powerful and simple approach can promote the expression of heterologous genes that can be studied at the biochemical and cellular level in cardiac cells.(Circ Res. 1996;78:971-977.)