共 24 条
Electroporation-mediated gene transfer directly to the swine heart
被引:28
作者:
Hargrave, B.
[1
,2
]
Downey, H.
[1
]
Strange, R., Jr.
[3
]
Murray, L.
[4
]
Cinnamond, C.
[3
]
Lundberg, C.
[1
]
Israel, A.
[1
]
Chen, Y-J
[1
]
Marshall, W., Jr.
[5
]
Heller, R.
[1
,6
]
机构:
[1] Old Dominion Univ, Frank Reidy Res Ctr Bioelect, Norfolk, VA 23508 USA
[2] Old Dominion Univ, Coll Sci, Norfolk, VA 23508 USA
[3] USN, Med Ctr Portsmouth, Portsmouth, VA USA
[4] Sobran, Fairfax, VA USA
[5] Univ S Florida, Coll Med, Tampa, FL USA
[6] Old Dominion Univ, Coll Hlth Sci, Norfolk, VA 23508 USA
基金:
美国国家卫生研究院;
关键词:
electroporation;
heart;
in vivo;
gene transfer;
swine;
ENDOTHELIAL GROWTH-FACTOR;
PLASMID DNA;
COLLATERAL DEVELOPMENT;
ISCHEMIC-MYOCARDIUM;
SKELETAL-MUSCLE;
BLOOD-FLOW;
THERAPY;
INJECTION;
DELIVERY;
D O I:
10.1038/gt.2012.15
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In vivo gene transfer to the ischemic heart via electroporation holds promise as a potential therapeutic approach for the treatment of heart disease. In the current study, we investigated the use of in vivo electroporation for gene transfer using three different penetrating electrodes and one non-penetrating electrode. The hearts of adult male swine were exposed through a sternotomy. Eight electric pulses synchronized to the rising phase of the R wave of the electrocardiogram were administered at varying pulse widths and field strengths following an injection of either a plasmid encoding luciferase or one encoding green fluorescent protein. Four sites on the anterior wall of the left ventricle were treated. Animals were killed 48 h after injection and electroporation and gene expression was determined. Results were compared with sites in the heart that received plasmid injection but no electric pulses or were not treated. Gene expression was higher in all electroporated sites when compared with injection only sites demonstrating the robustness of this approach. Our results provide evidence that in vivo electroporation can be a safe and effective non-viral method for delivering genes to the heart, in vivo. Gene Therapy (2013) 20, 151-157; doi:10.1038/gt.2012.15; published online 29 March 2012
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页码:151 / 157
页数:7
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