Biological pacemakers based on If

被引:34
作者
Rosen, Michael R.
Brink, Peter R.
Cohen, Ira S.
Robinson, Richard B.
机构
[1] Univ Colorado, Coll Phys & Surg, Ctr Mol Therapeut, Dept Pharmacol, New York, NY 10032 USA
[2] Columbia Univ, Dept Pediat, New York, NY USA
[3] SUNY Stony Brook, Inst Mol Cardiol, Dept Physiol, Stony Brook, NY USA
[4] SUNY Stony Brook, Inst Mol Cardiol, Dept Biophys, Stony Brook, NY USA
关键词
HCN isoforms; electronic pacemakers; sinoatrial node; atrioventricular block; gene therapy; cell therapy;
D O I
10.1007/s11517-006-0060-2
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Biological pacemaking as a replacement for or adjunct to electronic pacemakers has been a subject of interest since the 1990s. In the following pages, we discuss the rational for and progress made using a hyperpolarization activated, cyclic nucleotide gated channel isoform to carry the I (f) pacemaker current in gene and cell therapy approaches. Both strategies have resulted in effective biological pacemaker function over a period of weeks in intact animals. Moreover, the use of adult human mesenchymal stem cells as a platform for carrying pacemaker genes has resulted in the formation of functional gap junctions with cardiac myocytes in situ leading to effective and persistent propagation of pacemaker current. The approaches described are encouraging, suggesting that biological pacemakers based on this strategy can be brought to clinical testing.
引用
收藏
页码:157 / 166
页数:10
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