Silencing the cardiac potassium channel Kv4.3 by RNA interference in a CHO expression system
被引:10
作者:
Cotella, D
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机构:Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Cotella, D
Jost, N
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机构:Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Jost, N
Darna, M
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机构:Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Darna, M
Radicke, S
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机构:Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Radicke, S
Ravens, U
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机构:Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Ravens, U
Wettwer, E
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机构:
Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, GermanyTech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
Wettwer, E
[1
]
机构:
[1] Tech Univ, Carl Gustav Carus Med Fac, Dept Pharmacol & Toxicol, Dresden, Germany
[2] Med Univ, Dept Pharmacol & Pharmacotherapy, Szeged, Hungary
(It)o;
Kv4.3;
ion channels;
RNA interference;
siRNA;
gene silencing;
CHO cell;
D O I:
10.1016/j.bbrc.2005.03.018
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
RNA interference (RNAi) is a powerful technique for gene silencing, in which the downregulation of mRNA is triggered by short RNAs complementary to a target mRNA sequence, with consequent reduction of the encoded protein. The aim of this study was to test the effects of silencing the expression of the cardiac potassium channel Kv4.3 in a heterologous expression system, in order to investigate the effect of RNAi on channel properties. A Chinese hamster ovary cell line stably expressing Kv4.3 and the accessory P-subunit KChIP2 was transfected with small-interfering RNAs (siRNAs) targeting Kv4.3. Effects of RNAi were monitored at the mRNA, protein, and functional levels. Real-time PCR and immunofluorescence staining revealed significant reduction of Kv4.3 mRNA and protein expression. These results were confirmed by functional patch-clamp measurements of the transient outward current (I-to) which was reduced up to 80% by RNAi. We conclude that the use of siRNAs reagents for post-transcriptional gene silencing is a new effective method for the reduction of the expression and function of different ionic channels which may be adapted for studying their role also in native cells. (c) 2005 Elsevier Inc. All rights reserved.
机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Himmel, HM
;
Pietsch, M
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机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Pietsch, M
;
Streller, U
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机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Streller, U
;
Graf, EM
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机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Graf, EM
;
Ravens, U
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机构:
Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, GermanyTech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Himmel, HM
;
Pietsch, M
论文数: 0引用数: 0
h-index: 0
机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Pietsch, M
;
Streller, U
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h-index: 0
机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Streller, U
;
Graf, EM
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h-index: 0
机构:Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany
Graf, EM
;
Ravens, U
论文数: 0引用数: 0
h-index: 0
机构:
Tech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, GermanyTech Univ Dresden, Inst Pharmakol & Toxikol, Med Fak Carl Gustav Carus, D-01307 Dresden, Germany