Molecular composition of mitochondrial ATP-sensitive potassium channels probed by viral Kir gene transfer

被引:76
作者
Seharaseyon, J
Ohler, A
Sasaki, N
Fraser, H
Sato, T
Johns, DC
O'Rourke, B
Marbán, E
机构
[1] Johns Hopkins Univ, Dept Med, Inst Mol Cardiobiol, Baltimore, MD 21205 USA
[2] Oita Med Univ, Dept Physiol, Oita 8795593, Japan
关键词
mitochondrial mitoK(ATP) channel (mitoK(ATP)) potassium inward rectifier (Kir); adenoviral gene transfer; flavoprotein fluorescence;
D O I
10.1006/jmcc.2000.1226
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heart cells contain ATP-sensitive potassium (K-APT) channels in both the sarcolemma and the inner mitochondrial membrane. The sarcolemmal channels are believed to be heteromultimeric complexes of sulfonylurea receptors (SUR) and potassium inward rectifier (Kir) gene products, but the molecular identity of mitochondrial K-ATP (mitoK(ATP)) channels remains unclear. To probe the molecular composition of It, channels, we used adenoviral gene transfer to express wild-type (WT) and dominant-negative (AFA) constructs of Kir6.1 and 6.2 in rabbit ventricular myocytes. None of the Kir6.1 or 6.2 constructs affected mitoK(ATP) channel activity as assayed by confocal imaging of flavoprotein fluorescence, contradicting the proposal, based on subcellular antibody localization, that Kir6.1 forms part of mitoK(ATP) channels. As previously reported, dominant-negative Kir6.2 gene transfer suppressed sarcolemmal K-ATP current, while Kir6.1 constructs had no effect on sarcolemmal activity. Immunohistochemistry with an anti-Kir6.1 antibody revealed expression of this protein in heart but no apparent co-localization with mitochondria. Thus, the available evidence indicates that both Kir6.1 and 6.2 are expressed in ventricular myocytes, but neither plays a discernible functional role in the mitoK(ATP) channel. (C) 2000 Academic Press.
引用
收藏
页码:1923 / 1930
页数:8
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