The human mitochondrial KATP channel is modulated by calcium and nitric oxide:: a patch-clamp approach

被引:74
作者
Dahlem, YA
Horn, TFW
Buntinas, L
Gonoi, T
Wolf, G
Siemen, D
机构
[1] Univ Magdeburg, Inst Med Neurobiol, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Dept Neurol, D-39120 Magdeburg, Germany
[3] Chiba Univ, Res Ctr Pathogen Fungi & Microbial Toxicoses, Chiba 260, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2004年 / 1656卷 / 01期
关键词
apoptosis; oxidative stress; ischemic preconditioning; protection; diazoxide; 5-hydroxydecanoate;
D O I
10.1016/j.bbabio.2004.01.003
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
ATP-sensitive potassium channels of the inner mitochondrial membrane (mtK(ATp)) are blocked by ATP. They are suggested to be involved in protective mechanisms such as ischemic preconditioning (IPC). Here we identify this channel type for the first time in a human cell line (Jurkat cells). Vesicles of the inner mitochondrial membrane (mitoplasts) were prepared by hypoosmotic shock. Single-channel currents were measured by means of the patch-clamp technique. We identified an outward-rectifying channel with a slope conductance of 15 and 82 pS at negative and positive potentials, respectively. The block by 5-hydroxydecanoic acid and inhibition by ATP characterize this channel as the mtK(ATp) channel. ATP also increased the frequency of events within the burst. This effect was modulated by the Ca2+-bath concentration. We also show that the human mtK(ATp) channel is a direct target for nitric oxide that blocked the channel activity. Although the molecular structure of this channel type is still unknown, its characterization as an outward-rectifying channel and modulation by calcium ions and nitric oxide may help to elucidate its functional significance, which possibly implicates a role in cell survival after IPC. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 56
页数:11
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