Crompton M, Andreeva L
Department of Biochemistry and Molecular Biology, University College London, U.K.
Biochem J. 1994 Aug 15;302 ( Pt 1)(Pt 1):181-5. doi: 10.1042/bj3020181.
The mitochondrial inner membrane contains a Ca(2+)-activated pore of possible relevance to the pathogenesis of ischaemia/reperfusion injury which is inhibited by the immunosuppressant cyclosporin A (CSA). The present study employs a number of novel cobaltammine complex inhibitors of the Ca2+ uniporter (mediating Ca2+ uptake) to examine whether intramitochondrial Ca2+ influences the capacity of CSA to block the pore. Using dissipation of the inner membrane potential as a means of monitoring the state of the pore, it is shown that CSA blockade is facilitated as Ca2+ uptake is restricted. Ca2+ also depresses and reverses the binding of [3H]CSA to mitochondria, but Ca2+ is ineffective when its uptake is prevented. It is concluded that a high intramitochondrial Ca2+ concentration antagonizes pore inhibition by CSA. The significance of this is discussed.
线粒体内膜含有一种可能与缺血/再灌注损伤发病机制相关的Ca(2+)激活孔道,免疫抑制剂环孢素A(CSA)可抑制该孔道。本研究采用了多种新型的钙离子单向转运体(介导钙离子摄取)钴氨络合物抑制剂,以研究线粒体内钙离子是否影响CSA阻断该孔道的能力。以内膜电位的消散作为监测孔道状态的手段,结果表明,随着钙离子摄取受限,CSA的阻断作用得到促进。钙离子还会降低并逆转[3H]CSA与线粒体的结合,但当钙离子摄取被阻止时则无效。得出的结论是,高线粒体内钙离子浓度会拮抗CSA对孔道的抑制作用。并讨论了其意义。