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健康与疾病状态下体内能量通量反馈调节中的结构-功能关系:线粒体相互作用体

Structure-function relationships in feedback regulation of energy fluxes in vivo in health and disease: mitochondrial interactosome.

作者信息

Saks Valdur, Guzun Rita, Timohhina Natalja, Tepp Kersti, Varikmaa Minna, Monge Claire, Beraud Nathalie, Kaambre Tuuli, Kuznetsov Andrey, Kadaja Lumme, Eimre Margus, Seppet Enn

机构信息

Laboratory of Fundamental and Applied Bioenergetics, INSERM U884, Joseph Fourier University, Grenoble, France.

出版信息

Biochim Biophys Acta. 2010 Jun-Jul;1797(6-7):678-97. doi: 10.1016/j.bbabio.2010.01.011. Epub 2010 Jan 21.

Abstract

The aim of this review is to analyze the results of experimental research of mechanisms of regulation of mitochondrial respiration in cardiac and skeletal muscle cells in vivo obtained by using the permeabilized cell technique. Such an analysis in the framework of Molecular Systems Bioenergetics shows that the mechanisms of regulation of energy fluxes depend on the structural organization of the cells and interaction of mitochondria with cytoskeletal elements. Two types of cells of cardiac phenotype with very different structures were analyzed: adult cardiomyocytes and continuously dividing cancerous HL-1 cells. In cardiomyocytes mitochondria are arranged very regularly, and show rapid configuration changes of inner membrane but no fusion or fission, diffusion of ADP and ATP is restricted mostly at the level of mitochondrial outer membrane due to an interaction of heterodimeric tubulin with voltage dependent anion channel, VDAC. VDAC with associated tubulin forms a supercomplex, Mitochondrial Interactosome, with mitochondrial creatine kinase, MtCK, which is structurally and functionally coupled to ATP synthasome. Due to selectively limited permeability of VDAC for adenine nucleotides, mitochondrial respiration rate depends almost linearly upon the changes of cytoplasmic ADP concentration in their physiological range. Functional coupling of MtCK with ATP synthasome amplifies this signal by recycling adenine nucleotides in mitochondria coupled to effective phosphocreatine synthesis. In cancerous HL-1 cells this complex is significantly modified: tubulin is replaced by hexokinase and MtCK is lacking, resulting in direct utilization of mitochondrial ATP for glycolytic lactate production and in this way contributing in the mechanism of the Warburg effect. Systemic analysis of changes in the integrated system of energy metabolism is also helpful for better understanding of pathogenesis of many other diseases.

摘要

本综述的目的是分析运用透化细胞技术在体内获得的关于心肌和骨骼肌细胞线粒体呼吸调节机制的实验研究结果。在分子系统生物能学框架下进行的此类分析表明,能量通量的调节机制取决于细胞的结构组织以及线粒体与细胞骨架成分的相互作用。分析了两种结构差异极大的具有心脏表型的细胞:成年心肌细胞和持续分裂的癌性HL-1细胞。在心肌细胞中,线粒体排列非常规则,内膜呈现快速的构象变化,但无融合或裂变现象,由于异二聚体微管蛋白与电压依赖性阴离子通道(VDAC)相互作用,ADP和ATP的扩散主要在线粒体外膜水平受到限制。与微管蛋白相关的VDAC与线粒体肌酸激酶(MtCK)形成一个超复合物,即线粒体相互作用体,它在结构和功能上与ATP合酶体相耦合。由于VDAC对腺嘌呤核苷酸的选择性有限通透性,线粒体呼吸速率在其生理范围内几乎线性地依赖于细胞质ADP浓度的变化。MtCK与ATP合酶体的功能耦合通过在线粒体中循环利用腺嘌呤核苷酸并与有效的磷酸肌酸合成相耦合来放大这一信号。在癌性HL-1细胞中,这种复合物发生了显著改变:微管蛋白被己糖激酶取代且缺乏MtCK,导致线粒体ATP直接用于糖酵解产生乳酸,从而促成了瓦伯格效应机制。对能量代谢整合系统变化的系统分析也有助于更好地理解许多其他疾病的发病机制。

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