Rocher Christophe, Taanman Jan-Willem, Pierron Denis, Faustin Benjamin, Benard Giovani, Rossignol Rodrigue, Malgat Monique, Pedespan Laurence, Letellier Thierry
U688 INSERM-Université Victor Segalen Bordeaux2, 146 rue Léo-Saignat, 33076, Bordeaux-Cedex, France.
J Bioenerg Biomembr. 2008 Apr;40(2):59-67. doi: 10.1007/s10863-008-9130-5. Epub 2008 Apr 16.
The total amount of cellular mitochondrial DNA (mtDNA) varies widely and seems to be related to the nature and metabolic state of tissues and cells in culture. It is not known, however, whether this variation has any significance in vivo, and to which extent it regulates energy production. To better understand the importance of the cellular mtDNA level, we studied the influence of a gradual reduction of mtDNA copy number on oxidative phosphorylation in two models: (a) a control human cell line treated with different concentrations of 2', 3'-dideoxycytidine, a nucleoside analogue that inhibits mtDNA replication by interfering with mitochondrial DNA polymerase gamma, and (b) a cell line derived from a patient presenting mtDNA depletion. The two models were used to construct biochemical and phenotypic threshold curves. Our results show that oxidative phosphorylation activities are under a tight control by the amount of mtDNA in the cell, and that the full complement of mtDNA molecules are necessary to maintain a normal energy production level.
细胞线粒体DNA(mtDNA)的总量差异很大,似乎与培养中的组织和细胞的性质及代谢状态有关。然而,尚不清楚这种变异在体内是否具有任何意义,以及它在多大程度上调节能量产生。为了更好地理解细胞mtDNA水平的重要性,我们在两种模型中研究了mtDNA拷贝数逐渐减少对氧化磷酸化的影响:(a)用不同浓度的2',3'-二脱氧胞苷处理的对照人细胞系,2',3'-二脱氧胞苷是一种核苷类似物,通过干扰线粒体DNA聚合酶γ来抑制mtDNA复制;(b)源自一名线粒体DNA耗竭患者的细胞系。这两种模型用于构建生化和表型阈值曲线。我们的结果表明,氧化磷酸化活性受到细胞中mtDNA量的严格控制,并且mtDNA分子的完整互补对于维持正常的能量产生水平是必要的。