Karavaeva I E, Shekhireva K V, Severin F F, Knorre D A
Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, 119992, Russia.
Biochemistry (Mosc). 2015 May;80(5):549-58. doi: 10.1134/S0006297915050053.
Dissipation of transmembrane potential inhibits mitochondrial fusion and thus prevents reintegration of damaged mitochondria into the mitochondrial network. Consequently, damaged mitochondria are removed by autophagy. Does transmembrane potential directly regulate the mitochondrial fusion machinery? It was shown that inhibition of ATP-synthase induces fragmentation of mitochondria while preserving transmembrane potential. Moreover, mitochondria of the yeast Saccharomyces cerevisiae retain the ability to fuse even in the absence of transmembrane potential. Metazoan mitochondria in some cases retain ability to fuse for a short period even in a depolarized state. It also seems unlikely that transmembrane potential-based regulation of mitochondrial fusion would prevent reintegration of mitochondria with damaged ATP-synthase into the mitochondrial network. Such reintegration could lead to clonal expansion of mtDNAs harboring deleterious mutations in ATP synthase. We speculate that transmembrane potential is not directly involved in regulation of mitochondrial fusion but affects mitochondrial NTP/NDP ratio, which in turn regulates their fusion.
跨膜电位的消散会抑制线粒体融合,从而阻止受损线粒体重新整合到线粒体网络中。因此,受损线粒体通过自噬被清除。跨膜电位是否直接调节线粒体融合机制?研究表明,抑制ATP合酶会导致线粒体碎片化,同时保留跨膜电位。此外,酿酒酵母的线粒体即使在没有跨膜电位的情况下也保留融合能力。在某些情况下,后生动物的线粒体即使在去极化状态下也能在短时间内保留融合能力。基于跨膜电位对线粒体融合的调节似乎也不太可能阻止带有受损ATP合酶的线粒体重新整合到线粒体网络中。这种重新整合可能导致ATP合酶中携带有害突变的线粒体DNA的克隆扩增。我们推测跨膜电位不直接参与线粒体融合的调节,而是影响线粒体的NTP/NDP比率,进而调节它们的融合。