Su Tianhong, Turnbull Doug M, Greaves Laura C
Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
LLHW Centre for Aging and Vitality, Newcastle University Institute for Aging, The Medical School, Newcastle upon Tyne NE2 4HH, UK.
Genes (Basel). 2018 Mar 27;9(4):182. doi: 10.3390/genes9040182.
Mitochondrial DNA (mtDNA) mutations accumulate in somatic stem cells during ageing and cause mitochondrial dysfunction. In this review, we summarize the studies that link mtDNA mutations to stem cell ageing. We discuss the age-related behaviours of the somatic mtDNA mutations in stem cell populations and how they potentially contribute to stem cell ageing by altering mitochondrial properties in humans and in mtDNA-mutator mice. We also draw attention to the diverse fates of the mtDNA mutations with different origins during ageing, with potential selective pressures on the germline inherited but not the somatic mtDNA mutations.
线粒体DNA(mtDNA)突变在衰老过程中会在体干细胞中积累,并导致线粒体功能障碍。在本综述中,我们总结了将mtDNA突变与干细胞衰老联系起来的研究。我们讨论了体干细胞群体中线粒体DNA突变与年龄相关的行为,以及它们如何通过改变人类和线粒体DNA突变小鼠的线粒体特性,潜在地导致干细胞衰老。我们还提请注意衰老过程中不同起源的线粒体DNA突变的不同命运,以及对种系遗传而非体细胞线粒体DNA突变的潜在选择压力。