Quality control of mitochondria during aging: Is there a good and a bad side of mitochondrial dynamics?

被引:43
作者
Figge, Marc Thilo [1 ,2 ]
Osiewacz, Heinz D. [3 ]
Reichert, Andreas S. [4 ,5 ]
机构
[1] Hans Knoell Inst, HKI Ctr Syst Biol Infect, Leibniz Inst Nat Prod Res & Infect Biol, Jena, Germany
[2] Univ Jena, Jena, Germany
[3] Goethe Univ Frankfurt, Fac Biosci, D-60054 Frankfurt, Germany
[4] Goethe Univ Frankfurt, Buchmann Inst Mol Life Sci, D-60054 Frankfurt, Germany
[5] Goethe Univ Frankfurt, Zentrum Mol Med, D-60054 Frankfurt, Germany
关键词
aging; mitochondrial biology; mitochondrial dynamics; systems biology; LIFE-SPAN CONTROL; PODOSPORA-ANSERINA; OXIDATIVE STRESS; NEUROSPORA-INTERMEDIA; DNA REARRANGEMENTS; LIVING CELLS; FISSION; FUSION; MITOPHAGY; DEGRADATION;
D O I
10.1002/bies.201200125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Maintenance of functional mitochondria is essential in order to prevent degenerative processes leading to disease and aging. Mitochondrial dynamics plays a crucial role in ensuring mitochondrial quality but may also generate and spread molecular damage through a population of mitochondria. Computational simulations suggest that this dynamics is advantageous when mitochondria are not or only marginally damaged. In contrast, at a higher degree of damage, mitochondrial dynamics may be disadvantageous. Deceleration of fusion-fission cycles could be one way to adapt to this situation and to delay a further decline in mitochondrial quality. However, this adaptive response makes the mitochondrial network more vulnerable to additional molecular damage. The mitochondrial infectious damage adaptation (MIDA) model explains a number of inconsistent and counterintuitive data such as the clonal expansion of mutant mitochondrial DNA. We propose that mitochondrial dynamics is a double-edged sword and suggest ways to test this experimentally.
引用
收藏
页码:314 / 322
页数:9
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