Mitochondrial Aging and Age-Related Dysfunction of Mitochondria

被引:361
作者
Chistiakov, Dimitry A. [1 ]
Sobenin, Igor A. [2 ,3 ]
Revin, Victor V. [4 ]
Orekhov, Alexander N. [3 ,5 ]
Bobryshev, Yuri V. [4 ,6 ,7 ]
机构
[1] Pirogov Russian State Med Univ, Dept Med Nanobiotechnol, Moscow 117997, Russia
[2] Russian Cardiol Res & Prod Complex, Med Genet Lab, Moscow 121552, Russia
[3] Russian Acad Med Sci, Inst Gen Pathol & Pathophysiol, Lab Cellular Mech Atherogenesis, Moscow 125315, Russia
[4] NP Ogaryov Mordovian State Univ, Fac Biol, Saransk 430005, Russia
[5] Skolkovo Innovat Ctr, Atherosclerosis Res Inst, Moscow 143025, Russia
[6] Univ New S Wales, Fac Med, Sydney, NSW 2052, Australia
[7] Univ Western Sydney, Sch Med, Campbelltown, NSW 2560, Australia
关键词
SKELETAL-MUSCLE MITOCHONDRIAL; LIFE-SPAN; DNA MUTATIONS; OXIDATIVE CAPACITY; GENE-EXPRESSION; QUALITY-CONTROL; APOPTOSIS; EXERCISE; ATHEROSCLEROSIS; MECHANISMS;
D O I
10.1155/2014/238463
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Age-related changes in mitochondria are associated with decline in mitochondrial function. With advanced age, mitochondrial DNA volume, integrity and functionality decrease due to accumulation of mutations and oxidative damage induced by reactive oxygen species (ROS). In aged subjects, mitochondria are characterized by impaired function such as lowered oxidative capacity, reduced oxidative phosphorylation, decreased ATP production, significant increase in ROS generation, and diminished antioxidant defense. Mitochondrial biogenesis declines with age due to alterations in mitochondrial dynamics and inhibition of mitophagy, an autophagy process that removes dysfunctional mitochondria. Age-dependent abnormalities in mitochondrial quality control further weaken and impair mitochondrial function. In aged tissues, enhanced mitochondria-mediated apoptosis contributes to an increase in the percentage of apoptotic cells. However, implementation of strategies such as caloric restriction and regular physical training may delay mitochondrial aging and attenuate the age-related phenotype in humans.
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页数:7
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