Control of mitochondrial integrity in ageing and disease

被引:50
作者
Szklarczyk, Radek [1 ,3 ]
Nooteboom, Marco [2 ]
Osiewacz, Heinz D. [4 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Ctr Mol & Biomol Informat, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Mol Life Sci, Dept Biochem 286, NL-6500 HB Nijmegen, Netherlands
[3] Maastricht Univ, Med Ctr, Unit Clin Genom, Dept Clin Genet, NL-6200 MD Maastricht, Netherlands
[4] Goethe Univ Frankfurt, Fac Biosci & Cluster Excellence Macromol Complexe, D-60438 Frankfurt, Germany
关键词
mitochondria; quality control; disease; ageing; M-AAA PROTEASE; DNA-POLYMERASE-GAMMA; DYNAMIN-RELATED PROTEIN; DOMINANT OPTIC ATROPHY; BASE EXCISION-REPAIR; PLASMID-LIKE DNA; SPASTIC PARAPLEGIA; METHIONINE SULFOXIDE; POINT MUTATIONS; QUALITY-CONTROL;
D O I
10.1098/rstb.2013.0439
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Various molecular and cellular pathways are active in eukaryotes to control the quality and integrity of mitochondria. These pathways are involved in keeping a 'healthy' population of this essential organelle during the lifetime of the organism. Quality control (QC) systems counteract processes that lead to organellar dysfunction manifesting as degenerative diseases and ageing. We discuss disease-and ageing-related pathways involved in mitochondrial QC: mtDNA repair and reorganization, regeneration of oxidized amino acids, refolding and degradation of severely damaged proteins, degradation of whole mitochondria by mitophagy and finally programmed cell death. The control of the integrity of mtDNA and regulation of its expression is essential to remodel single proteins as well as mitochondrial complexes that determine mitochondrial functions. The redundancy of components, such as proteases, and the hierarchies of the QC raise questions about crosstalk between systems and their precise regulation. The understanding of the underlying mechanisms on the genomic, proteomic, organellar and cellular levels holds the key for the development of interventions for mitochondrial dysfunctions, degenerative processes, ageing and age-related diseases resulting from impairments of mitochondria.
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页数:18
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