Proteomic profiling of mitochondria: what does it tell us about the ageing brain?

被引:20
|
作者
Ingram, Thomas [1 ]
Chakrabarti, Lisa [1 ]
机构
[1] Univ Nottingham, Fac Med, SVMS, Loughborough LE12 5RD, England
来源
AGING-US | 2016年 / 8卷 / 12期
基金
英国生物技术与生命科学研究理事会;
关键词
mitochondria; aging; proteomics; HEAT-SHOCK PROTEINS; ALPHA-SYNUCLEIN AGGREGATION; DYNAMIN-RELATED PROTEIN-1; DEPENDENT ANION CHANNELS; LONGEST-LIVING RODENT; RAT SKELETAL-MUSCLE; CITRIC-ACID CYCLE; NAKED MOLE-RAT; NF-KAPPA-B; PARKINSONS-DISEASE;
D O I
10.18632/aging.101131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial dysfunction is evident in numerous neurodegenerative and age-related disorders. It has also been linked to cellular ageing, however our current understanding of the mitochondrial changes that occur are unclear. Functional studies have made some progress reporting reduced respiration, dynamic structural modifications and loss of membrane potential, though there are conflicts within these findings. Proteomic analyses, together with functional studies, are required in order to profile the mitochondrial changes that occur with age and can contribute to unravelling the complexity of the ageing phenotype. The emergence of improved protein separation techniques, combined with mass spectrometry analyses has allowed the identification of age and cell-type specific mitochondrial changes in energy metabolism, antioxidants, fusion and fission machinery, chaperones, membrane proteins and biosynthesis pathways. Here, we identify and review recent data from the analyses of mitochondria from rodent brains. It is expected that knowledge gained from understanding age-related mitochondrial changes of the brain should lead to improved biomarkers of normal ageing and also age-related disease progression.
引用
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页码:3161 / 3179
页数:19
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