The Ageing Brain: Molecular and Cellular Basis of Neurodegeneration

被引:122
|
作者
Azam, Shofiul [1 ]
Haque, Md Ezazul [1 ]
Balakrishnan, Rengasamy [1 ]
Kim, In-Su [2 ]
Choi, Dong-Kug [1 ,2 ]
机构
[1] Konkuk Univ, Grad Sch, Dept Appl Life Sci, BK21 Program, Chungju Si, South Korea
[2] Konkuk Univ, Coll Biomed & Hlth Sci, Res Inst Inflammatory Dis RID, Dept Biotechnol, Chungju Si, South Korea
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 09卷
基金
新加坡国家研究基金会;
关键词
neurodegenerative diseases; NAD(+); aggregation; mitophagy; inflammation; AMYOTROPHIC-LATERAL-SCLEROSIS; ALZHEIMERS-DISEASE; MITOCHONDRIAL DYSFUNCTION; HUNTINGTONS-DISEASE; AMYLOID-BETA; DNA-DAMAGE; PARKINSONS-DISEASE; OXIDATIVE STRESS; POLY(ADP-RIBOSE) POLYMERASES; COGNITIVE IMPAIRMENT;
D O I
10.3389/fcell.2021.683459
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ageing is an inevitable event in the lifecycle of all organisms, characterized by progressive physiological deterioration and increased vulnerability to death. Ageing has also been described as the primary risk factor of most neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), and frontotemporal lobar dementia (FTD). These neurodegenerative diseases occur more prevalently in the aged populations. Few effective treatments have been identified to treat these epidemic neurological crises. Neurodegenerative diseases are associated with enormous socioeconomic and personal costs. Here, the pathogenesis of AD, PD, and other neurodegenerative diseases has been presented, including a summary of their known associations with the biological hallmarks of ageing: genomic instability, telomere attrition, epigenetic alterations, loss of proteostasis, mitochondrial dysfunction, cellular senescence, deregulated nutrient sensing, stem cell exhaustion, and altered intercellular communications. Understanding the central biological mechanisms that underlie ageing is important for identifying novel therapeutic targets for neurodegenerative diseases. Potential therapeutic strategies, including the use of NAD(+) precursors, mitophagy inducers, and inhibitors of cellular senescence, has also been discussed.
引用
收藏
页数:22
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