Mitochondrial quality control: Epigenetic signatures and therapeutic strategies

被引:18
|
作者
Ambekar, Tanuja [1 ]
Pawar, Jyoti [1 ]
Rathod, Ramdev [1 ]
Patel, Monica [1 ]
Fernandes, Valencia [1 ]
Kumar, Rahul [1 ]
Singh, Shashi Bala [1 ]
Khatri, Dharmendra Kumar [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmacol & Toxicol, Hyderabad 500037, Telangana, India
关键词
Neurodegeneration; Biogenesis; Mitophagy; Mitochondrial quality control; DNA methylation; Histone acetylation; COMPLEX-I; PARKINSONS-DISEASE; BIOGENESIS CONTRIBUTES; SUPEROXIDE-DISMUTASE; HUNTINGTONS-DISEASE; DNA METHYLATION; CELLULAR-MODEL; URSOLIC ACID; DYSFUNCTION; ACTIVATION;
D O I
10.1016/j.neuint.2021.105095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are semi-autonomous organelle staging a crucial role in cellular stress response, energy metabolism and cell survival. Maintaining mitochondrial quality control is very important for its homeostasis. Pathological conditions such as oxidative stress and neurodegeneration, disrupt this quality control, and involvement of genetic and epigenetic materials in this disruption have been reported. These regulatory factors trigger mitochondrial imbalance, as seen in many neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, Amyotrophic lateral sclerosis, and Huntington's disease. The dynamic regulatory pathways i.e. mitophagy, biogenesis, permeability pore transitioning, fusion-fission are affected as a consequence and have been reviewed in this article. Moreover, several epigenetic mechanisms such as DNA methylation and histone modulation participating in such neurological disorders have also been discussed. Apart from it, therapeutic approaches targeting mitochondrial quality control have been tremendously explored showing ameliorative effects for these diseases, and have been discussed here with a novel perspective.
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页数:10
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