Mitochondrial anomalies: driver to age associated degenerative human ailments

被引:19
作者
Bunkar, Neha [1 ]
Bhargava, Arpit [1 ,2 ]
Khare, Naveen Kumar [2 ]
Mishra, Pradyumna Kumar [1 ,2 ]
机构
[1] Dr HS Gour Cent Univ, Sch Biol Sci, Sagar, India
[2] ACTREC, Tata Mem Ctr, Div Translat Res, Bombay, Maharashtra, India
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2016年 / 21卷
关键词
Mitochondrial Dysfunction; Oxidative Stress; Oxidative Damage; Redox Signaling; Review; Mitochondria Targeting; AMYOTROPHIC-LATERAL-SCLEROSIS; LIPOSOME-BASED CARRIER; NUCLEAR CROSS-TALK; OXIDATIVE STRESS; MITO-PORTER; SKELETAL-MUSCLE; CELL-DEATH; TARGETED NANOPARTICLES; EXPRESSION CHANGES; DENDRITIC CELLS;
D O I
10.2741/4420
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 play a fundamental role in regulating a variety of complex metabolic processes to maintain adequate energy balance for cellular existence. To orchestrate these functions, an undisturbed mitochondrial dynamics is imperative through a set of tightly guided mechanisms. Interference in key signature processes by several genetic, epigenetic and age-linked factors triggers mitochondrial dysfunction through decrease in mitochondrial biogenesis, reduced mitochondrial content, aberrant mtDNA mutations, increased oxidative stress, deficient mitophagy, energy dysfunction, decrease in anti oxidant defense and impaired calcium homeostasis. Mitochondrial dysfunction is widely implicated in origin and development of various age associated degenerative human ailments including metabolic syndromes, cardiovascular diseases, cancer, diabetes and neurodegenerative disorders. The present review revisits the mitochondrial anomalies involved in aetiology of different human diseases and also highlights the translational significance of nano-vectors aimed for selective mitochondrial engineering which might pave way for development of novel therapeutics.
引用
收藏
页码:769 / 793
页数:25
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