线粒体
过氧化物酶体
脂质代谢
内质网
细胞生物学
活性氧
生物
三磷酸腺苷
平衡
生物化学
新陈代谢
氧化磷酸化
生物能学
化学
基因
作者
Siresha Bathina,Undurti N. Das
出处
期刊:Discovery Medicine
日期:2023-01-01
卷期号:35 (178): 653-653
标识
DOI:10.24976/discov.med.202335178.64
摘要
Mitochondria-associated membranes (MAMs) play a significant role in multiple cellular processes including lipid metabolism and neuronal survival. Fatty acids constitute 80% of the dry mass of the brain and are vital for life. Apart from mitochondrial β-oxidation, fatty acids are metabolized in part by peroxisomes to regulate the generation of acyl Coenzyme A and adenosine triphosphate (ATP). Ablation of mitochondria and its associated genes tether endoplasmic reticulum (ER)-Mitochondria contact and results in loss of function leading to aberrant lipid metabolism. Additionally, an increase in reactive oxygen species (ROS) levels along with free radicals' generation may lead to alteration in the integrity of membrane phospholipids, proteins, and DNA. Hence, it is critical to understand the effect of structural and functional aspects of mitochondria on lipid homeostasis. This review explains the role of mitochondrial dysfunction in lipid metabolism and its impact on various neurodegenerative diseases and metabolic disorders.
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