线粒体DNA
线粒体
生物
粒线体疾病
氧化应激
分子医学
计算生物学
DNAJA3公司
线粒体融合
细胞生物学
遗传学
生物信息学
细胞
基因
生物化学
细胞周期
作者
Yiyuan Yin,Haitao Shen
标识
DOI:10.3892/ijmm.2022.5182
摘要
Mitochondrial abnormalities are primarily seen in morphology, structure and function. They can cause damage to organs, including the heart, brain and muscle, by various mechanisms, such as oxidative stress, abnormal energy metabolism, or genetic mutations. Identifying and detecting pathophysiological alterations in mitochondria is the principal means of studying mitochondrial abnormalities. The present study reviewed methods in mitochondrial research and focused on three aspects: Mitochondrial extraction and purification, morphology and structure and function. In addition to classical methods, such as electron microscopy and mitochondrial membrane potential monitoring, newly developed methods, such as mitochondrial ultrastructural determination, mtDNA mutation assays, metabolomics and analyses of regulatory mechanisms, have also been utilized in recent years. These approaches enable the accurate detection of mitochondrial abnormalities and provide guidance for the diagnosis and treatment of related diseases.
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