丙酮酸脱氢酶复合物
柠檬酸循环
可药性
生物
氧化磷酸化
糖酵解
生物能学
代谢途径
生物化学
线粒体
细胞生物学
新陈代谢
酶
基因
作者
Peter W. Stacpoole,Charles E. McCall
出处
期刊:Mitochondrion
[Elsevier]
日期:2023-05-01
卷期号:70: 59-102
被引量:18
标识
DOI:10.1016/j.mito.2023.02.007
摘要
Found in all organisms, pyruvate dehydrogenase complexes (PDC) are the keystones of prokaryotic and eukaryotic energy metabolism. In eukaryotic organisms these multi-component megacomplexes provide a crucial mechanistic link between cytoplasmic glycolysis and the mitochondrial tricarboxylic acid (TCA) cycle. As a consequence, PDCs also influence the metabolism of branched chain amino acids, lipids and, ultimately, oxidative phosphorylation (OXPHOS). PDC activity is an essential determinant of the metabolic and bioenergetic flexibility of metazoan organisms in adapting to changes in development, nutrient availability and various stresses that challenge maintenance of homeostasis. This canonical role of the PDC has been extensively probed over the past decades by multidisciplinary investigations into its causal association with diverse physiological and pathological conditions, the latter making the PDC an increasingly viable therapeutic target. Here we review the biology of the remarkable PDC and its emerging importance in the pathobiology and treatment of diverse congenital and acquired disorders of metabolic integration.
科研通智能强力驱动
Strongly Powered by AbleSci AI