线粒体
氧化磷酸化
生物
新陈代谢
调节器
生物化学
功能(生物学)
代谢途径
硫辛酸
脂肪酸代谢
β氧化
氧化代谢
脂肪酸
细胞生物学
基因
抗氧化剂
作者
Riley Wedan,Jacob Z. Longenecker,Sara M. Nowinski
标识
DOI:10.1016/j.cmet.2023.11.017
摘要
Summary
Contrary to their well-known functions in nutrient breakdown, mitochondria are also important biosynthetic hubs and express an evolutionarily conserved mitochondrial fatty acid synthesis (mtFAS) pathway. mtFAS builds lipoic acid and longer saturated fatty acids, but its exact products, their ultimate destination in cells, and the cellular significance of the pathway are all active research questions. Moreover, why mitochondria need mtFAS despite their well-defined ability to import fatty acids is still unclear. The identification of patients with inborn errors of metabolism in mtFAS genes has sparked fresh research interest in the pathway. New mammalian models have provided insights into how mtFAS coordinates many aspects of oxidative mitochondrial metabolism and raise questions about its role in diseases such as obesity, diabetes, and heart failure. In this review, we discuss the products of mtFAS, their function, and the consequences of mtFAS impairment across models and in metabolic disease.
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