自噬
NAD+激酶
生物
细胞生物学
长寿
细胞内
线粒体
新陈代谢
代谢物
酶
生物化学
遗传学
细胞凋亡
作者
Niall Wilson,Tetsushi Kataura,Miriam E. Korsgen,Congxin Sun,Sovan Sarkar,Viktor I. Korolchuk
标识
DOI:10.1016/j.tcb.2023.02.004
摘要
Autophagy is an intracellular degradation pathway that recycles subcellular components to maintain metabolic homeostasis. NAD is an essential metabolite that participates in energy metabolism and serves as a substrate for a series of NAD+-consuming enzymes (NADases), including PARPs and SIRTs. Declining levels of autophagic activity and NAD represent features of cellular ageing, and consequently enhancing either significantly extends health/lifespan in animals and normalises metabolic activity in cells. Mechanistically, it has been shown that NADases can directly regulate autophagy and mitochondrial quality control. Conversely, autophagy has been shown to preserve NAD levels by modulating cellular stress. In this review we highlight the mechanisms underlying this bidirectional relationship between NAD and autophagy, and the potential therapeutic targets it provides for combatting age-related disease and promoting longevity.
科研通智能强力驱动
Strongly Powered by AbleSci AI