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本文引用的文献

1
Ampk phosphorylation of Ulk1 is required for targeting of mitochondria to lysosomes in exercise-induced mitophagy.在运动诱导的线粒体自噬过程中,Ulk1的Ampk磷酸化是线粒体靶向溶酶体所必需的。
Nat Commun. 2017 Sep 15;8(1):548. doi: 10.1038/s41467-017-00520-9.
2
Fructose-1,6-bisphosphate and aldolase mediate glucose sensing by AMPK.果糖-1,6-二磷酸和醛缩酶通过AMPK介导葡萄糖感知。
Nature. 2017 Aug 3;548(7665):112-116. doi: 10.1038/nature23275. Epub 2017 Jul 19.
3
Systemic pan-AMPK activator MK-8722 improves glucose homeostasis but induces cardiac hypertrophy.系统泛 AMPK 激活剂 MK-8722 改善葡萄糖稳态,但诱导心脏肥大。
Science. 2017 Aug 4;357(6350):507-511. doi: 10.1126/science.aah5582. Epub 2017 Jul 13.
4
Acetyl-CoA synthetase regulates histone acetylation and hippocampal memory.乙酰辅酶A合成酶调节组蛋白乙酰化和海马体记忆。
Nature. 2017 Jun 15;546(7658):381-386. doi: 10.1038/nature22405. Epub 2017 May 31.
5
Nucleus-Translocated ACSS2 Promotes Gene Transcription for Lysosomal Biogenesis and Autophagy.细胞核易位的ACSS2促进溶酶体生物合成和自噬的基因转录。
Mol Cell. 2017 Jun 1;66(5):684-697.e9. doi: 10.1016/j.molcel.2017.04.026. Epub 2017 May 25.
6
Activation of Skeletal Muscle AMPK Promotes Glucose Disposal and Glucose Lowering in Non-human Primates and Mice.骨骼肌 AMPK 的激活促进非人类灵长类动物和小鼠的葡萄糖摄取和降低血糖。
Cell Metab. 2017 May 2;25(5):1147-1159.e10. doi: 10.1016/j.cmet.2017.04.010.
7
Liver-Specific Activation of AMPK Prevents Steatosis on a High-Fructose Diet.肝脏特异性激活AMPK可预防高果糖饮食引起的脂肪变性。
Cell Rep. 2017 Mar 28;18(13):3043-3051. doi: 10.1016/j.celrep.2017.03.011.
8
Canonical and noncanonical functions of ULK/Atg1.ULK/Atg1的典型和非典型功能。
Curr Opin Cell Biol. 2017 Apr;45:47-54. doi: 10.1016/j.ceb.2017.02.011. Epub 2017 Mar 11.
9
Autophagy maintains the metabolism and function of young and old stem cells.自噬维持年轻和衰老干细胞的新陈代谢及功能。
Nature. 2017 Mar 9;543(7644):205-210. doi: 10.1038/nature21388. Epub 2017 Mar 1.
10
AMPK signalling in health and disease.健康与疾病中的AMPK信号传导。
Curr Opin Cell Biol. 2017 Apr;45:31-37. doi: 10.1016/j.ceb.2017.01.005. Epub 2017 Feb 21.

AMPK:代谢和线粒体动态平衡的守护者。

AMPK: guardian of metabolism and mitochondrial homeostasis.

机构信息

The Salk Institute for Biological Studies, 10010 N. Torrey Pines Road, La Jolla, California 92037, USA.

出版信息

Nat Rev Mol Cell Biol. 2018 Feb;19(2):121-135. doi: 10.1038/nrm.2017.95. Epub 2017 Oct 4.

DOI:10.1038/nrm.2017.95
PMID:28974774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5780224/
Abstract

Cells constantly adapt their metabolism to meet their energy needs and respond to nutrient availability. Eukaryotes have evolved a very sophisticated system to sense low cellular ATP levels via the serine/threonine kinase AMP-activated protein kinase (AMPK) complex. Under conditions of low energy, AMPK phosphorylates specific enzymes and growth control nodes to increase ATP generation and decrease ATP consumption. In the past decade, the discovery of numerous new AMPK substrates has led to a more complete understanding of the minimal number of steps required to reprogramme cellular metabolism from anabolism to catabolism. This energy switch controls cell growth and several other cellular processes, including lipid and glucose metabolism and autophagy. Recent studies have revealed that one ancestral function of AMPK is to promote mitochondrial health, and multiple newly discovered targets of AMPK are involved in various aspects of mitochondrial homeostasis, including mitophagy. This Review discusses how AMPK functions as a central mediator of the cellular response to energetic stress and mitochondrial insults and coordinates multiple features of autophagy and mitochondrial biology.

摘要

细胞不断调整其代谢以满足其能量需求并响应营养物质的可用性。真核生物已经进化出一种非常复杂的系统,通过丝氨酸/苏氨酸激酶 AMP 激活蛋白激酶(AMPK)复合物来感知细胞内低 ATP 水平。在能量不足的情况下,AMPK 磷酸化特定的酶和生长控制节点,以增加 ATP 的生成并减少 ATP 的消耗。在过去的十年中,大量新的 AMPK 底物的发现使人们对重新编程细胞代谢从合成代谢到分解代谢所需的最少步骤有了更完整的理解。这种能量转换控制着细胞生长和其他几个细胞过程,包括脂质和葡萄糖代谢以及自噬。最近的研究表明,AMPK 的一个古老功能是促进线粒体健康,并且 AMPK 的多个新发现的靶标参与线粒体动态平衡的各个方面,包括线粒体自噬。这篇综述讨论了 AMPK 如何作为细胞对能量应激和线粒体损伤的反应的中央介质发挥作用,并协调自噬和线粒体生物学的多个特征。