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Interdependence of AMPK and SIRT1 for metabolic adaptation to fasting and exercise in skeletal muscle.AMPK 和 SIRT1 在骨骼肌适应禁食和运动中的代谢中的相互依赖关系。
Cell Metab. 2010 Mar 3;11(3):213-9. doi: 10.1016/j.cmet.2010.02.006.
2
SRT1720, SRT2183, SRT1460, and resveratrol are not direct activators of SIRT1.SRT1720、SRT2183、SRT1460 和白藜芦醇不是 SIRT1 的直接激活剂。
J Biol Chem. 2010 Mar 12;285(11):8340-51. doi: 10.1074/jbc.M109.088682. Epub 2010 Jan 8.
3
JNK1 phosphorylates SIRT1 and promotes its enzymatic activity.JNK1 磷酸化 SIRT1 并促进其酶活性。
PLoS One. 2009 Dec 22;4(12):e8414. doi: 10.1371/journal.pone.0008414.
4
PKA phosphorylates and inactivates AMPKalpha to promote efficient lipolysis.蛋白激酶 A(PKA)使 AMPKα 磷酸化而失活,从而促进脂肪的有效分解。
EMBO J. 2010 Jan 20;29(2):469-81. doi: 10.1038/emboj.2009.339. Epub 2009 Nov 26.
5
AMP-activated protein kinase-deficient mice are resistant to the metabolic effects of resveratrol.AMP 激活的蛋白激酶缺陷型小鼠对白藜芦醇的代谢作用具有抗性。
Diabetes. 2010 Mar;59(3):554-63. doi: 10.2337/db09-0482. Epub 2009 Nov 23.
6
AMP-activated protein kinase adapts rRNA synthesis to cellular energy supply.AMP激活的蛋白激酶使核糖体RNA合成适应细胞能量供应。
Proc Natl Acad Sci U S A. 2009 Oct 20;106(42):17781-6. doi: 10.1073/pnas.0909873106. Epub 2009 Oct 6.
7
Oxaloacetate supplementation increases lifespan in Caenorhabditis elegans through an AMPK/FOXO-dependent pathway.草酰乙酸盐补充通过 AMPK/FOXO 依赖途径增加秀丽隐杆线虫的寿命。
Aging Cell. 2009 Dec;8(6):765-8. doi: 10.1111/j.1474-9726.2009.00527.x. Epub 2009 Sep 30.
8
The role of sirtuins in the control of metabolic homeostasis.沉默调节蛋白在代谢稳态调控中的作用。
Ann N Y Acad Sci. 2009 Sep;1173 Suppl 1(0 1):E10-9. doi: 10.1111/j.1749-6632.2009.04952.x.
9
FoxO1 and HNF-4 are involved in regulation of hepatic glucokinase gene expression by resveratrol.叉头框蛋白O1(FoxO1)和肝细胞核因子4(HNF-4)参与白藜芦醇对肝脏葡萄糖激酶基因表达的调控。
J Biol Chem. 2009 Nov 6;284(45):30783-97. doi: 10.1074/jbc.M109.045260. Epub 2009 Sep 9.
10
Caloric restriction, SIRT1 and longevity.热量限制、SIRT1与长寿
Trends Endocrinol Metab. 2009 Sep;20(7):325-31. doi: 10.1016/j.tem.2009.03.008. Epub 2009 Aug 25.

AMP 激活的蛋白激酶及其下游转录途径。

AMP-activated protein kinase and its downstream transcriptional pathways.

机构信息

Laboratory of Integrative and Systems Physiology, Ecole Polytechnique Fédérale de Lausanne (EPFL), SV-IBI, Building AI, Station 15, Lausanne, Switzerland.

出版信息

Cell Mol Life Sci. 2010 Oct;67(20):3407-23. doi: 10.1007/s00018-010-0454-z. Epub 2010 Jul 17.

DOI:10.1007/s00018-010-0454-z
PMID:20640476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3622821/
Abstract

The AMP-activated protein kinase (AMPK) is a key regulator of catabolic versus anabolic processes. Its properties as an energy sensor allow it to couple the energy status of the cell to the metabolic environment. These adaptations not only take place through the acute modulation of key metabolic enzymes via direct phosphorylation, but also through a slower transcriptional adaptative response. The question of how AMPK regulates the expression of a number of gene sets, such as those related to mitochondrial biogenesis, energy production and oxidative protection, is only beginning to be elucidated, and still many questions remain to be answered. In this review we will try to integrate our current knowledge on how AMPK regulates transcription in muscle and liver, which will serve as examples to illustrate the major advances in the field and the key challenges ahead.

摘要

腺苷酸活化蛋白激酶(AMPK)是分解代谢与合成代谢过程的关键调节剂。它作为能量传感器的特性使其能够将细胞的能量状态与代谢环境联系起来。这些适应性变化不仅通过直接磷酸化对关键代谢酶的急性调节发生,而且还通过较慢的转录适应性反应发生。AMPK 如何调节许多基因集的表达的问题,例如与线粒体生物发生、能量产生和氧化保护相关的基因集的表达,才刚刚开始被阐明,还有许多问题有待解答。在这篇综述中,我们将尝试整合我们目前关于 AMPK 如何调节肌肉和肝脏转录的知识,这将作为例证来说明该领域的主要进展和未来的关键挑战。