Role of 5′-Adenosine Monophosphate-Activated Protein Kinase in Cell Survival and Death Responses in Neurons

被引:67
作者
Weisova, Petronela [1 ]
Davila, David [1 ]
Tuffy, Liam P. [1 ]
Ward, Manus W. [1 ]
Concannon, Caoimhin G. [1 ]
Prehn, Jochen H. M. [1 ]
机构
[1] Royal Coll Surgeons Ireland, RCSI Neurosci Res Ctr, Dept Physiol & Med Phys, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
N-TERMINAL KINASE; AMP-KINASE; MITOCHONDRIAL DYSFUNCTION; GLUTAMATE EXCITOTOXICITY; ADENOSINE-MONOPHOSPHATE; MEDIATED ACTIVATION; METABOLIC STRESS; ENERGY DEPLETION; UPSTREAM KINASE; SKELETAL-MUSCLE;
D O I
10.1089/ars.2010.3544
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
5'-Adenosine monophosphate (AMP)-activated protein kinase (AMPK) is a key sensor of cellular energy status. AMPK signaling regulates energy balance at the cellular, organ, and whole-body level. More recently, it has become apparent that AMPK plays also an important role in long-term decisions that determine cell fate, in particular cell cycle progression and apoptosis activation. Here, we describe the diverse mechanisms of AMPK activation and the role of AMPK in the regulation of cellular energy balance. We summarize recent studies implicating AMPK activation in the regulation of neuronal survival and as a key player during ischemic stroke. We also suggest that AMPK activation may have dual functions in the regulation of neuronal survival: AMPK provides a protective effect during transient energy depletion as exemplified in a model of neuronal Ca2+ overloading, and this effect is partially mediated by the activation of neuronal glucose transporter 3. Prolonged AMPK activation, on the contrary, can lead to neuronal apoptosis via the transcriptional activation of the proapoptotic Bcl-2 family member, bim. Molecular switches that determine the protective versus cell death-inducing effects of AMPK activation are discussed. Antioxid. Redox Signal. 14, 1863-1876.
引用
收藏
页码:1863 / 1876
页数:14
相关论文
共 124 条
[1]   Glutamate neurotoxicity is associated with nitric oxide-mediated mitochondrial dysfunction and glutathione depletion [J].
Almeida, A ;
Heales, SJR ;
Bolaños, JP ;
Medina, JM .
BRAIN RESEARCH, 1998, 790 (1-2) :209-216
[2]   Nitric oxide switches on glycolysis through the AMP protein kinase and 6-phosphofructo-2-kinase pathway [J].
Almeida, A ;
Moncada, S ;
Bolaños, JP .
NATURE CELL BIOLOGY, 2004, 6 (01) :45-U9
[3]   Hypothalamic CaMKK2 contributes to the regulation of energy balance [J].
Anderson, Kristin A. ;
Ribar, Thomas J. ;
Lin, Fumin ;
Noeldner, Pamela K. ;
Green, Michelle F. ;
Muehlbauer, Michael J. ;
Witters, Lee A. ;
Kemp, Bruce E. ;
Means, Anthony R. .
CELL METABOLISM, 2008, 7 (05) :377-388
[4]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[5]   AMP-activated protein kinase in the heart - Role during health and disease [J].
Arad, Michael ;
Seidman, Christine E. ;
Seidman, J. G. .
CIRCULATION RESEARCH, 2007, 100 (04) :474-488
[6]   Rapid uncoupling of oxidative phosphorylation accompanies glutamate toxicity in rat cerebellar granule cells [J].
Atlante, A ;
Gagliardi, S ;
Minervini, GM ;
Marra, E ;
Passarella, S ;
Calissano, P .
NEUROREPORT, 1996, 7 (15-17) :2519-2523
[7]   Resveratrol improves health and survival of mice on a high-calorie diet [J].
Baur, Joseph A. ;
Pearson, Kevin J. ;
Price, Nathan L. ;
Jamieson, Hamish A. ;
Lerin, Carles ;
Kalra, Avash ;
Prabhu, Vinayakumar V. ;
Allard, Joanne S. ;
Lopez-Lluch, Guillermo ;
Lewis, Kaitlyn ;
Pistell, Paul J. ;
Poosala, Suresh ;
Becker, Kevin G. ;
Boss, Olivier ;
Gwinn, Dana ;
Wang, Mingyi ;
Ramaswamy, Sharan ;
Fishbein, Kenneth W. ;
Spencer, Richard G. ;
Lakatta, Edward G. ;
Le Couteur, David ;
Shaw, Reuben J. ;
Navas, Placido ;
Puigserver, Pere ;
Ingram, Donald K. ;
de Cabo, Rafael ;
Sinclair, David A. .
NATURE, 2006, 444 (7117) :337-342
[8]   Deranged neuronal calcium signaling and Huntington disease [J].
Bezprozvanny, I ;
Hayden, MR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 322 (04) :1310-1317
[9]   Pro-apoptotic Bim induction in response to nerve growth factor deprivation requires simultaneous activation of three different death signaling pathways [J].
Biswas, Subhas C. ;
Shi, Yijie ;
Sproul, Andrew ;
Greene, Lloyd A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (40) :29368-29374
[10]   AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. [J].
Bolster, DR ;
Crozier, SJ ;
Kimball, SR ;
Jefferson, LS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (27) :23977-23980