Department of Physiology and Medical Physics, RCSI Neuroscience Research Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.
Antioxid Redox Signal. 2011 May 15;14(10):1863-76. doi: 10.1089/ars.2010.3544. Epub 2011 Feb 18.
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 Ca(2+) 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.
5'-腺苷一磷酸(AMP)激活的蛋白激酶(AMPK)是细胞能量状态的关键传感器。AMPK 信号通路调节细胞、器官和全身水平的能量平衡。最近,人们已经清楚地认识到,AMPK 还在决定细胞命运的长期决策中发挥着重要作用,特别是细胞周期进展和细胞凋亡的激活。在这里,我们描述了 AMPK 激活的多种机制以及 AMPK 在调节细胞能量平衡中的作用。我们总结了最近的研究表明,AMPK 激活参与了神经元存活的调节,并且在缺血性中风中是一个关键的参与者。我们还提出,AMPK 激活在调节神经元存活方面可能具有双重功能:AMPK 在神经元 Ca(2+)超载模型中所代表的短暂能量耗竭期间提供保护作用,这种作用部分是通过神经元葡萄糖转运蛋白 3 的激活介导的。相反,长期的 AMPK 激活可通过转录激活促凋亡 Bcl-2 家族成员 bim 导致神经元凋亡。讨论了决定 AMPK 激活的保护作用与细胞死亡诱导作用的分子开关。