线粒体
细胞生物学
程序性细胞死亡
自噬
生物能学
细胞器
生物
细胞代谢
细胞命运测定
氧化磷酸化
代谢途径
细胞凋亡
细胞
新陈代谢
生物化学
转录因子
基因
作者
Douglas R. Green,Lorenzo Galluzzi,Guido Kroemer
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2014-09-18
卷期号:345 (6203)
被引量:572
标识
DOI:10.1126/science.1250256
摘要
Beyond their contribution to basic metabolism, the major cellular organelles, in particular mitochondria, can determine whether cells respond to stress in an adaptive or suicidal manner. Thus, mitochondria can continuously adapt their shape to changing bioenergetic demands as they are subjected to quality control by autophagy, or they can undergo a lethal permeabilization process that initiates apoptosis. Along similar lines, multiple proteins involved in metabolic circuitries, including oxidative phosphorylation and transport of metabolites across membranes, may participate in the regulated or catastrophic dismantling of organelles. Many factors that were initially characterized as cell death regulators are now known to physically or functionally interact with metabolic enzymes. Thus, several metabolic cues regulate the propensity of cells to activate self-destructive programs, in part by acting on nutrient sensors. This suggests the existence of "metabolic checkpoints" that dictate cell fate in response to metabolic fluctuations. Here, we discuss recent insights into the intersection between metabolism and cell death regulation that have major implications for the comprehension and manipulation of unwarranted cell loss.
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