The Tangled Circuitry of Metabolism and Apoptosis

被引:91
作者
Andersen, Joshua L. [1 ]
Kornbluth, Sally [2 ]
机构
[1] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
[2] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
PROMOTES CELL-SURVIVAL; BCL-2 PROTEIN FAMILY; CYTOCHROME-C; MITOCHONDRIAL FISSION; OXIDATIVE STRESS; MEMBRANE PERMEABILIZATION; CASPASE-2-DEFICIENT MICE; P53-INDUCIBLE REGULATOR; TRANSCRIPTION FACTORS; GLUCOSE TRANSPORTERS;
D O I
10.1016/j.molcel.2012.12.026
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
For single-cell organisms, nutrient uptake and metabolism are central to the fundamental decision of whether to grow or divide. In metazoans, cell fate decisions are more complex: organismal homeostasis must be strictly maintained by balancing cell proliferation and death. Despite this increased complexity, cell fate within multicellular organisms is also influenced by metabolism; recent studies, triggered in part by an interest in tumor metabolism, are beginning to illuminate the mechanisms through which proliferation, death, and metabolism are intertwined. In particular, work on Bcl-2 family proteins suggests that the signaling pathways governing metabolism and apoptosis are inextricably linked. Here we review the crosstalk between these pathways, emphasizing recent work that illustrates the emerging dual nature of several core apoptotic proteins in regulating both metabolism and cell death.
引用
收藏
页码:399 / 410
页数:12
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