Are aberrant phase transitions a driver of cellular aging?

被引:219
作者
Alberti, Simon [1 ]
Hyman, Anthony A. [1 ]
机构
[1] Max Planck Inst Mol Cell Biol & Genet, Dresden, Germany
关键词
aging; amyotrophic lateral sclerosis; chaperone; intrinsically disordered protein; mitochondria; neurodegeneration; phase separation; protein aggregation; protein quality control; AMYOTROPHIC-LATERAL-SCLEROSIS; RNA-BINDING PROTEINS; PRION-LIKE DOMAINS; INTRINSICALLY DISORDERED PROTEINS; LOW-COMPLEXITY DOMAINS; NUCLEOCYTOPLASMIC TRANSPORT; NEURODEGENERATIVE DISEASES; STRESS GRANULES; LIQUID DROPLETS; SARCOMA FUS;
D O I
10.1002/bies.201600042
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Why do cells age? Recent advances show that the cytoplasm is organized into many membrane-less compartments via a process known as phase separation, which ensures spatiotemporal control over diffusion-limited biochemical reactions. Although phase separation is a powerful mechanism to organize biochemical reactions, it comes with the trade-off that it is extremely sensitive to changes in physical-chemical parameters, such as protein concentration, pH, or cellular energy levels. Here, we highlight recent findings showing that age-related neurodegenerative diseases are linked to aberrant phase transitions in neurons. We discuss how these aberrant phase transitions could be tied to a failure to maintain physiological physical-chemical conditions. We generalize this idea to suggest that the process of cellular aging involves a progressive loss of the organization of phase-separated compartments in the cytoplasm.
引用
收藏
页码:959 / 968
页数:10
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