Are aberrant phase transitions a driver of cellular aging?

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Simon Alberti - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)
  • Anthony A. Hyman - , Max Planck Institute of Molecular Cell Biology and Genetics (Author)

Abstract

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.

Details

Original languageEnglish
Pages (from-to)959-968
Number of pages10
JournalBIOESSAYS
Volume38
Issue number10
Publication statusPublished - 1 Oct 2016
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 27554449
ORCID /0000-0003-4017-6505/work/142253871

Keywords

Keywords

  • aging, amyotrophic lateral sclerosis, chaperone, intrinsically disordered protein, mitochondria, neurodegeneration, phase separation, protein aggregation, protein quality control

Library keywords