The ubiquitin proteasome system in neurodegenerative diseases: culprit, accomplice or victim?

Prog Neurobiol. 2012 Feb;96(2):190-207. doi: 10.1016/j.pneurobio.2012.01.003. Epub 2012 Jan 16.

Abstract

A shared hallmark for many neurodegenerative disorders is the accumulation of toxic protein species which is assumed to be the cause for these diseases. Since the ubiquitin proteasome system (UPS) is the most important pathway for selective protein degradation it is likely that it is involved in the aetiology neurodegenerative disorders. Indeed, impairment of the UPS has been reported to occur during neurodegeneration. Although accumulation of toxic protein species (amyloid β) are in turn known to impair the UPS the relationship is not necessarily causal. We provide an overview of the most recent insights in the roles the UPS plays in protein degradation and other processes. Additionally, we discuss the role of the UPS in clearance of the toxic proteins known to accumulate in the hallmarks of neurodegenerative diseases. The present paper will focus on critically reviewing the involvement of the UPS in specific neurodegenerative diseases and will discuss if UPS impairment is a cause, a consequence or both of the disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Humans
  • Models, Molecular
  • Neurodegenerative Diseases / metabolism*
  • Neurodegenerative Diseases / pathology
  • Neurodegenerative Diseases / physiopathology*
  • Proteasome Endopeptidase Complex / metabolism*
  • Protein Conformation
  • Proteolysis
  • Signal Transduction / physiology
  • Ubiquitin / chemistry
  • Ubiquitin / metabolism*
  • Ubiquitination

Substances

  • Ubiquitin
  • Proteasome Endopeptidase Complex