The nuclear accumulation of alpha-synuclein is mediated by importin alpha and promotes neurotoxicity by accelerating the cell cycle

Neuropharmacology. 2014 Jul:82:132-42. doi: 10.1016/j.neuropharm.2013.07.035. Epub 2013 Aug 21.

Abstract

α-Synuclein (α-syn), a 14 kDa pre-synaptic protein, is widely involved in the Parkinson's disease (PD) pathogenesis. Recent studies have shown that the nuclear accumulation of α-syn might have a toxic effect. The main purpose of the present study was to explore which amino acid residues in α-syn are associated with its nuclear accumulation, the molecule(s) mediated the nuclear import of α-syn, and the role of α-syn accumulated in the nucleus. It has been noted that the nuclear import of α-syn may be mediated by importin α and that both the amino acid residues 1-60 and 103-140 of α-syn were indispensable for its nuclear import. After imported into the nucleus, the accumulated α-syn played a toxic role in both the PC12 cells and the C57 mice. Furthermore, α-syn-nuclear localization signal-injected mice showed behavioral symptoms associated with PD. Further studies performed in vitro showed that the toxicity of α-syn in the nucleus might be due to an interference of the cell cycle. Thus, it can be concluded that α-syn can accumulate in nucleus, which is mediated by importin α, and promote neurotoxicity by accelerating the cell cycle.

Keywords: Cell cycle; Importin α; Neurotoxicity; Nuclear accumulation; α-Synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / drug effects
  • Active Transport, Cell Nucleus / physiology
  • Animals
  • Behavior, Animal / physiology
  • Cell Cycle / drug effects
  • Cell Cycle / physiology*
  • Cell Nucleus / drug effects
  • Cell Nucleus / physiology*
  • Dopaminergic Neurons / diagnostic imaging
  • Dopaminergic Neurons / physiology
  • Glucose / metabolism
  • Mice, Inbred C57BL
  • Neurotoxicity Syndromes / physiopathology
  • PC12 Cells
  • Radionuclide Imaging
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Rotenone / toxicity
  • Substantia Nigra / diagnostic imaging
  • Substantia Nigra / physiopathology
  • Transfection
  • Uncoupling Agents / toxicity
  • alpha Karyopherins / metabolism*
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism*

Substances

  • Recombinant Fusion Proteins
  • SNCA protein, human
  • Snca protein, mouse
  • Uncoupling Agents
  • alpha Karyopherins
  • alpha-Synuclein
  • Rotenone
  • Glucose