Lewy-like aggregation of α-synuclein reduces protein phosphatase 2A activity in vitro and in vivo

Neuroscience. 2012 Apr 5:207:288-97. doi: 10.1016/j.neuroscience.2012.01.028. Epub 2012 Jan 25.

Abstract

α-synuclein (α-Syn) is a chaperone-like protein that is highly implicated in Parkinson's disease (PD) as well as in dementia with Lewy bodies (DLB). Rare forms of PD occur in individuals with mutations of α-Syn or triplication of wild type α-Syn, and in both PD and DLB the intraneuronal inclusions known as Lewy bodies contain aggregated α-Syn that is highly phosphorylated on serine 129. In neuronal cells and in the brains of α-Syn overexpressing transgenic mice, soluble α-Syn stimulates the activity of protein phosphatase 2A (PP2A), a major serine/threonine phosphatase. Serine 129 phosphorylation of α-Syn attenuates its stimulatory effects on PP2A and also accelerates α-Syn aggregation; however, it is unknown if aggregation of α-Syn into Lewy bodies impairs PP2A activity. To assess for this, we measured the impact of α-Syn aggregation on PP2A activity in vitro and in vivo. In cell-free assays, aggregated α-Syn had ∼50% less PP2A stimulatory effects than soluble recombinant α-Syn. Similarly in DLB and α-Syn triplication brains, which contain robust α-Syn aggregation with high levels of serine 129 phosphorylation, PP2A activity was also ∼50% attenuated. As α-Syn normally stimulates PP2A activity, our data suggest that overexpression of α-Syn or sequestration of α-Syn into Lewy bodies has the potential to alter the phosphorylation state of key PP2A substrates; raising the possibility that all forms of synucleinopathy will benefit from treatments aimed at optimizing PP2A activity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Brain / enzymology
  • Brain / metabolism
  • Brain / pathology
  • Down-Regulation / physiology
  • Female
  • Frontal Lobe / enzymology
  • Frontal Lobe / metabolism*
  • Frontal Lobe / pathology
  • Humans
  • Lewy Bodies / enzymology
  • Lewy Bodies / metabolism*
  • Lewy Bodies / pathology
  • Lewy Body Disease / enzymology
  • Lewy Body Disease / metabolism*
  • Lewy Body Disease / pathology
  • Male
  • Middle Aged
  • Parkinson Disease / enzymology
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology
  • Protein Phosphatase 2 / antagonists & inhibitors*
  • Protein Phosphatase 2 / metabolism
  • Substrate Specificity / physiology
  • alpha-Synuclein / chemistry
  • alpha-Synuclein / metabolism
  • alpha-Synuclein / physiology*

Substances

  • SNCA protein, human
  • alpha-Synuclein
  • Protein Phosphatase 2