alpha-Synuclein interacts with phospholipase D isozymes and inhibits pervanadate-induced phospholipase D activation in human embryonic kidney-293 cells

J Biol Chem. 2002 Apr 5;277(14):12334-42. doi: 10.1074/jbc.M110414200. Epub 2002 Jan 30.

Abstract

alpha-Synuclein has been implicated in the pathogenesis of many neurodegenerative diseases, including Parkinson's disease and Alzheimer's disease. Although the function of alpha-synuclein remains largely unknown, recent studies have demonstrated that this protein can interact with phospholipids. To address the role of alpha-synuclein in neurodegenerative disease, we have investigated whether it binds phospholipase D (PLD) and affects PLD activity in human embryonic kidney (HEK)-293 cells overexpressing wild type alpha-synuclein or the mutant forms of alpha-synuclein (A53T, A30P) associated with Parkinson's disease. Tyrosine phosphorylation of alpha-synuclein appears to play a modulatory role in the inhibition of PLD, because mutation of Tyr(125) to Phe slightly increases inhibitory effect of alpha-synuclein on PLD activity. Treatment with pervanadate or phorbol myristate acetate inhibits PLD more in HEK 293 cells overexpressing alpha-synuclein than in control cells. Binding of alpha-synuclein to PLD requires phox and pleckstrin homology domain of PLD and the amphipathic repeat region and non-Abeta component of alpha-synuclein. Although biologically important, co-transfection studies indicate that the interaction of alpha-synuclein with PLD does not influence the tendency of alpha-synuclein to form pathological inclusions. These results suggest that the association of alpha-synuclein with PLD, and modulation of PLD activity, is biologically important, but PLD does not appear to play an essential role in the pathophysiology of alpha-synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Proteins / chemistry
  • Blotting, Western
  • Brain / metabolism
  • Cell Line
  • Cytoplasm / metabolism
  • DNA, Complementary / metabolism
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Eosinophils / metabolism
  • Glutathione Transferase / metabolism
  • Humans
  • Microscopy, Fluorescence
  • Mutation
  • Nerve Tissue Proteins / chemistry*
  • Nerve Tissue Proteins / metabolism*
  • Phospholipase D / chemistry*
  • Phospholipase D / metabolism
  • Phosphoproteins / chemistry
  • Phosphorylation
  • Precipitin Tests
  • Protein Binding
  • Protein Isoforms
  • Protein Structure, Tertiary
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Synucleins
  • Tetradecanoylphorbol Acetate / pharmacology
  • Time Factors
  • Transfection
  • Tyrosine / metabolism
  • Vanadates / pharmacology*
  • alpha-Synuclein

Substances

  • Blood Proteins
  • DNA, Complementary
  • Enzyme Inhibitors
  • Nerve Tissue Proteins
  • Phosphoproteins
  • Protein Isoforms
  • Recombinant Fusion Proteins
  • SNCA protein, human
  • Snca protein, rat
  • Synucleins
  • alpha-Synuclein
  • pervanadate
  • platelet protein P47
  • Vanadates
  • Tyrosine
  • Glutathione Transferase
  • Phospholipase D
  • Tetradecanoylphorbol Acetate