FABP3 protein promotes α-synuclein oligomerization associated with 1-methyl-1,2,3,6-tetrahydropiridine-induced neurotoxicity

J Biol Chem. 2014 Jul 4;289(27):18957-65. doi: 10.1074/jbc.M113.527341. Epub 2014 May 22.

Abstract

α-Synuclein (αSyn) accumulation in dopaminergic (DA) neurons is partly regulated by long-chain polyunsaturated fatty acids. We found that fatty acid-binding protein 3 (FABP3, H-FABP), a factor critical for arachidonic acid (AA) transport and metabolism in brain, is highly expressed in DA neurons. Fabp3 knock-out (Fabp3(-/-)) mice were resistant to 1-methyl-1,2,3,6-tetrahydropiridine-induced DA neurodegeneration in the substantia nigra pars compacta and showed improved motor function. Interestingly, FABP3 interacted with αSyn in the substantia nigra pars compacta, and αSyn accumulation following 1-methyl-1,2,3,6-tetrahydropiridine treatment was attenuated in Fabp3(-/-) compared with wild-type mice. We confirmed that FABP3 overexpression aggravates AA-induced αSyn oligomerization and promotes cell death in PC12 cells, whereas overexpression of a mutant form of FABP3 lacking fatty-acid binding capacity did not. Taken together, αSyn oligomerization in DA neurons is likely aggravated by AA through FABP3 in Parkinson disease pathology.

Keywords: Cell Death; Dopamine; Dopaminergic Neuron; Fatty Acid-binding Protein; Fatty Acid-binding Protein 3; Parkinson Disease; Polyunsaturated Fatty Acid (PUFA); α-Synuclein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine*
  • Animals
  • Arachidonic Acid / pharmacology
  • Cell Death / drug effects
  • Dopaminergic Neurons / drug effects*
  • Dopaminergic Neurons / metabolism
  • Fatty Acid Binding Protein 3
  • Fatty Acid-Binding Proteins / deficiency
  • Fatty Acid-Binding Proteins / metabolism*
  • Gene Expression Regulation / drug effects
  • Humans
  • Kinetics
  • MPTP Poisoning / metabolism*
  • MPTP Poisoning / pathology
  • MPTP Poisoning / physiopathology
  • Mice
  • Motor Activity / drug effects
  • Neostriatum / cytology
  • Neurotoxins / toxicity*
  • PC12 Cells
  • Protein Binding
  • Protein Multimerization* / drug effects
  • Protein Structure, Quaternary
  • Rats
  • Substantia Nigra / cytology
  • alpha-Synuclein / chemistry*
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism

Substances

  • Fabp3 protein, mouse
  • Fatty Acid Binding Protein 3
  • Fatty Acid-Binding Proteins
  • Neurotoxins
  • alpha-Synuclein
  • Arachidonic Acid
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine