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J Biol Chem. 2011 Jun 24;286(25):22262-74. doi: 10.1074/jbc.M110.202937. Epub 2011 Apr 28.

Structural and morphological characterization of aggregated species of α-synuclein induced by docosahexaenoic acid.

Author information

1
Centro di Ricerca Interdipartimentale per Biotecnologie Innovative (Biotechnology Centre), University of Padova, Viale G. Colombo 3, 35121 Padova, Italy.

Abstract

The interaction of brain lipids with α-synuclein may play an important role in the pathogenesis of Parkinson disease (PD). Docosahexaenoic acid (DHA) is an abundant fatty acid of neuronal membranes, and it is presents at high levels in brain areas with α-synuclein inclusions of patients with PD. In animal models, an increase of DHA content in the brain induces α-synuclein oligomer formation in vivo. However, it is not clear whether these oligomeric species are the precursors of the larger aggregates found in Lewy bodies of post-mortem PD brains. To characterize these species and to define the role of fatty acids in amyloid formation, we investigated the aggregation process of α-synuclein in the presence of DHA. We found that DHA readily promotes α-synuclein aggregation and that the morphology of these aggregates is dependent on the ratio between the protein and DHA. In the presence of a molar ratio protein/DHA of 1:10, amyloid-like fibrils are formed. These fibrils are morphologically different from those formed by α-synuclein alone and have a less packed structure. At a protein/DHA molar ratio of 1:50, we observe the formation of stable oligomers. Moreover, chemical modifications, methionine oxidations, and protein-lipid adduct formations are induced by increasing concentrations of DHA. The extent of these modifications defines the structure and the stability of aggregates. We also show that α-synuclein oligomers are more toxic if generated in the presence of DHA in dopaminergic neuronal cell lines, suggesting that these species might be important in the neurodegenerative process associated with PD.

PMID:
21527634
PMCID:
PMC3121372
DOI:
10.1074/jbc.M110.202937
[Indexed for MEDLINE]
Free PMC Article

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