| Literature DB >> 31064841 |
Cathryn L Ugalde1,2,3,4, Victoria A Lawson2, David I Finkelstein3, Andrew F Hill5,4.
Abstract
The misfolding and aggregation of α-synuclein (αsyn) in the central nervous system is associated with a group of neurodegenerative disorders referred to as the synucleinopathies. In addition to being a pathological hallmark of disease, it is now well-established that upon misfolding, αsyn acquires pathogenic properties, such as neurotoxicity, that can contribute to disease development. The mechanisms that produce αsyn misfolding and the molecular events underlying the neuronal damage caused by these misfolded species are not well-defined. A consistent observation that may be relevant to αsyn's pathogenicity is its ability to associate with lipids. This appears important not only to how αsyn aggregates, but also to the mechanism by which the misfolded protein causes intracellular damage. This review discusses the current literature reporting a role of lipids in αsyn misfolding and neurotoxicity in various synucleinopathy disorders and provides an overview of current methods to assess protein misfolding and pathogenicity both in vitro and in vivo.Entities:
Keywords: Lewy body; Parkinson disease; alpha-synuclein; amyloid; lipid; mitochondrial function; neurodegeneration; neurodegenerative disease; neurotoxicity; protein misfolding; synucleinopathy
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Year: 2019 PMID: 31064841 PMCID: PMC6556586 DOI: 10.1074/jbc.REV119.007500
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157