Lewy pathology in Parkinson's disease consists of crowded organelles and lipid membranes.
Alzheimer Disease
/ metabolism
Hippocampus
/ chemistry
Humans
Imaging, Three-Dimensional
Intracellular Membranes
/ ultrastructure
Lewy Bodies
/ chemistry
Lewy Body Disease
/ metabolism
Membrane Lipids
/ analysis
Mesencephalon
/ chemistry
Microscopy, Confocal
Microscopy, Electron
/ methods
Microscopy, Fluorescence
Organelles
/ ultrastructure
Parkinson Disease
/ metabolism
Substantia Nigra
/ chemistry
Exome Sequencing
alpha-Synuclein
/ analysis
Journal
Nature neuroscience
ISSN: 1546-1726
Titre abrégé: Nat Neurosci
Pays: United States
ID NLM: 9809671
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
26
10
2018
accepted:
09
05
2019
entrez:
26
6
2019
pubmed:
27
6
2019
medline:
19
7
2019
Statut:
ppublish
Résumé
Parkinson's disease, the most common age-related movement disorder, is a progressive neurodegenerative disease with unclear etiology. Key neuropathological hallmarks are Lewy bodies and Lewy neurites: neuronal inclusions immunopositive for the protein α-synuclein. In-depth ultrastructural analysis of Lewy pathology is crucial to understanding pathogenesis of this disease. Using correlative light and electron microscopy and tomography on postmortem human brain tissue from Parkinson's disease brain donors, we identified α-synuclein immunopositive Lewy pathology and show a crowded environment of membranes therein, including vesicular structures and dysmorphic organelles. Filaments interspersed between the membranes and organelles were identifiable in many but not all α-synuclein inclusions. Crowding of organellar components was confirmed by stimulated emission depletion (STED)-based super-resolution microscopy, and high lipid content within α-synuclein immunopositive inclusions was corroborated by confocal imaging, Fourier-transform coherent anti-Stokes Raman scattering infrared imaging and lipidomics. Applying such correlative high-resolution imaging and biophysical approaches, we discovered an aggregated protein-lipid compartmentalization not previously described in the Parkinsons' disease brain.
Identifiants
pubmed: 31235907
doi: 10.1038/s41593-019-0423-2
pii: 10.1038/s41593-019-0423-2
doi:
Substances chimiques
Membrane Lipids
0
alpha-Synuclein
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1099-1109Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM081653
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn