| Literature DB >> 31235907 |
Sarah H Shahmoradian1,2, Amanda J Lewis1, Christel Genoud3, Jürgen Hench4, Tim E Moors5, Paula P Navarro1, Daniel Castaño-Díez1, Gabriel Schweighauser4, Alexandra Graff-Meyer3, Kenneth N Goldie1, Rosmarie Sütterlin1, Evelien Huisman5, Angela Ingrassia5, Yvonne de Gier5, Annemieke J M Rozemuller6, Jing Wang1, Anne De Paepe7, Johannes Erny8, Andreas Staempfli8, Joerg Hoernschemeyer8, Frederik Großerüschkamp9, Daniel Niedieker9, Samir F El-Mashtoly9, Marialuisa Quadri10, Wilfred F J Van IJcken11, Vincenzo Bonifati10, Klaus Gerwert9, Bernd Bohrmann12, Stephan Frank4, Markus Britschgi12, Henning Stahlberg13, Wilma D J Van de Berg14, Matthias E Lauer15.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2019 PMID: 31235907 DOI: 10.1038/s41593-019-0423-2
Source DB: PubMed Journal: Nat Neurosci ISSN: 1097-6256 Impact factor: 24.884