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Updated: Jun 10, 2026

Studying Pre-formed Fibril Induced α-Synuclein Accumulation in Primary Embryonic Mouse Midbrain Dopamine Neurons
Published on: August 16, 2020
Ultrastructural diversity and subcellular organization of nigral Lewy pathology in Parkinson's disease
Amanda J Lewis1,2, Lukas van den Heuvel3,4, Marta Di Fabrizio3,4
1Laboratory of Biological Electron Microscopy, School of Basic Sciences, Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland. amanda.lewis@epfl.ch.
Abstract:
Lewy bodies, the defining pathological feature of Parkinson's disease, are intraneuronal inclusions enriched in aggregated alpha-synuclein (αSyn). We used correlative light and electron microscopy to selectively investigate phosphorylated αSyn (αSynpS129)-positive inclusions in the substantia nigra of end-stage postmortem Parkinson's disease brain. Here we show that somatic αSynpS129 inclusions in nigral dopaminergic neurons are consistently fibrillar, whereas the membranous-type inclusions are restricted to neuritic processes. These neuritic inclusions displayed marked ultrastructural heterogeneity, ranging from predominantly membranous to mixed membranous-fibrillar forms. The selective targeting of defined inclusions enabled detailed structural characterization of Lewy pathology, rather than quantitative or disease-stage comparisons. Our findings highlight clear ultrastructural differences between somatic and neuritic αSynpS129 pathology and demonstrate the structural complexity and heterogeneity of Lewy pathology in human Parkinson's disease brain.
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