bioRxivNeurosciencePreprint
Subcellular orchestration of alpha-synuclein variants in Parkinson’s disease brains revealed by 3D multicolor STED microscopy
Tim E. MoorsiD, Christina A. MaatiD, Daniel NiediekeriD, Daniel Mona, Dennis Petersen, Evelien Huisman, Jeroen Kole, Samir F. El-Mashtoly, Liz Spycher, Wagner Zago, Robin Barbour, Olaf Mundigl, Klaus Kaluza, Sylwia Huber, Melanie N. Hug, Thomas Kremer, Mirko Ritter, Sebastian Dziadek, Jeroen J.G. GeurtsiD, Klaus Gerwert, Markus BritschgiiD, Wilma D. J. van de BergiD
Abstract
Post-translational modifications of alpha-synuclein (aSyn), particularly phosphorylation at Serine 129 (Ser129-p) and truncation of its C-terminus (CTT), have been implicated in Parkinsons disease (PD) pathology. To gain more insight in the relevance of Ser129-p and CTT aSyn under physiological and pathological conditions, we investigated their subcellular distribution patterns in normal aged and PD brains using highly-selective antibodies in combination with 3D multicolor STED microscopy. We show that CTT aSyn localizes in mitochondria in PD patients and controls, whereas the organization of Ser129-p in a cytoplasmic network is strongly associated with pathology. Nigral Lewy bodies show an onion skin-like architecture, with a structured framework of Ser129-p aSyn and neurofilaments encapsulating CTT aSyn in their core, which displayed high content of proteins and lipids by label-free CARS microscopy. The subcellular phenotypes of antibody-labeled pathology identified in this study provide evidence for a crucial role of Ser129-p aSyn in Lewy body formation.
- organism: human
- assay: imaging
- research focus: cell type annotation
- research focus: spatial domain detection
- approach: experimental assay
- Citations
- 28
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Prominent astrocytic alpha-synuclein pathology with unique post-translational modification signatures unveiled across Lewy body disorders
Melek Firat Altay, Alan King Lun Liu, … Hilal Ahmed Lashuel·Acta Neuropathologica CommunicationsPeer-reviewed·Nov 12, 2022
- Neighbouring modifications interfere with the detection of phosphorylated alpha-synuclein at Serine 129: Revisiting the specificity of pS129 antibodies
Hilal Ahmed Lashuel, Anne‐Laure Mahul‐Mellier, … Nicolas Guex·bioRxiv·Mar 30, 2022
- Ultrastructural diversity and subcellular organization of nigral Lewy pathology in Parkinson's disease
Amanda J. Lewis, Lukas van den Heuvel, … Henning Stahlberg·Nature CommunicationsPeer-reviewed·Jun 8, 2026
- Dissecting the differential role of C-terminal truncations in the regulation of aSyn pathology formation and the biogenesis of Lewy bodies
Anne‐Laure Mahul‐Mellier, Melek Firat Altay, … Hilal Ahmed Lashuel·bioRxiv·Nov 29, 2024
- Linking acetylated alpha-Tubulin redistribution to alpha-Synuclein pathology in brain of Parkinson's disease patients
Samanta Mazzetti, Federica Giampietro, … Graziella Cappelletti·npj Parkinson s DiseasePeer-reviewed·Jan 2, 2024
- Pathological relevance of post-translationally modified alpha-synuclein (pSer87, pSer129, nTyr39) in idiopathic Parkinson's disease and Multiple System Atrophy.
Berkiye Sonustun, Melek Firat Altay, … Rina Bandopadhyay·CellsPeer-reviewed·Mar 6, 2022