Danzer, Karin M.;
Haasen, Dorothea;
Karow, Anne R.;
Moussaud, Simon;
Habeck, Matthias;
Giese, Armin;
Kretzschmar, Hans;
Hengerer, Bastian;
Kostka, Marcus
Different Species of α-Synuclein Oligomers Induce Calcium Influx and Seeding
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Medientyp:
E-Artikel
Titel:
Different Species of α-Synuclein Oligomers Induce Calcium Influx and Seeding
Beteiligte:
Danzer, Karin M.;
Haasen, Dorothea;
Karow, Anne R.;
Moussaud, Simon;
Habeck, Matthias;
Giese, Armin;
Kretzschmar, Hans;
Hengerer, Bastian;
Kostka, Marcus
Erschienen:
Society for Neuroscience, 2007
Erschienen in:
The Journal of Neuroscience, 27 (2007) 34, Seite 9220-9232
Sprache:
Englisch
DOI:
10.1523/jneurosci.2617-07.2007
ISSN:
0270-6474;
1529-2401
Entstehung:
Anmerkungen:
Beschreibung:
Aggregation of α-synuclein (α-syn) has been linked to the pathogenesis of Parkinson's disease (PD) and other neurodegenerative diseases. Increasing evidence suggests that prefibrillar oligomers and protofibrils, rather than mature fibrils of α-syn, are the pathogenic species in PD. Despite extensive effort on studying oligomerization of α-syn, no studies have compared different oligomer species directly on a single-particle level and investigated their biological effects on cells. In this study, we applied a novel highly sensitive single molecule detection system that allowed a direct comparison of different oligomer types. Furthermore, we studied biological effects of different oligomer types on cells. For this purpose, we developed new oligomerization protocols, that enabled the use of these different oligomers in cell culture. We found that all of our three aggregation protocols resulted in heterogeneous populations of oligomers. Some types of oligomers induced cell death via disruption of cellular ion homeostasis by a presumably pore-forming mechanism. Other oligomer types could directly enter the cell resulting in increased α-syn aggregation. Based on our results, we propose that under various physiological conditions, heterogeneous populations of oligomeric forms will coexist in an equilibrium. These different oligomer types lead directly or indirectly to cell damage. Our data indicate that inhibition of early α-syn aggregation events would consequently prevent all α-syn oligomer related toxicities. This has important implications for the development of disease-modifying drugs for the treatment of PD and other synucleinopathies.