In vivo demonstration that α-synuclein oligomers are toxic
Salk Institute for Biological Studies · Friedrich-Alexander-Universität Erlangen-Nürnberg · +3 more institutions
Abstract
The aggregation of proteins into oligomers and amyloid fibrils is characteristic of several neurodegenerative diseases, including Parkinson disease (PD). In PD, the process of aggregation of α-synuclein (α-syn) from monomers, via oligomeric intermediates, into amyloid fibrils is considered the disease-causative toxic mechanism. We developed α-syn mutants that promote oligomer or fibril formation and tested the toxicity of these mutants by using a rat lentivirus system to investigate loss of dopaminergic neurons in the substantia nigra. The most severe dopaminergic loss in the substantia nigra is observed in animals with the α-syn variants that form oligomers (i.e., E57K and E35K), whereas the α-syn variants…
Citation impact
- FWCI
- 49.19
- Percentile
- 100%
- References
- 35
Authors
19- BWBeate WinnerCorresponding
Salk Institute for Biological Studies, Friedrich-Alexander-Universität Erlangen-Nürnberg
- RJRoberto Jappelli
Salk Institute for Biological Studies
- SKSamir K. Maji
Board of the Swiss Federal Institutes of Technology, ETH Zurich
- PDPaula Desplats
University of California San Diego
- LBLeah Boyer
Salk Institute for Biological Studies, University of California San Diego
Topics & keywords
- Fibril
- Substantia nigra
- Oligomer
- Alpha-synuclein
- Chemistry
- Mutant
- In vivo
- Amyloid (mycology)