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Alpha-synuclein mediates alterations in membrane conductance: a potential role for alpha-synuclein oligomers in cell vulnerability.
- Source :
-
The European journal of neuroscience [Eur J Neurosci] 2010 Jul; Vol. 32 (1), pp. 10-7. Date of Electronic Publication: 2010 Jun 14. - Publication Year :
- 2010
-
Abstract
- alpha-Synuclein has been linked to the pathogenesis of Parkinson's disease and other synucleinopathies through its propensity to form toxic oligomers. The exact mechanism for oligomeric synuclein-directed cell vulnerability has not been fully elucidated, but one hypothesis portends the formation of synuclein-containing pores within cell membranes leading to leak channel-mediated calcium influx and subsequent cell death. Here we demonstrate synuclein-induced formation of sodium dodecyl sulfate-stable oligomers, intracellular synuclein-positive aggregates, alterations in membrane conductance reminiscent of leak channels and subsequent cytotoxicity in a dopaminergic-like cell line. Furthermore we demonstrate that the synuclein-induced membrane conductance changes are blocked by direct extracellular application of an anti-synuclein antibody. The work presented here confirms that synuclein overexpression leads to membrane conductance changes and demonstrates for the first time through antibody-blocking studies that synuclein plays a direct role in the formation of leak channels.
- Subjects :
- Animals
Cell Line
Cell Membrane chemistry
Dopamine metabolism
Electric Conductivity
Humans
Mice
Patch-Clamp Techniques
Potassium Channels, Tandem Pore Domain metabolism
alpha-Synuclein genetics
Cell Death physiology
Cell Membrane metabolism
Neurons metabolism
Protein Multimerization
alpha-Synuclein chemistry
alpha-Synuclein metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1460-9568
- Volume :
- 32
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The European journal of neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 20550572
- Full Text :
- https://doi.org/10.1111/j.1460-9568.2010.07266.x