Autor: |
Danzer KM; CNS Research Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany. kdanzer@partners.org, Krebs SK, Wolff M, Birk G, Hengerer B |
Jazyk: |
angličtina |
Zdroj: |
Journal of neurochemistry [J Neurochem] 2009 Oct; Vol. 111 (1), pp. 192-203. Date of Electronic Publication: 2009 Aug 04. |
DOI: |
10.1111/j.1471-4159.2009.06324.x |
Abstrakt: |
Lewy bodies, alpha-synuclein (alpha-syn) immunopositive intracellular deposits, are the pathological hallmark of Parkinson's disease (PD). Interestingly, Lewybody-like structures have been identified in fetal tissue grafts about one decade after transplantation into the striatum of PD patients. One possible explanation for the accelerated deposition of alpha-syn in the graft is that the aggregation of alpha-syn from the host tissue to the graft is spread by a prion disease-like mechanism. We discuss here an in vitro model which might recapitulate some aspects of disease propagation in PD. We found here that in vitro-generated alpha-syn oligomers induce transmembrane seeding of alpha-syn aggregation in a dose- and time-dependent manner. This effect was observed in primary neuronal cultures as well as in neuronal cell lines. The seeding oligomers were characterized by a distinctive lithium dodecyl sulfate-stable oligomer pattern and could be generated in a dynamic process out of pore-forming oligomers. We propose that alpha-syn oligomers form as a dynamic mixture of oligomer types with different properties and that alpha-syn oligomers can be converted into different types depending on the brain milieu conditions. Our data indicate that extracellular alpha-syn oligomers can induce intracellular alpha-syn aggregation, therefore we hypothesize that a similar mechanism might lead to alpha-syn pathology propagation. |
Databáze: |
MEDLINE |
Externí odkaz: |
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