کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6261882 | 1613265 | 2013 | 5 صفحه PDF | دانلود رایگان |

α-Synuclein (α-syn) is a presynaptic protein that is widely implicated in the pathophysiology of Parkinson's disease (PD). Recently, four α-syn isoforms that are produced by alternative splicing have been described, they are α-syn140, α-syn126, α-syn112, and α-syn98. The stable cell lines which expressed the four α-syn isoforms respectively were obtained, and the aggregation formation of these α-syn isoforms and their associated toxicity to PC12 cell were investigated. The results of this study indicate that over-expression of α-syn isoforms alone in dopaminergic cells have no effect on the formation of α-syn oligomeric species and cell viabilities. When exposed to rotenone, these cell lines which over expressed exon 5-lacking form of α-syn isoforms showed the formation of oligomeric species and toxicity to PC12 cells.
Highlights⺠The stable cell lines which over-expressed the four α-syn isoforms were obtained. ⺠There were no α-syn oligomeric species emergence in these four stable cell lines. ⺠There were no obvious differences in the cell viabilities of these four cell lines. ⺠The cells which expressed α-syn, deletion of exon 5, were susceptibility to rotenone. ⺠And formation of oligomeric species and decreased cell viabilities were observed.
Journal: Brain Research Bulletin - Volume 90, January 2013, Pages 127-131