Parkin suppresses wild-type α-synuclein-induced toxicity in SHSY-5Y cells

被引:31
|
作者
Oluwatosin-Chigbu, Y
Robbins, A
Scott, CW
Arriza, JL
Reid, JD
Zysk, JR
机构
[1] AstraZeneca Pharmaceut LP, Dept Mol Sci, Wilmington, DE 19850 USA
[2] AstraZeneca Pharmaceut LP, Dept Lead Discovery, Wilmington, DE 19850 USA
关键词
Parkin; alpha-synuclein; Parkinson's disease; synucleopathies; adenoviral gene delivery; dopaminergic cell line;
D O I
10.1016/j.bbrc.2003.08.059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current hypotheses concerning the mechanism of neuronal cell death in Parkinson's disease (PD) and related synucleopathies propose a functional interaction between parkin and a-synuclein (alphaS). Recently parkin was shown to suppress mutant alphaS-induced toxicity in primary neurons, providing a basis for an association between these proteins and neuronal loss [Neuron 36 (2000) 10071019]. We have asked if a similar association could be made between wild-type (wt) aS and parkin. We examined inducible overexpression of alphaS in SHSY-5Y cells through adenoviral infection under conditions which produce cellular toxicity through a reduction in ATP levels. We demonstrate that parkin suppresses toxicity induced by mutant (A53T) and wt ccS. Parkin over-expression was also associated with the appearance of higher molecular weight alphaS-immunoreactive bands by Western blot analysis. These data, consistent with a protective role for parkin, extend previous findings to include a functional association between parkin and the wt form of aS. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:679 / 684
页数:6
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