Small interfering RNA targeting the PINK1 induces apoptosis in dopaminergic cells SH-SY5Y

被引:143
作者
Deng, H
Jankovic, J
Guo, Y
Xie, WJ
Le, WD [1 ]
机构
[1] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA
[2] Cent S Univ, Sch Med Technol & Informat, Changsha, Peoples R China
关键词
RNAi; PINK1; SH-SY5Y cells; apoptosis; parkinsonism;
D O I
10.1016/j.bbrc.2005.09.178
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
PTEN-induced kinase 1 (PINKJ) is a recently identified gene, mutations of which cause levodopa-responsive parkinsonism. An overexpression of wild-type PINK1 protects neurons from stress-induced mitochondrial dysfunction and apoptosis. We studied the effects of PIAIK1 suppression using small interfering RNA (siRNA), which call inhibit PINK1 mRNA expression up to 87%,, and decrease PINKI protein up to 80% in human dopaminergic cell line SH-SY5Y. Incubation with PINKI siRNA decreased SH-SY5Y cell viability and significantly increased MPP+ or rotenone-induced cytotoxicity. Our results indicate that reduction in PINK1 expression call trigger apoptotic process that can be exacerbated by the presence of MPP+ or rotenone. These findings support the hypothesis that PINK1 participates in the protection of dopaminergic neurons. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1133 / 1138
页数:6
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