Apoptosis signal-regulating kinase 1 (Ask1) targeted small interfering RNA on ischemic neuronal cell death

被引:27
|
作者
Kim, Hyun-Woo [1 ]
Cho, Kyoung-Joo [1 ]
Lee, Su Kyoung [1 ]
Kim, Gyung W. [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Neurol, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
Stroke; Cerebral infarction; Apoptosis signal-regulating kinase 1; RNA interference; Mice; FOCAL CEREBRAL-ISCHEMIA; SUBSEQUENT DNA FRAGMENTATION; MITOCHONDRIAL CYTOCHROME-C; ACTIVATED PROTEIN-KINASE; RAT HIPPOCAMPUS; OXIDATIVE STRESS; EARLY RELEASE; MICE; PATHWAYS; INJURY;
D O I
10.1016/j.brainres.2011.07.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Apoptosis signal-regulating kinase 1 (Ask1) is one of mitogen-activated protein kinase kinase kinase (MAPKKK) for cell differentiation and apoptosis. The aim of the present study is to evaluate whether RNA interference against Ask1 (Ask1-siRNA) down-regulates the expression of Ask1 and prevents apoptotic neuronal cell death after ischemia/reperfusion (I/R) in mice. Mice were subjected to intraluminal suture occlusion of the middle cerebral artery for 1 h, followed by reperfusion. The Ask1-siRNA or a control-siRNA was introduced using osmotic pump intracerebroventricularly at 3 days before I/R. The expression and mRNA of Ask1 were evaluated by Western blot and RT-PCR after I/R with time. Immunohistochemistry and TUNEL assay were also investigated to evaluate the effect of Ask1 on cerebral infarction by Ask1-siRNA treatment. The expression of Ask1 was increased significantly at 8 h after I/R. The level of mRNA and protein of Ask1 down-regulated after treatment of Ask1-siRNA and subsequently cerebral infarction volume was reduced. Our results suggest the increased Ask1 expression induce apoptotic cell death after I/R. And we also demonstrated that Ask1-siRNA attenuates upregulation of Ask1, which was followed by the reduction of infarction in ischemic brain after I/R. Ask1-siRNA could represent a molecular target for prevention of ischemic stroke. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:73 / 78
页数:6
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