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

机译:凋亡信号调节激酶1(Ask1)针对缺血性神经元细胞死亡的小干扰RNA。

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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 1h, followed by reperfusion. The Ask1-siRNA or a control-siRNA was introduced using osmotic pump intracerebroventricularly at 3days 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 8h 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.
机译:凋亡信号调节激酶1(Ask1)是一种促分裂原激活的蛋白激酶激酶激酶(MAPKKK),用于细胞分化和凋亡。本研究的目的是评估RNA干扰Ask1(Ask1-siRNA)是否下调小鼠缺血/再灌注(I / R)后Ask1的表达并防止凋亡神经元细胞死亡。对小鼠进行大脑中动脉的腔内缝合闭塞1h,然后再灌注。在I / R前3天,使用脑室内渗透泵引入Ask1-siRNA或对照-siRNA。 I / R后随时间通过蛋白质印迹和RT-PCR评估Ask1的表达和mRNA。还研究了免疫组织化学和TUNEL测定法,以评估Ask1-siRNA治疗对Ask1对脑梗死的影响。 I / R后8h,Ask1的表达明显增加。治疗后,Ask1-siRNA降低了Ask1的mRNA和蛋白水平,从而降低了脑梗死体积。我们的结果表明增加的Ask1表达可导致I / R后凋亡细胞死亡。并且我们还证明了Ask1-siRNA减弱了Ask1的上调,随后是I / R后缺血性脑梗塞的减少。 Ask1-siRNA可能代表预防缺血性中风的分子靶标。

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