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JNK磷酸化Bad在脑缺血神经元凋亡中的作用
引用本文:王晓天,刘晓梅,尤红娟,李小翠,秦苏萍,汤仁仙,宋远见.JNK磷酸化Bad在脑缺血神经元凋亡中的作用[J].中国现代医生,2014(31):1-3.
作者姓名:王晓天  刘晓梅  尤红娟  李小翠  秦苏萍  汤仁仙  宋远见
作者单位:徐州医学院病原生物学与免疫学教研室,江苏徐州221002
基金项目:国家自然科学基金资助项目(81371300)
摘    要:目的探讨JNK磷酸化Bad在大鼠缺血性神经元凋亡中的作用。方法 20只大鼠均分为4组:假手术组、缺血复灌组、溶剂对照组和SP600125组。制作大鼠全脑缺血模型,应用免疫沉淀和免疫印迹法检测大鼠脑缺血复灌1 d海马CA1区神经元Bad与14-3-3及Bad与Bcl-Xl的结合、Bad丝氨酸128位磷酸化p-Bad(S128)]水平、Caspase-3蛋白表达情况。结果与缺血复灌组相比,SP600125组海马CA1区神经元Bad与14-3-3的结合明显增高,Bad与Bcl-Xl的结合、p-Bad(S128)、Caspase-3表达显著减少(均P〈0.05)。结论 JNK介导的Bad(S128)磷酸化在大鼠缺血性脑损伤中发挥了重要作用。

关 键 词:Bad  JNK丝裂原活化蛋白激酶类  凋亡  脑缺血

Effects of Bad phosphorylation induced by JNK on cerebral ischemic neuronal apoptosis
Authors:WANG Xiaotian  LIU Xiaomei  YOU Hongjuan  LI Xiaocui  QIN Suping  TANG Renxian  SONG Yuanjian
Institution:(Department of Pathogenic Biology and Immunology, Xuzhou Medical College, Xuzhou 221002, China)
Abstract:Objective Investigate the effects of Bad phosphorylation induced by JNK on cerebral ischemic neuronal apoptosis in rats. Methods Twenty rats were divided into 4 groups averagely: sham operation group, ischemia-reperfusion group, sol- vent control group and SP600125 group. Making rat model of cerebral ischemia, the binding of Bad and 14-3-3 ,the binding of Bad and Bcl-X1, Bad phosphorylation at serine 128(p-Bad(S128)) and Caspase-3 protein expression in hippocampal CA1 region were detected by immunoprecipitation (IP) and immunoblotting (IB) ld after isehemia-reperfusion. Results Compared with the isehemia-reperfusion group, the binding of Bad and 14-3-3 was increased, the binding of Bad and Bcl-X1, p-Bad (S128) and Caspase-3 protein expression in hippocampal CA1 region were decreased in SP600125 group (All P〈0.05). Conclu- sion Bad phosphorylation at serine 128 induced by JNK playe important effects on cerebral ischemic neuronal apoptosis in rats.
Keywords:Bad  JNK mitogen-activated protein kinases  Apoptosis  Cerebral ischemia
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