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格尔德霉素抑制Fas信号通路并保护神经元免受缺血损伤。

Geldanamycin inhibits Fas signaling pathway and protects neurons against ischemia.

作者信息

Yin Xiao-Hui, Han Yan-Ling, Zhuang Ying, Yan Jing-Zhi, Li Chong

机构信息

Jiangsu Key Laboratory of Brain Disease Bioinformation and the Research Center for Biochemistry and Molecular Biology, Xuzhou Medical University, 209 Tongshan Road, Xuzhou 221004, Jiangsu, PR China.

Jiangsu Key Laboratory of Brain Disease Bioinformation and the Research Center for Biochemistry and Molecular Biology, Xuzhou Medical University, 209 Tongshan Road, Xuzhou 221004, Jiangsu, PR China.

出版信息

Neurosci Res. 2017 Nov;124:33-39. doi: 10.1016/j.neures.2017.05.003. Epub 2017 May 15.

Abstract

The inhibitor of Heat shock proteins 90, geldanamycin (GA), has been reported neuroprotective against both global and focal brain ischemia. To understand the mechanisms underlies the neuroprotection effect of GA, we investigated the relationship between GA pretreatment and Fas signaling pathway in rat global brain ischemia/reperfusion model in the present study. Results showed that GA attenuated neuron loss significantly in hippocampal CA1 region. Upon GA pretreatment, Mixed Lineage Kinase 3 (MLK3) expression and activation and FasL expression was decreased, the assembly of death-inducing signaling complex and activation of downstream apoptosis-associating proteins were inhibited along with neuroprotection. Based on the facts that MLK3 is one client protein of HSP90 and MLK3 pathway induces FasL expression in ischemic brain injury, our study suggests one of the mechanisms of neuroprotection against brain ischemia from GA.

摘要

热休克蛋白90抑制剂格尔德霉素(GA)已被报道对全脑和局灶性脑缺血均具有神经保护作用。为了解GA神经保护作用的潜在机制,我们在本研究中调查了大鼠全脑缺血/再灌注模型中GA预处理与Fas信号通路之间的关系。结果显示,GA显著减轻了海马CA1区的神经元损失。GA预处理后,混合谱系激酶3(MLK3)的表达和激活以及FasL的表达均降低,死亡诱导信号复合物的组装和下游凋亡相关蛋白的激活受到抑制,同时伴有神经保护作用。基于MLK3是HSP90的一个客户蛋白且MLK3通路在缺血性脑损伤中诱导FasL表达这一事实,我们的研究提示了GA对脑缺血具有神经保护作用的机制之一。

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