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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >JIP1-Mediated JNK Activation Negatively Regulates Synaptic Plasticity and Spatial Memory
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JIP1-Mediated JNK Activation Negatively Regulates Synaptic Plasticity and Spatial Memory

机译:JIP1介导的JNK激活负调节突触可塑性和空间记忆

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摘要

The c-Jun N-terminal kinase (JNK) signal transduction pathway is implicated in learning and memory. Here, we examined the role of JNK activation mediated by the JNK-interacting protein 1 (JIP1) scaffold protein. We compared male wild-type mice with a mouse model harboring a point mutation in the Jip1 gene that selectively blocks JIP1-mediated JNK activation. These male mutant mice exhibited increased NMDAR currents, increased NMDAR-mediated gene expression, and a lower threshold for induction of hippocampal long-term potentiation. The JIP1 mutant mice also displayed improved hippocampus-dependent spatial memory and enhanced associative fear conditioning. These results were confirmed using a second JIP1 mutant mouse model that suppresses JNK activity. Together, these observations establish that JIP1-mediated JNK activation contributes to the regulation of hippocampus-dependent, NMDAR-mediated synaptic plasticity and learning.
机译:C-JUM N-末端激酶(JNK)信号转导通路涉及学习和记忆。 在这里,我们检查了JNK相互作用蛋白1(JIP1)支架蛋白介导的JNK激活的作用。 我们将雄性野生型小鼠与含有JIP1基因中的点突变的小鼠模型进行了比较,选择性地阻断JIP1介导的JNK活化。 这些雄性突变小鼠表现出增加的NMDAR电流,增加的NMDAR介导的基因表达,以及诱导海马长期增强的阈值。 JIP1突变小鼠还显示出改善的海马依赖的空间记忆和增强的联想恐惧调节。 使用抑制JNK活性的第二JIP1突变小鼠模型来确认这些结果。 这些观察结果共同建立了JIP1介导的JNK激活有助于调节海马依赖性,NMDAR介导的突触塑性和学习。

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