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Cdk5/p35对于运动协调和小脑可塑性是必需的。

Cdk5/p35 is required for motor coordination and cerebellar plasticity.

作者信息

He Xiaojuan, Ishizeki Masato, Mita Naoki, Wada Seitaro, Araki Yoshifumi, Ogura Hiroo, Abe Manabu, Yamazaki Maya, Sakimura Kenji, Mikoshiba Katsuhiko, Inoue Takafumi, Ohshima Toshio

机构信息

Laboratory for Molecular Brain Science, Department of Life Science and Medical Bioscience, Waseda University, Tokyo, Japan.

出版信息

J Neurochem. 2014 Oct;131(1):53-64. doi: 10.1111/jnc.12756. Epub 2014 May 28.

Abstract

Previous studies have implicated the role of Purkinje cells in motor learning and the underlying mechanisms have also been identified in great detail during the last decades. Here we report that cyclin-dependent kinase 5 (Cdk5)/p35 in Purkinje cell also contributes to synaptic plasticity. We previously showed that p35(-/-) (p35 KO) mice exhibited a subtle abnormality in brain structure and impaired spatial learning and memory. Further behavioral analysis showed that p35 KO mice had a motor coordination defect, suggesting that p35, one of the activators of Cdk5, together with Cdk5 may play an important role in cerebellar motor learning. Therefore, we created Purkinje cell-specific conditional Cdk5/p35 knockout (L7-p35 cKO) mice, analyzed the cerebellar histology and Purkinje cell morphology of these mice, evaluated their performance with balance beam and rota-rod test, and performed electrophysiological recordings to assess long-term synaptic plasticity. Our analyses showed that Purkinje cell-specific deletion of Cdk5/p35 resulted in no changes in Purkinje cell morphology but severely impaired motor coordination. Furthermore, disrupted cerebellar long-term synaptic plasticity was observed at the parallel fiber-Purkinje cell synapse in L7-p35 cKO mice. These results indicate that Cdk5/p35 is required for motor learning and involved in long-term synaptic plasticity.

摘要

以往的研究表明浦肯野细胞在运动学习中发挥作用,并且在过去几十年里其潜在机制也已得到详细阐明。在此我们报告,浦肯野细胞中的细胞周期蛋白依赖性激酶5(Cdk5)/p35也有助于突触可塑性。我们先前表明,p35基因敲除(p35 KO)小鼠在脑结构上表现出细微异常,且空间学习和记忆受损。进一步的行为分析表明,p35 KO小鼠存在运动协调缺陷,这表明Cdk5的激活剂之一p35与Cdk5可能在小脑运动学习中起重要作用。因此,我们构建了浦肯野细胞特异性条件性Cdk5/p35基因敲除(L7-p35 cKO)小鼠,分析了这些小鼠的小脑组织学和浦肯野细胞形态,通过平衡木和转棒试验评估它们的表现,并进行电生理记录以评估长期突触可塑性。我们的分析表明,浦肯野细胞特异性缺失Cdk5/p35不会导致浦肯野细胞形态改变,但会严重损害运动协调能力。此外,在L7-p35 cKO小鼠的平行纤维-浦肯野细胞突触处观察到小脑长期突触可塑性受到破坏。这些结果表明,Cdk5/p35是运动学习所必需的,并参与长期突触可塑性。

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